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NCT ID: NCT02877407 Recruiting - Clinical trials for Uterovaginal Prolapse

Laparoscopic/Robotic-assisted Hysteropexy Versus Vaginal Hysterectomy for the Treatment of Uterovaginal Prolapse

PROLAPSE
Start date: June 2016
Phase: N/A
Study type: Interventional

- objective: aimed to compare laparoscopic/robot-assisted hysteropexy with vaginal hysterectomy for uterine prolapse - prospective randomized clinical trial - patient 1. 60yrs or more women and 2. POP-Q stage II with symptom or POP-Q III, IV regardless of symptom - number of patient: 146 - randomize: laparoscopic/robot-assisted hysteropexy vs. hysterectomy - follow up: postoperative 1 year - primary endpoint: recurrence rate 1. recurrence of uterovaginal prolapse POP-Q stage II-IV 2. recurrence of associated symptom - secondary endpoint 1. postoperative 1 year QOL, degree of satisfaction evaluation 2. operative time, estimated blood loss 3. hospitalization period, postoperative pain, return to normal activity