The
Clinical Evaluation of Herbal Anti-malarial Medicine:
SCAT
..........................................................................................................................
Khan Usmanghani, Afzal
Ahmed, Halima Nazar, Ejaz Mohuddin, Muhammad Sakhi
Sarwar
Department of Medicine & Allied Sciences,
Department of Basic Clinical Sciences, Faculty
of Eastern Medicine, Shifa-UL-Mulk Memorial Hospital
Hamdard University, Karachi, Pakistan
Address correspondence to:
Khan Usmanghani, ugk@yahoo.com
..........................................................................................................................
|
ABSTRACT
The
open, clinical, randomized trial has been
carried out on the designed, proprietary
clinically and proven different anti-malarial
medicines to analyze their efficacy and
side effects. A random controlled clinical
trial was conducted to quantify the effect
of coded herbal formulation SCAT with Qurs
Bukhareen, Qurs Humma Jadeed and Amodiaquine
ain endemic areas of Bund Murad near Hamdard
University, Karachi and the urban population
of Karachi. Patients at Matab Hamdard Aram
Bagh and Shifa-ul-Mulk Memorial Hospital
For Eastern Medicine were included in this
clinical study. The duration of treatment
was from January 2001 to June 2004.
The drugs were prescribed
to 264 patients categorizing them into different
agse from 10 years to 63 years. Three selected
drugs were administered to attain a successful
response to malaria, especially caused by
Plasmodium vivax and Plasmodium falciparium.
Herbal formulation SCAT was administered
to 88 patients, among them 56 patients who
were suffering from Plasmodium vivax and
32 who were suffering from Plasmodium falciparum.
In the Amodiaquine group 75 patients were
treated, with 41 of Plasmodium vivax and
34 patients from Plasmodium falciparum infected
malaria. Qurs Humma Jadeed was evaluated
on 56 patients, 42 from Plasmodium vivax
and 14 patients from Plasmodium falciparum
infected cases. Similarly Qurs Bukhareen
was given to 45 patients, 35 of Plasmodium
vivax and 10 patients screened for Plasmodium
falciparum. The response of the treatment
on symptomatology of malaria such as rigors,
bitter taste in mouth, headache, anorexia,
nausea, vomiting, malaise, myalgia, abdominal
pain, burning micturition, splenomegaly
and hepatomegaly were also analyzed.
A comparative evaluation
of the anti-malarial treatment by other
medicine shows that Unani therapy is safer
and proficient in its activity. After statistical
analysis Coded formulation SCAT was remarkably
effective for the associated malarial symptoms.
Coded formulation SCAT was more cost effective
than the other medicines. The statistical
analysis through chi-square test (p<
0.05) significantly proved the SCAT efficacy.
The statistical analysis of all the variables
conclusively proved that SCAT has furnished
overall good efficacy, more suitable and
superior for the prevention and treatment
of malaria. The clinical data generated
clearly proved that SCAT is the drug of
choice for malaria especially caused by
Plasmodium vivax and Plasmodium falciparum.
Objective :
To evaluate the efficacy and side effects
of herbal coded medicine "SCAT Capsule"
for the treatment of malaria along with
a comparative study of other herbal medicines
Qurs Humma Jadeed and Qurs Bukhareen, an
allopathic medicine Amodiaquine Tablet.
Aim of Study:
Malaria is a public health problem in Pakistan
and increasing trends have been observed
in the last two decades. The bulk of malaria-related
morbidity and mortality in endemic areas
like Pakistan is concentrated in children
below the age of 5 years and in pregnant
women. To reduce the risk of malarial disease
an appropriate effective curative and prophylactic
treatment is required. Herbal treatment
SCAT Capsule is an economical, safe and
effective anti-malarial treatment. The purpose
of this study was to prove the efficacy
and safety of herbal medicine.
|
Key
words: Malaria, Plasmodium vivax, Plasmodium
falciparum.
...........................................................................................................................
