To evaluate the Safety and efficacy of Unani formulations in the treatment of Dysentery
- Conditions
- Acute amebic dysentery, DYSENTRY,
- Registration Number
- CTRI/2013/12/004262
- Lead Sponsor
- Monetary Support Central Council for Research in Unani Medicine CCRUM New Delhi
- Brief Summary
This study is designed as a multicentric open trial in patients with **Zaheer(Dysentry).** After screening, Patients will be enrolled if they satisfy inclusion and exclusion criteria. The clinical follow-up will be carried out every alternate day.This includes subjective assessment of general well being and physical examination. The total duration of treatment will be 01 week. Laboratory parameters for safety assessment will be conducted at baseline and end of study.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- All
- Target Recruitment
- 170
•Age-20-60 •Increased frequency of motion •Tenesmus •Sense of incomplete evacuation •Frequent constipation followed by diarrhoea •Loose stools with or without mucous •Associated symptoms like Nausea /Flatulence /Vomiting.
1Patients with severe loose motion more than 8 in a day 2Patients with blood in stool 3Cholera/Ulcerative colitis 4High grade fever (more than 101 ºC) 5Patient having illnesses requiring long term treatment especially DM, CRF,HT.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Improvement in signs and symptoms 1 WEEK
- Secondary Outcome Measures
Name Time Method Hematological and biochemical assessments for safety 1 WEEK
Trial Locations
- Locations (2)
CLINICAL RESEARCH UNIT
🇮🇳Meerut, UTTAR PRADESH, India
Regional Research Institute of Unani Medicine, New Delhi
🇮🇳South, DELHI, India
CLINICAL RESEARCH UNIT🇮🇳Meerut, UTTAR PRADESH, IndiaDR MOHD TARIQ KHANPrincipal investigator09012843253doctormtk@gmail.com