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REPORT ON THE CLINICAL
TRIAL
OF
"LIVGOOD CAPSULE" IN LIVER DISORDERS
INTRODUCTION :
The LIVER is the largest gland of the body. It is situated
in the right hypochondrium. It plays a central and varied
role in many essential physiological process. The liver is
essential for life and it is the chemical factory of the
body. It may viewed as serving a regulatory and protective
functions for whole organism. To the extent of that such
biotransformation results in the formation of toxic product
as in the case of certain drugs, the liver may be bear
attack as their adverse effects. LIVER helps in all
shorts of metabolism, blood formation, bile secretion,
vitamins synthesis, heat regulation and many other
performances are generally done in all the times. So the
careful assessment is equally important in the patients with
obvious liver diseases. In this study the "LIVGOOD"
capsule was trailed in the patients of liver disorders to
know the efficiency of the drug clinically.
AIM AND OBJECT :
To evaluate the therapeutic value of "Livgood" Capsules in the patients
of liver disorders, the present clinical trial was under taken. Total 55
cases have been registered for this study. But out of these cases only 50
cases were included in the drug trial, who had followed the full treatment
schedule.
MATERIAL AND METHOD :
Total 55 patients of liver disorders were registered during the course
of trial. The study consists clinical patterns in the management of the
particulars condition with the "LIVGOOD" capsules. out of 55 cases
had followed full term (90 days) treatment schedule. The rest of the cases
had discontinued the course of treatment.
This study consisted of clinical pattern, the liver disorders and the
management of the particular condition with "Livgood" capsules.
The clinical pattern were studied in all the 55 cases for incidence of age,
sex, religion, occupation, economic status, education and social status and
symptoms of liver disorders following the incidence of L.F.T.
SELECTION OF CASES :
All the patients selected for the study were interrogated and details
history recorded in the case record form. All the patients were thoroughly
examined and findings were recorded. After the clinical examination patients
were subjected for laboratory investigation, routine examination of blood,
stool and urine were done and to establish the final diagnosis, liver
function test (L.F.T.) were done. The individual who have symptoms of liver
disorders with or without raised Bilirubin level, S.G.P.T, S.G.O.T. and
Alkaline phosphatase etc. were subjected to clinical trial.
METHODS OF DRUG
ADMINISTRATION :
The drug "Livgood" was administered in the form of capsules prepared and
supplied by "GOOD CARE PHARMA PVT. LTD., 1, Gupta Lane, kolkata - 700006.
The patients liver disorder taken for the study, were administered 2 capsule
(500 MG Each) twice daily orally morning and evening with water for a period
of 90 days.
DIET :
All the patients selected for the trial were advised to avoid butter,
ghee and spicy food.
FOLLOW UP
:
Follow up study was conducted in all cases at interval of one month for
3 months (90 days), L.F.T. was done in each cases in every month.
CLINICAL PATTERN
:
The present study consists of total 50 cases who have symptoms of liver
disorders and completed the full course
of treatment schedule (i.e., 90 days). But we had registered 55 cases for
the present study, out of which 5 cases had not completed the full course of
treatment. So the clinical pattern will be discussed on 55 cases. But the
result will be analyzed on observation of the findings of 50 cases.
Age Incidents :
Patient of the present study were from 20 to 60 years of age.
Patients of different age group are given in Table no. 1.
Table No. 1 showing the
incidence of different Age Group
|
Sl. No. |
Age Groups (years) |
No. of Patients |
Percentage |
|
1 |
21-35 |
25 |
45.45 |
|
2 |
36-50 |
24 |
43.64 |
|
3 |
51& Above |
06 |
10.91 |
|
Total |
55 |
100.00 |
Sex Incidnts
:
Patients of both sexes were registered for the present study. The
sex groups are given in Table No. 2.
