Skip to main content
OpenTrials
Completed

NCT Number: NCT02696239

Vaginal Cuff Closure in Robotic Hysterectomy

The purpose of this study is to evaluate the impact of implementing different types of suturing materials and techniques of vaginal cuff closure in robotic assisted laparoscopic hysterectomy on cost, operative time and post operative surgical outcomes.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Henry Ford Hospital

Detroit, Michigan, 48202, United States

About this study

Robotic assisted laparoscopic surgery is the fastest growing new modality in gynecologic surgery. Surgeons are adapting it to perform both benign and oncologic gynecologic procedures. Therefore, the fastest growing robotic procedure in the united states is hysterectomy.

The literature in laparoscopic hysterectomy, both robotic and non-robotic, reports a complication of vaginal closure disruption after hysterectomy higher than with abdominal surgery. Reasons hypothesized for this phenomenon include colpotomy (vaginal incision) technique, vaginal closure technique, and types of suture. At present, no further follow up studies have been done to test some of these hypothesis. In light of the rapid adoption of this approach to hysterectomy, more data on this issue will help the physician in counseling patients regarding complications, as well as helping surgeons choose materials and techniques in their hysterectomies which will diminish the chance for this unfortunate complication, which causes pain, hospitalization and excess morbidity after the original surgery.

Additionally, a parallel development of newer suturing materials, the so-called "barbed" self-anchoring sutures, typically fabricated from monofilament materials, have been reported used in laparoscopic hysterectomies in case series. The relative contribution of theses newer materials to the rates of cuff disruption is unknown.

The protocol proposes testing the null hypothesis that different suture materials and methods of closure do not cause a significant difference in the rates of vaginal cuff disruption after robotic assisted laparoscopic total hysterectomy.

Study design is a prospective randomized controlled trial. Patients will be blindly randomized to one of the 3 closure techniques using 3 different materials. Technique and material by necessity can not be blinded to the surgeon. Otherwise, standard surgical technique will be used. Followup in 2 and 6 weeks for clinical assessment will be performed. To asses the long term of cuff disruption, a 12 month interview will be also conducted. Data points will include operative time for closure, postoperative pain at 2 and 6 weeks, postoperative pain with urination/voiding at 2 and 6 weeks, spotting, bleeding and /or frank vaginal disruption documented at 2 and 6 weeks, and pain and presence of dyspareunia at 12 months will be assessed.

Cost associated with cuff closure will be calculated by addition of OR time and material cost.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Women scheduled for robotic assisted laparoscopic hysterectomy

Exclusion criteria

  • Patients who will not consent.
  • Hysterectomy due to malignant conditions.

Treatment and study plan

V-lock suture

Device

Vicryl suture

Device

Lapra-Ty II

Device

Primary outcomes

  1. Vaginal cuff dehiscence

    Time frame: 12 months

    Postoperative inspection for vaginal cuff dehiscence

Secondary outcomes

  1. Complications

    Time frame: 6 weeks

    Post-operative vaginal bleeding, bowel or urinary dysfunction

  2. Operative time costs

    Time frame: 1 year

    Measurement of operative time and determination of unit cost per surgery

  3. Suturing material costs

    Time frame: 1 year

    Comparison of the amount and type of suture utilized per surgery

  4. Operative suturing time

    Time frame: During surgery

    Time to complete Vaginal cuff closure

  5. Post operative pain

    Time frame: 6 weeks

    Visual Analog Scale

  6. Vaginal bleeding/ spotting

    Time frame: 12 months

    Presence of postoperative vaginal bleeding

  7. Resumption of sexual activity

    Time frame: 12 months

    Time to resumption of intercourse

  8. Dyspareunia

    Time frame: 12 months

    Assessment of Painful Intercourse

Sponsors and collaborators

Lead sponsor

Henry Ford Health System

Other

Registry information

Important dates

Study start
2010
Primary completion
2016
Study completion
2016
First posted
Mar 2, 2016
Registry last updated
Dec 6, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.