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Treatment of whitish or yellowish vaginal discharge with Unani Medicine Kushta-i-Sadaf

Clinical Validation of Unani Pharmacopoeial Formulation Kushta-i-Sadaf in Sayalan al-Rahim due to Sue Mizaj Sada (Non-specific leucorrhoea) - leucorrhoea

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/07/091259
Enrollment
110
Registered
2025-07-21
Start date
Unknown
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Health Condition 1: N89- Other noninflammatory disorders ofvagina

Interventions

Intervention1: Kushta-i-Sadaf: 200 mg twice in a day with water after meals for 04 weeks (28 days). Control Intervention1: NIL: NIL

Sponsors

Central Council for Research in Unani Medicine CCRUM New Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All women complaining of excessive white discharge with or without any of the following associated symptoms: 1. Waja al-Zahr (Backache) 2. Naqahat (General Weakness) 3. Burning Micturition 4. Pruritus vulvae

Exclusion criteria

Exclusion criteria: 1. Age below 15 & above 49 years 2. Patient with severe anemia (Hb % Equal or less than 8gm) 3. Known cases of uterine fibroid, prolapse, malignancy and ovarian tumour or cyst 4. Patients on oral contraceptive pills (OCPs)/Intrauterine devices (IUDs)/ Hormonal Replacement Therapy (HRT) 5. Known cases of sexually transmitted diseases 6. Patients on long-term medications for systemic illnesses 7. Any abnormal condition on p/s Examination 8. Patients having acute / acute on chronic/ Chronic PID as per CDC Criteria. 9. Pregnant and Lactating women.

Design outcomes

Primary

MeasureTime frame
The efficacy of the Habb -e- Leemun in the treatment of Niqris (Chronic Gout) will be carried out on the basis of Pain (VAS-Visual Analogue Scale) and Gout Assessment Questionnaire. Timepoint: At baseline and at the end of treatment. i.e, 0 & 4th week

Secondary

MeasureTime frame
Haematological and biochemical investigations for safety assessment i.e., Hemogram,LFT, KFT, Urine Examination: Routine & Microscopic.Timepoint: At baseline and at the end of treatment. i.e, 0 & 4th week

Countries

India

Contacts

Public ContactDr Pradeep Kumar

Central Council for Research in Unani Medicine (CCRUM)

javed.ghazal@gmail.com09811810454

Outcome results

None listed

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