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A clinical trial of ayurvedic procedure with ayurvedic formulations in the management of yonibhramsha w.s.r. to pelvic organ prolapse.

A randomised comparative clinical study to evaluate the efficacy of triphaladi churna yoni pottali and mrunaladi tail yoni pichu along with udumbara palasha tail matra basti in the management of yonibhramsha.

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/07/054742
Enrollment
40
Registered
2023-07-04
Start date
Unknown
Completion date
Unknown
Last updated
2023-07-25

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

Conditions

Health Condition 1: N81- Female genital prolapse

Interventions

None listed

Sponsors

National Institute of AyurvedaJaipur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients complaining of Yoni-bhramsha having any two of the following symptoms. ï?· Patient clinically diagnosed 1st, 2nd and 3rd degree uterine prolapse associated with or without cystocele and rectocele. ï?· Patient with complaints of vaginal discharge, feeling of heaviness in genital region, disturbances in micturition, low back pain, constipation, lower abdominal pain, lack of sexual satisfaction. 2. Patients of age group 25-65 years

Exclusion criteria

Exclusion criteria: 1. Patient having only cystocele and rectocele. 2. Pregnant women. 3. Patient with decubitus ulcer. 4. Patient with chronic and metabolic disorder like diabetes mellitus, bronchial asthma, lung disease, tuberculosis, hypertension, muscular dystrophy, severe anaemia, jaundice, skin disorder etc. 5. Patient with genital tract infection i.e., pelvic inflammatory diseases, cervicitis, HBsAg, HIV, etc., or who are under treatment of same. 6. Patient having any benign and malignant growth of genital tract like Bartholin cyst, polyp, fibroid, Gartnerâ??cyst, carcinomatous growth etc. 7. Psychologically unstable patient. 8. Patient with any history of allergy. 9. Patient with any surgical history of the genital tract.

Design outcomes

Secondary

MeasureTime frame
Changes in pelvic relaxation questionnaire and associated features.Timepoint: 2 MONTHS

Primary

MeasureTime frame
1.Changes in POP-Q-SCALETimepoint: 2 MONTHS

Countries

India

Contacts

Public ContactDr Neeraja Tiwari

National Institute of Ayurveda, Jaipur

baruhunt@gmail.com9492047131

Outcome results

None listed

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