Table No. 2 showing the
incidence of Sex
|
Sl. No. |
Sex |
No. of Patients |
Percentage |
|
1 |
Male |
35 |
63.63 |
|
2 |
Female |
20 |
36.37 |
|
Total |
55 |
100.00 |
Religion Incidents
:
Patients of various religions were included in this study. Patients
belonging to different religion are shown in Table No. 3.
Table No. 2 showing the
incidence of Religion
|
Sl. No. |
Religion |
No. of Patients |
Percentage |
|
1 |
Muslim |
30 |
54.54 |
|
2 |
Hindu |
20 |
36.36 |
|
3 |
Christian |
|
10.91 |
|
Total |
55 |
100.00 |
Occupation Incidents
:
In this study patients
belonging to various occupations were included and shown in Table No. 4.
Table No. 2 showing the
incidence of Occupation
|
Sl. No. |
Religion |
No. of Patients |
Percentage |
|
1 |
Service |
13 |
23.64 |
|
2 |
House-Wives |
12 |
21.82 |
|
3 |
Labour |
10 |
18.18 |
|
4 |
Cultivator |
05 |
9.09 |
|
5 |
Student |
05 |
9.09 |
|
6 |
Businessman |
08 |
14.54 |
|
7 |
Retired |
02 |
3.64 |
|
Total |
55 |
100.00 |
Educational Status
:
When educational status was enquired, patients of both literate and
illiterate were found in this series. The educational status as found are
given in Table No. 6
Table No. 2 showing
the incidence of Educational Status
|
Sl. No. |
Religion |
No. of Patients |
Percentage |
|
1 |
Illeterate |
10 |
18.18 |
|
2 |
Primary |
20 |
36.37 |
|
3 |
Madhyamik |
10 |
18.18 |
|
4 |
Higher Secendary |
04 |
7.27 |
|
5 |
Graduate |
09 |
16.36 |
|
6 |
Post Graduate |
02 |
3.64 |
|
Total |
55 |
100.00 |
Rural and urban
Incidents :
This study included patients from urban and rural areas shown in Table
no. 7.
Table No. 2
showing the incidence of Diet Habits
|
Sl. No. |
Nature of Work |
No. of Patients |
Percentage |
|
1 |
Secondary |
26 |
47.27 |
|
2 |
Moderate |
17 |
30.91 |
|
3 |
Hard worker |
12 |
21.82 |
|
Total |
55 |
100.00 |
RESULT AND OBSERVATION
:
The results of 50 patients who
had completed the treatment schedule (i.e., 90 days) were observed in terms
of subjective improvements, which are presented bellow in Table No. 10.
Table No. 2
showing the incidence of Diet Habits
|
Sl. No. |
Religion |
No. of Patients |
Percentage |
|
1 |
Service |
13 |
23.64 |
|
2 |
House-Wives |
12 |
21.82 |
|
3 |
Labour |
10 |
18.18 |
|
4 |
Cultivator |
05 |
9.09 |
|
5 |
Student |
05 |
9.09 |
|
6 |
Businessman |
08 |
14.54 |
|
7 |
Retired |
02 |
3.64 |
|
Total |
55 |
100.00 |
Incidents of
Nature of Work
:
In this trial study nature of work were studied which are presented in
Table No. 9.
Table No. 2
showing the incidence of Diet Habits
|
Sl. No. |
Nature of Work |
No. of Patients |
Percentage |
|
1 |
Sedentary |
26 |
47.27 |
|
2 |
Moderate |
17 |
30.91 |
|
3 |
Hard worker |
12 |
21.82 |
|
Total |
55 |
100.00 |
RESULT AND OBSERVATION
:
The results of 50 patients who had completed the treatment schedule
(i.e., 90 days) were observed in terms of subjective improvements, which are
presented bellow in Table No. 10.