Malaria is a disease of the
blood that is transmitted to people by infected
mosquitoes. Malaria is very common throughout
the world. In Pakistan, the main risk is at home
and to persons traveling to tropical and subtropical
countries where malaria is more prevalent. Malaria
is caused by any one of four species of one-celled
parasites, called Plasmodium. The parasite is
spread to people by the female Anopheles mosquito,
which feeds on human blood. Although four species
of malaria parasites can infect humans and cause
illness, only malaria caused by Plasmodium falciparum
is potentially life threatening. A person gets
malaria from the bite of an infected female mosquito.
The mosquito bite injects young forms of the malaria
parasite into the person's blood. The parasites
travel through the person's bloodstream to the
liver, where they grow to their next stage of
development. In 6 to 9 days, the parasites leave
the liver and enter the bloodstream again. They
invade the red blood cells, finish growing, and
begin to multiply quickly. The number of parasites
increases until the red blood cells burst, releasing
thousands of parasites into the person's bloodstream.
The parasites attack other red blood cells, and
the cycle of infection continues, causing the
common signs and symptoms of malaria. Malaria
caused by Plasmodium falciparum can cause kidney
or liver failure, coma, and death. Although infections
with other malaria parasites cause less serious
illness, parasites can remain inactive in the
liver and cause a reappearance of symptoms months
or even years later.
The seriousness of the worldwide re-emergence
of malaria is made worse by the spread of parasites
that are resistant to anti-malaria drugs. Parasites,
like bacteria and viruses, can develop resistance
to the drugs used to prevent or treat infection.
Malaria parasites are increasingly resistant to
chloroquine, the drug most widely used for prevention
and treatment. Chloroquine-resistant strains have
been reported from areas in Africa, Asia, and
the Americas. Pakistan is anexception for drug
resistance [1]. Thus, alternative anti-malarial
drugs are needed urgently. Coded herbal formulation
SCAT Capsule has yet to be registered however
it does have anti-malarial action. Therefore,
there is a great need of a safe drug that has
less resistance with good efficacy. After an extensive
bioactivity literature search from NAPALERT data
coded herbal formulation SCAT is designed [2,3,4,
5]. SCAT Capsule is a combination of four plants
named as; Artemisia vulgaris (Afsanteen), Sisymbrium
irio (Khaksi), Tinospora cordifolia (Satgilo)
and Caesalpinea bonducela (Karanjwa).
Patients were administered drugs daily for two
weeks. The treatment groups were assigned the
following regimens: group 1, SCAT Capsule Cap
(two capsules twice daily); group 2, Amodoquine
(two tablets twice daily); group 3, Qurs Humma
Jadeed (one tablet thrice daily) and group 4,
Qurs Bukhareen (one tablet thrice daily). All
the patients then joined one of the active treatment
groups according to randomization. Randomization
was performed by the research investigator and
was from a computer-generated table of numbers
in permuted blocks of five. Patients were allocated
treatment sequentially in order of study numbers.
Comparative study between SCAT
and the other drugs such as Amodiaquine, Qurs
Humma Jadeed, and Bukhareen exhibit the anti-malarial
effects on Plasmodium vivax. A comparative evaluation
of the anti-malarial treatment by other medicine
shows that Unani therapy is safer and proficient
in its activity. After statistical analysis Coded
formulation SCAT was remarkably effective for
the associated malarial symptoms. The statistical
analysis through chi-square test (p< 0.05)
significantly proved the SCAT efficacy. In the
statistical analysis of all the variables it was
conclusively proved that SCAT has furnished overall
good efficacy, more suitable and superior for
the prevention and treatment of malaria. The clinical
data generated, clearly proved that SCAT is the
drug of choice for malaria especially caused by
Plasmodium vivax and Plasmodium falciparum.
