Vaginal Vault Prolapse Clinical Trial
Official title:
Prophylactic Modified McCall Culdoplasty During Total Laparoscopic Hysterectomy
Verified date | April 2017 |
Source | University of North Carolina, Chapel Hill |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to assess the feasibility of performing prophylactic McCall
culdoplasty at the time of total laparoscopic hysterectomy. The investigators will also be
measuring pelvic support (using POP-Q) and sexual function before and at different time
points (up to 12 months) postoperatively.
The investigators hypothesize that women undergoing the McCall culdoplasty will not have
different immediate surgical outcomes (operative time, etc) and may have better pelvic
support and sexual function in the future.
Status | Completed |
Enrollment | 50 |
Est. completion date | December 2014 |
Est. primary completion date | June 2014 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years to 99 Years |
Eligibility |
Inclusion Criteria: - Women aged 18-99 undergoing elective laparoscopic hysterectomy for benign indications with surgeons in the division of Advanced Laparoscopy and Pelvic Pain at UNC-Chapel Hill. Exclusion Criteria: - Current symptomatic or asymptomatic pelvic organ prolapse as measured by the Pelvic Organ Prolapse Quantification (POPQ) system. - Pregnancy - Non-English speaking - Unable to provide informed consent - Pathology causing an obliterated cul-de-sac |
Country | Name | City | State |
---|---|---|---|
United States | University of North Carolina at Chapel Hill | Chapel Hill | North Carolina |
Lead Sponsor | Collaborator |
---|---|
University of North Carolina, Chapel Hill |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Feasibility | The primary aim of the study is to generate feasibility data for performing a powered randomized trial on prophylactic modified McCall's culdoplasty during benign total laparoscopic hysterectomy. As such, we will measure operative time with the hypothesis that the intervention does not add significant additional effort. We will also collect information regarding patient willingness to participate as well as intra- and post-operative complication data. | 6 months | |
Secondary | Pelvic support | This study will also allow us to collect data regarding differences in POP-Q exams up to 12 months after surgery. | 12 months | |
Secondary | Sexual function | We will also collect data regarding sexual function at different time points pre and postoperatively up to 12 months after surgery using the validated Female Sexual Function Index (FSFI) questionnaire. | 12 months |
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