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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.

Phase 2
Conditions
Health Condition 1: N81- Female genital prolapse
Registration Number
CTRI/2023/07/054742
Lead Sponsor
ational Institute of AyurvedaJaipur
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
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

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.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1.Changes in POP-Q-SCALETimepoint: 2 MONTHS
Secondary Outcome Measures
NameTimeMethod
Changes in pelvic relaxation questionnaire and associated features.Timepoint: 2 MONTHS
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