|
Table
1. Comparative data for the complaint
of RIGORS (Plasmodium vivax)
|
|
Level
of Improvement
|
Complete
Improvement
|
Slight Improvement
|
No
Improvement
|
|
SCAT
|
87%
|
13%
|
0%
|
|
Amodiaquine
|
87%
|
13%
|
0%
|
|
Qurs Humma Jadeed
|
79%
|
17%
|
4%
|
|
Qurs Bukhareen
|
41%
|
21%
|
38%
|
|
Table
2. Comparative data for the complaint
of BITTER TASTE IN MOUTH (Plasmodium
vivax)
|
|
Level
of Improvement
|
Complete
Improvement
|
Slight Improvement
|
No
Improvement
|
|
SCAT
|
88%
|
12%
|
0%
|
|
Amodiaquine
|
81%
|
19%
|
0%
|
|
Qurs Humma Jadeed
|
81%
|
15%
|
4%
|
|
Qurs Bukhareen
|
27%
|
23%
|
50%
|
|
Table
3. Comparative data for the complaint
of HEADACHE (Plasmodium vivax)
|
|
Level
of Improvement
|
Complete
Improvement
|
Slight Improvement
|
No
Improvement
|
|
SCAT
|
70%
|
30%
|
0%
|
|
Amodiaquine
|
81%
|
19%
|
0%
|
|
Qurs
Humma Jadeed
|
86%
|
14%
|
0%
|
|
Qurs
Bukhareen
|
0%
|
44%
|
56%
|
|
Table
4. Comparative data for the complaint
of ANOREXIA (Plasmodium vivax)
|
|
Level
of Improvement
|
Complete
Improvement
|
Slight Improvement
|
No
Improvement
|
|
SCAT
|
84%
|
16%
|
0%
|
|
Amodiaquine
|
93%
|
7%
|
0%
|
|
Qurs
Humma Jadeed
|
83%
|
17%
|
0%
|
|
Qurs
Bukhareen
|
13%
|
25%
|
62%
|
|
Table
5. Comparative data for the complaint
of NAUSEA (Plasmodium vivax)
|
|
Level
of Improvement
|
Complete Improvement |
Slight Improvement
|
No
Improvement
|
|
SCAT
|
86%
|
14%
|
0%
|
|
Amodiaquine
|
93%
|
7%
|
0%
|
|
Qurs
Huma Jadeed
|
80%
|
13%
|
7%
|
|
Qurs
Bukhareen
|
24%
|
19%
|
57%
|
|
Table
6. Comparative data for the complaint
of VOMITTING (Plasmodium vivax)
|
|
Level
of Improvement
|
Complete
Improvement
|
Slight Improvement
|
No
Improvement
|
|
SCAT
|
78%
|
22%
|
0%
|
|
Amodiaquine
|
100%
|
0%
|
0%
|
|
Qurs
Humma Jadeed
|
92%
|
8%
|
0%
|
|
Qurs
Bukhareen
|
0%
|
75%
|
25%
|
|
Table
7. Comparative data for the complaint
of MYALGIA (Plasmodium vivax)
|
|
Level
of Improvement
|
Complete
Improvement
|
Slight Improvement |
No
Improvement
|
|
SCAT
|
73%
|
27%
|
0%
|
|
Amodiaquine
|
88%
|
12%
|
0%
|
|
Qurs
Humma Jadeed
|
88%
|
12%
|
0%
|
|
Qurs
Bukhareen
|
17%
|
17%
|
66%
|
|
Table
8. Comparative data for the complaint
of SWEATING (Plasmodium vivax)
|
|
Level
of Improvement
|
Complete
Improvement
|
Slight Improvement |
No
Improvement
|
|
SCAT
|
73%
|
27%
|
0%
|
|
Amodiaquine
|
88%
|
12%
|
0%
|
|
Qurs
Humma Jadeed
|
88%
|
12%
|
0%
|
|
Qurs
Bukhareen
|
17%
|
17%
|
66%
|
|
Table
9. Comparative data for the complaint
of MALAISE (Plasmodium vivax)
|
|
Level
of Improvement
|
Complete
Improvement
|
Slight Improvement
|
No
Improvement
|
|
SCAT
|
88%
|
12%
|
0%
|
|
Amodiaquine
|
83%
|
17%
|
0%
|
|
Qurs
