Effect of a unani formulation in the treatment of Shara (hives)
Not Applicable
Not yet recruiting
- Conditions
- Health Condition 1: L509- Urticaria, unspecified
- Registration Number
- CTRI/2022/10/046562
- Lead Sponsor
- Department of Ilmul Advia
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Clinically diagnosed patients of CU according to the 2018 EAACI/GA2LEN/EDF/WAO guideline
2. Patients willing to sign consent form for the study.
Exclusion Criteria
1. Patients less than 14 and more than 60 years of age.
2. concomitant skin disease.
3. Patients suffering from any other systemic diseases, pregnant and lactating women.
4. unwillingness or inability to fulfil the protocol.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method DECLINE IN WHEALS EPISODES AND ITCHING INTENSITYTimepoint: EVERY FORTNIGHT UPTO 6 WEEKS
- Secondary Outcome Measures
Name Time Method IMPROVEMENT IN OBJECTIVE PARAMETERS LIKE QoL QUESTIONNAIRE, UAS7 AND BLOOD REPORTSTimepoint: BEFORE AND AFTER STUDY