Treatment of decrease in desire to eat with Unani medicine Safoof Hazim Kalan
- Conditions
- Anorexia,
- Registration Number
- CTRI/2023/01/048981
- Lead Sponsor
- Central Council for Research in Unani Medicine (CCRUM), New Delhi
- Brief Summary
This study is designed as a single centric open trial in patients with Zof e lshteha (Anorexia). After screening, patients will be enrolled if they satisfy inclusion and exclusion criteria. The patients will be assessed clinically on 7th and 14th day. This includes subjective assessment of general well being and physical examination . The total duration of treatment will be 2 weeks. Laboratory parameters for safety assessment will be conducted at baseline and on completion of the protocol therapy.
**Composition of Safoof Hazim Kalan**
| | | |
| --- | --- | --- |
|**S.No.**
**Ingredients**
**Quantity**
|1.
Post Halela Zard
20g
|2.
Post Balela
20g
|3.
Aamla
20g
|4.
Badiyan
20g
|5.
Nankhwah
20g
|6.
Zeera Safaid
20g
|7.
Namak-E-Sang
20g
|8.
Namak Siya
20g
|9.
Namak Hindi
20g
|10.
Jawakhar
20g
|11.
Tankar Biryan
10g
|12.
Naushadar
10g
|13.
Filfil Siyah
10g
|14.
Dana Heel Khurd
10g
|15.
Zanjabeel
10g
|16.
Filfil Daraz
10g
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- All
- Target Recruitment
- 110
- Patients of any sex in the age group 18-65 years.
- Patients having Zof e lshteha(Anorexia) with SNAQ score≤14.
- Patients having Anorexia nervosa 2.
- Patients having any systemic disease,chronic debilitating disease,T.B.,Diabetes Mellitus etc.
- Known cases of Hepatic,Renal or Cardiac Ailments 4.
- History of hypersensitivity to study drug or any of its ingredients.
- History of addiction (Alcohol,Drugs) 6.
- Pregnant and lactating women.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Improvement in sign and symptoms of Zof e lshteha (Anorexia) on the basis of improvement in the appetite for which the Simplified Nutritional Appetite Questionnaire (SNAQ) On baseline, 7th day and 14th day
- Secondary Outcome Measures
Name Time Method Haematological and biochemical assessment for safety assessment At baseline and end of the treatment i.e. 14th day
Trial Locations
- Locations (1)
Regional Research Institute of Unani Medicine (RRIUM), Aligarh
🇮🇳Aligarh, UTTAR PRADESH, India
Regional Research Institute of Unani Medicine (RRIUM), Aligarh🇮🇳Aligarh, UTTAR PRADESH, IndiaDr Rashid ul IslamPrincipal investigator9897975161waytorashid@gmail.com