Health Condition 1: N814- Uterovaginal prolapse, unspecified
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: PATIENTS HAVING AGE GROUP FROM 30 TO 55 YEARS PATIENTS HAVING FIRST AND SECOND DEGREE UTERINE PROLAPSE PATIENTS HAVING FIRST DEGREE UTERINE PROLAPSE WITH CYSTOCELE OR RECTOCELE PATIENTS HAVING CLINICAL SIGN AND SYMPTOMS OF UTERINE PROLAPSE PATIENTS WILLING TO PARTICIPATE IN TRIAL
Exclusion criteria
Exclusion criteria: PATIENTS BELOW AGE OF 30 YEARS AND ABOVE AGE OF 55 YEARS PATIENTS HAVING THIRD DEGREE UTERINE PROLAPSE PREGNANCY CASES PATIENT HAVING CERVIX AND UTERINE MALIGNANCY PATIENTS HAVING PROCIDENTIA WITH DECUBITUS ULCER OR VAULT PROLAPSE PATIENTS WITH CONGENITAL PROLAPSE OR ELONGATION OF CERVIX PATIENTS HAVING RECTAL PROLAPSE OR PELVIC INFLAMMATORY DISEASE PATIENT PRESENTED WITH KNOWN CASE OF SEXUALLY TRANSMITTED DISEASE FIBROID POLYP
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| IMPROVEMENT IN SIGN AND SYMPTOMS AND CHANGES IN ASSOCIATED CLINICAL FEATURES RELATED TO UTERINE PROLAPSETimepoint: FOLLOW UP WILL BE DONE ON 8TH 14TH 30TH 38TH 44TH 60TH 68TH 74TH 90TH DAY | — |
Primary
| Measure | Time frame |
|---|---|
| IMPROVEMENT IN QUANTITATIVE GRADING OF POP FOR UTERINE PROLAPSETimepoint: FOLLOW UP WILL BE DONE ON 30TH 60TH 90TH DAY | — |
Countries
India
Contacts
INSTITUTE FOR AYURVED STUDIES AND RESEARCH