A clinical trial to study the effects of traditional treatments in patients with pelvic organ prolapse
Phase 4
- Conditions
- Health Condition 1: null- First and second degree Uterine prolapse with or without cystocele and rectocele
- Registration Number
- CTRI/2013/04/003563
- Lead Sponsor
- Centre for Clinical Research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
Patient with age group of 35-65 yrs
First and second degree prolapse with or without cystocele and rectocele.
Willing to sign informed Consent
Willing to follow interventions like diet, exercise and life style modifications for period of 3 months
Exclusion Criteria
Any systemic illness
Pelvic inflammatory disease
Local conditions â?? Vaginitis, Cervicitis, Decubitus ulcers
Rectal prolapse
Malignancies of genital organs
Prolapse with uterine fibroids
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Improvement or cure of POP symptoms using self-report and POP Questionnaire.Timepoint: 3 months
- Secondary Outcome Measures
Name Time Method Improvement or cure in the pelvic anatomy using the POPQ system. <br/ ><br>Timepoint: 6 months