Humma Jadeed
|
77%
|
18%
|
5%
|
|
Qurs
Bukhareen
|
35%
|
23%
|
42%
|
|
Table
10. Comparative data for the complaint
of PUFFINESS IN FACE AND LIDS (Plasmodium
vivax)
|
|
Level
of Improvement
|
Complete
Improvement
|
Slight Improvement |
No
Improvement
|
|
SCAT
|
100%
|
0%
|
0%
|
|
Amodiaquine
|
100%
|
0%
|
0%
|
|
Qurs
Humma Jadeed
|
0%
|
0%
|
0%
|
|
Qurs
Bukhareen
|
0%
|
0%
|
0%
|
|
Table
11. Comparative data for the complaint
of ABDOMINAL PAIN (Plasmodium vivax)
|
|
Level
of Improvement
|
Complete
Improvement
|
Slight Improvement |
No
Improvement
|
|
SCAT
|
57%
|
43%
|
0%
|
|
Amodiaquine
|
100%
|
0%
|
0%
|
|
Qurs
Humma Jadeed
|
50%
|
50%
|
0%
|
|
Qurs
Bukhareen
|
50%
|
0%
|
50%
|
|
Table
12. Comparative data for the complaint
of MALAISE (Plasmodium vivax)
|
|
Level
of Improvement
|
Complete
Improvement
|
Slight Improvement |
No
Improvement
|
|
SCAT
|
75%
|
25%
|
0%
|
|
Amodiaquine
|
50%
|
50%
|
0%
|
|
Qurs
Humma Jadeed
|
75%
|
25%
|
0%
|
|
Qurs
Bukhareen
|
0%
|
40%
|
60%
|
|
Table
13. Comparative data for the complaint
of RIGORS (Plasmodium falciparum)
|
|
Level
of Improvement
|
Complete
Improvement
|
Slight Improvement
|
No
Improvement
|
|
SCAT
|
97%
|
3%
|
0%
|
|
Amodiaquine
|
97%
|
3%
|
0%
|
|
Qurs
Humma Jadeed
|
71%
|
21%
|
8%
|
|
Qurs
Bukhareen
|
33%
|
33%
|
34%
|
|
Table
14. Comparative data for the complaint
of BITTER TASTE IN MOUTH (Plasmodium
falciparum)
|
|
Level
of Improvement
|
Complete
Improvement
|
Slight Improvement |
No
Improvement
|
|
SCAT
|
96%
|
4%
|
0%
|
|
Amodiaquine
|
90%
|
10%
|
0%
|
|
Qurs
Humma Jadeed
|
69%
|
23%
|
8%
|
|
Qurs
Bukhareen
|
28%
|
29%
|
43%
|
|
Table
15. Comparative data for the complaint
of HEADACHE (Plasmodium falciparum)
|
|
Level
of Improvement
|
Complete
Improvement
|
Slight Improvement |
No
Improvement
|
|
SCAT
|
96%
|
4%
|
0%
|
|
Amodiaquine
|
84%
|
16%
|
0%
|
|
Qurs
Humma Jadeed
|
63%
|
25%
|
12%
|
|
Qurs
Bukhareen
|
33%
|
50%
|
17%
|
|
Table
16. Comparative data for the complaint
of ANOREXIA (Plasmodium falciparum)
|
|
Level
of Improvement
|
Complete
Improvement
|
Slight Improvement |
No
Improvement
|
|
SCAT
|
95%
|
5%
|
0%
|
|
Amodiaquine
|
93%
|
7%
|
0%
|
|
Qurs
Humma Jadeed
|
67%
|
33%
|
0%
|
|
Qurs
Bukhareen
|
40%
|
40%
|
20%
|
|
Table
17. Comparative data for the complaint
of NAUSEA (Plasmodium falciparum)
|
|
Level
of Improvement
|
Complete
Improvement
|
Slight Improvement |
No
Improvement
|
|
SCAT
|
100%
|
0%
|
0%
|
|
Amodiaquine
|
86%
|
14%
|
0%
|
|
Qurs
Humma Jadeed
|
80%
|
20%
|
0%
|
|
Qurs
Bukhareen
|
43%
|
43%
|
14%
|
|
Table
18. Comparative data for the complaint
of VOMITING (Plasmodium falciparum)
|
|
Level
of Improvement
|
Complete
