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Evaluating efficacy and safety of Unani drug in Sayal ?n al-Ra?im (Leucorrhoea)

A Randomized, Parallel Group, Single-Blind, Placebo Controlled Clinical Study to Evaluate Therapeutic Efficacy and Safety of Safuf Babul (Acacia arabica pods) in Sayal ?n al-Ra?im (Leucorrhoea) - N/A

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/10/058205
Enrollment
60
Registered
2023-10-03
Start date
Unknown
Completion date
Unknown
Last updated
2023-10-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: N949- Unspecified condition associated with female genital organs and menstrual cycle

Interventions

Intervention1: Safuf Phali-e-Babul (Acacia arabica pods powder): Dosage Form: Powder in Capsule Form Dose: 4 Capsules (500 mg each) orally twice daily (BD) Composition: Powder of Acacia Arabica unseed

Sponsors

National Research Institute Of Unani Medicine For Skin Disorders
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: i) Female patients in the age group of 13-45 years ii) Patients of Sayal ?n al-Ra?im (Leucorrhoea) having the following symptoms: a) Excessive white or creamy vaginal discharge evident from persistent vulvar moistness or staining of the undergarments (brownish-yellow stain on drying) or need to wear a vulvar pad, with or without any of the following associated symptoms: b) Waja‘ al-Kh ??ira (Low Backache) c) ?u’f-i-‘Am (General Weakness) d) Non-infective Leucorrhoea

Exclusion criteria

Exclusion criteria: i) Age below 13 years and above 45 years ii) Patients with Pelvic Inflammatory Disease (PID), Infective leucorrhea iii) Positive History of Venereal Disease/ Sexually Transmitted Disease (Syphilis, Gonorrhoea) iv) Patients using oral contraceptive pills (OCPs), intrauterine contraceptive device (IUCD), hormone therapy, and any long-term medications v) Significant Pulmonary/Cardiovascular/Hepato-Renal Dysfunction vi) Known cases of Immunocompromised states (HIV/ AIDS, etc.)/ Malignancies vii) Post-delivery or post-abortion period of viii) Pregnant and lactating women

Design outcomes

Primary

MeasureTime frame
Reduction in Discharge per vaginum from baseline after treatment of 6 weeks Timepoint: 42 Days

Secondary

MeasureTime frame
i) Relief in Low Backache ii) Improvement in symptoms of generalized weakness iii) Systemic Safety assessmentTimepoint: 42 Days

Countries

India

Contacts

Public ContactDr Alfiya Inayat Ansari

National Research Institute Of Unani Medicine For Skin Disorders

ccrumhqrsnd58@gmail.com8700027178

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026