To evaluate the Safety and efficacy of Unani formulations in the treatment of Anorexia
- Conditions
- Anorexia, Zof al-IshtihÄ (Anorexia),
- Registration Number
- CTRI/2015/02/005591
- Lead Sponsor
- Central Council for Research in Unani MedicineCCRUM
- Brief Summary
This study is designed as a multicentric open trial in patients with **Khafaqan (Palpitation)** After screening, Patients will be enrolled if they satisfy inclusion and exclusion criteria. The patients will be assessed clinically every week. This includes subjective assessment of general well being and physical examination . The total duration of treatment will be 04 weeks. . Laboratory parameters for safety assessment will be conducted at baseline, first follow up and on completion of the protocol therapy.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- All
- Target Recruitment
- 300
•Patients of either sex in the age group of 18-65 •Decreased Appetite with SNAQ ≤ 14.
•Patients having Anorexia nervosa •Patients with disorders requiring long term treatment •Known cases of Hepatic, Renal or Cardiac Ailments •History of addictions (Alcohol, Drugs) •Pregnant and lactating women.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Improvement in signs and symptoms 2 weeks
- Secondary Outcome Measures
Name Time Method Hematological and biochemical assessments for safety 2 weeks
Trial Locations
- Locations (3)
Clinical Research Unit
🇮🇳Meerut, UTTAR PRADESH, India
Clinical Research Unit, Kurnool
🇮🇳Kurnool, ANDHRA PRADESH, India
Regional Research Institute of Unani Medicine, Bhadrak
🇮🇳Bhadrak, ORISSA, India
Clinical Research Unit🇮🇳Meerut, UTTAR PRADESH, IndiaDR MOHD TARIQ KHANPrincipal investigator09012843253doctormtk@gmail.com