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To evaluate the Safety and efficacy of Unani formulation Majoon Supari paak in SayalÄ?n al-Rahim (Leucorrhoea)

Phase 2
Conditions
Health Condition 1: N898- Other specified noninflammatory disorders of vagina
Registration Number
CTRI/2015/10/006290
Lead Sponsor
Central Council for Research in Unani Medicine New Delhi
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
300
Inclusion Criteria

•Female patients in the age group of 13-45 years.

•Patients having excessive white discharge with or without any of the following associated symptoms

•Wajaâ?? al-Zahr (Backache)

•Naqahat (General Weakness)

•Faqr al-Dam (Anaemia) (8-10 mg % in females)

Exclusion Criteria

•Patients having acute/ acute on chronic/Chronic PIDs (as per the CDC Diagnostic Criteria attached as an annexure-IV)

•Patients on long-term medications.

•Patients on Oral Contraceptives/IUDs.

•Patients taking hormonal therapy.

•Any abnormal condition on p/s Examination.

•Pregnant and lactating women.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
improvement in the sign and symptoms of SayalÄ?n al-Rahim (Leucorrhoea)Timepoint: 4 weeks
Secondary Outcome Measures
NameTimeMethod
Hematological and biochemical assessments for safetyTimepoint: 4 weeks
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