Laparoscopic Supracervical Hysterectomy Versus Total Laparoscopic Hysterectomy
Withdrawn before enrolling · Phase 3
Conditions studied: Gynecologic Diseases
In brief
The purpose of this research study is to evaluate whether there is any difference in recovery time and return to normal activities following a laparoscopic supracervical hysterectomy (LSH) compared with total laparoscopic hysterectomy (TLH). Both types of hysterectomies are commonly performed at our institution. Patients will be assigned by chance (like a coin toss) to have either a LSH or a TLH. Preoperatively, participants will complete a quality of life questionnaire (SF-36), a sexual function questionnaire (FSFI)and a 3 question questionnaire about urinary function (3IQ). Following surgery participants will be asked to keep a diary of pain symptoms and use of narcotics. The diary will be filled out daily until patients have resumed normal activities from prior to the surgery. The SF-36 will be completed again 6 weeks following the original surgery. 6 months following surgery participants will receive a copy of the SF-36 and the FSFI in the mail. They will also be asked questions about urinary symptoms and persistent vaginal bleeding.
Key facts
- Study ID
- NCT00734812
- Run by
- Brigham and Women's Hospital
- People needed
- 0
- Starts
- 2008-05-01
- Expected to finish
- 2012-01-01
- Last updated by the study team
- 2013-01-24
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- Candidates for laparoscopic hysterectomy for benign indications
You may not qualify if…
- Malignancy of the uterus, cervix or adnexa
- pre-malignant changes of the uterus, cervix or adnexa
- history of severe cervical dysplasia (CIN II or above)
Where it is running
- Brigham and Women's Hospital — Boston, Massachusetts, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.