Improvement
|
Slight Improvement |
No
Improvement
|
|
SCAT
|
100%
|
0%
|
0%
|
|
Amodiaquine
|
75%
|
25%
|
0%
|
|
Qurs
Humma Jadeed
|
100%
|
0%
|
0%
|
|
Qurs
Bukhareen
|
75%
|
25%
|
0%
|
|
Table
19. Comparative data for the complaint
of MYALGIA (Plasmodium falciparum)
|
|
Level
of Improvement
|
Complete
Improvement
|
Slight Improvement |
No
Improvement
|
|
SCAT
|
100%
|
0%
|
0%
|
|
Amodiaquine
|
94%
|
6%
|
0%
|
|
Qurs
Humma Jadeed
|
67%
|
33%
|
0%
|
|
Qurs
Bukhareen
|
50%
|
25%
|
25%
|
|
Table
20. Comparative data for the complaint
of SWEATING (Plasmodium falciparum)
|
|
Level
of Improvement
|
Complete
Improvement
|
Slight Improvement |
No
Improvement
|
|
SCAT
|
97%
|
3%
|
0%
|
|
Amodiaquine
|
87%
|
13%
|
0%
|
|
Qurs
Humma Jadeed
|
69%
|
23%
|
8%
|
|
Qurs
Bukhareen
|
33%
|
44%
|
23%
|
|
Table
21. Comparative data for the complaint
of MALAISE (Plasmodium falciparum)
|
|
Level
of Improvement
|
Complete
Improvement
|
Slight Improvement |
No
Improvement
|
|
SCAT
|
97%
|
3%
|
0%
|
|
Amodiaquine
|
87%
|
13%
|
0%
|
|
Qurs
Humma Jadeed
|
67%
|
25%
|
8%
|
|
Qurs
Bukhareen
|
37%
|
38%
|
25%
|
|
Table
22. Comparative data for the complaint
of ABDOMINAL PAIN (Plasmodium falciparum)
|
|
Level
of Improvement
|
Complete
Improvement
|
Slight Improvement |
No
Improvement
|
|
SCAT
|
86%
|
14%
|
0%
|
|
Amodiaquine
|
67%
|
33%
|
0%
|
|
Qurs
Humma Jadeed
|
100%
|
0%
|
0%
|
|
Qurs
Bukhareen
|
0%
|
50%
|
50%
|
|
Table
23. Comparative data for the complaint
of BURNING MICTURITION (Plasmodium
falciparum)
|
|
Level
of Improvement
|
Complete
Improvement
|
Slight
Improvement |
No
Improvement
|
|
SCAT
|
91%
|
9%
|
0%
|
|
Amodiaquine
|
75%
|
25%
|
0%
|
|
Qurs
Humma Jadeed
|
100%
|
0%
|
0%
|
|
Qurs
Bukhareen
|
67%
|
0%
|
33%
|
Coded formulation SCAT that
was utilized in Unani Medicine was proved effective
for the treatment and prevention of parasitic
disorder like malaria caused by Plasmodium vivax
and Plasmodium falciparum. Coded formulation SCAT
also provided hepato-protective as well as spleno-protective
support. So in this context it is proved as a
safe medicine. A comparative evaluation of the
anti-malarial treatment by other medicine shows
that Unani therapy is safer and proficient in
its activity. The data presented in the dissertation
showed that Coded formulation SCAT was also effective
against malarial resistant strains and it does
not produce resistance to the treatment. After
statistical analysis Coded formulation SCAT was
remarkably effective for the associated malarial
symptoms. Coded formulation SCAT was more cost
effective then the other medicines.
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