Table No. 2
showing the response of treatment on subjective features of sexual disorder
|
Sl. No. |
Symptoms |
No. of Pt. before treatment |
No. of Pt. after
treatment |
Percentage of relief |
|
1 |
Anorexia |
50 |
42 |
84.00 |
|
2 |
Yellow Urine |
30 |
25 |
83.33 |
|
3 |
Yellow eyes / Palms |
20 |
18 |
90.00 |
|
4 |
Upper Abdominal Discomfort |
46 |
36 |
78.27 |
|
5 |
Fever |
34 |
28 |
82.36 |
|
6 |
Nausea |
32 |
25 |
78.12 |
|
7 |
Vomiting |
20 |
16 |
82.36 |
|
8 |
Loss of Weight |
42 |
21 |
50.00 |
|
9 |
Headache |
35 |
26 |
74.29 |
|
10 |
Skin Rashes |
11 |
09 |
81.82 |
|
11 |
Bleeding Nose |
08 |
06 |
75.00 |
|
12 |
Weakness |
44 |
30 |
68.18 |
|
13 |
Loss Libido |
30 |
30 |
00.00 |
In all patients
who had complete the treatment schedule of 90 (Ninety) days were also
observed in terms of objective improvements which are presented in Table No.
11.
Table No. 2 showing
the response of treatment on objective features of Liver Disorders
(Mean effects, n=50)
|
Sl. No. |
|
B.T |
A.T |
|
1 |
Serum Bilirubin Mg / d1 |
2.82 + 0.40
- |
0.90 + 0.04
- |
|
2 |
Alkaline Phosphatase |
271.09 + 10.05
- |
214.92 + 7.80
- |
|
3 |
SGOT |
104.20 + 36.97
- |
34.36 + 1.70
- |
|
4 |
SGPT |
108.47 + 38.32
- |
35.66 + 1.37
- |
|
 |
DISCUSSION:
55 patients suffering from liver disorders were included in the present
series of clinical study. The clinical study was under taken to evaluate the
efficacy, the drug "Livgood" capsule were given in these cases. Out of 55
cases 50 cases could be followed up properly.
To all the patients in the trial "Livgood" capsules was given in the dose of
2 cap (500 mg each) twice orally, morning and evening with water for a
period of 90 days. The effects of the drug on 50 patients was observed in
consideration of subjective and objective improvements. At the end of
treatment the result was assessed in terms of excellent response, good
response and poor response. The patient were included in the excellent
response group, when the objective criteria's become normal and showed 75%
relief from classical clinical features within 3 months.
The patients were included under the good response group, when they showed
more than 50% relief of subjective features and normal objective parameters.
The patients were included in poor response group when they showed less than
50% relief of subjective criteria's and negligible improvements of objective
criteria's.
When the total effects of the drug on the subjective criteria's and
subjective criteria's were taken into consideration, 28% cases were included
in excellent response group, 58% cases in good response group and 14.00% in
poor response group to the treatment in the "Livgood" capsule.
During study of the "Livgood" capsules none of the patients had shown any
side effects.
CONCLUSION:
The drug "Livgood" capsules had been found to be a hepatoprotective drug
with definite effects in the treatment of liver disorders. The results in
the trial group has shown encouraging result after 30 days of treatment.
After 90 days of the treatment the statistical data has shown the
significant response in the objective criterias like Serum Bilirubin, SGOT,
SGPT and Alkaline Phosphatase. So "Livgood" can safely be given in liver
disorders.
ACKNOWLEDGEMENT:
We sincerely acknowledge Dr. P.K.Mukherjee, Project officer and Asst.
Director (Ayurveda) for sanctioning permission to conduct the trial at IPGAE
& Research at Shyamadas Vaidyasastrapith Hospital, Kolkata - 700006. We
further acknowledge M/s Goodcare Pharma Ltd., 1, Gupta Lane, Kolkata -
700006, for their financial support for this trial.
Research
Scholar
Dr. Mofizuddin Ahmed |
Co-investigator
Dr. P.C. Tripathi
|
Principal
Investigator
Dr. B. P. Shaw
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