Outcomes on Abdominal Versus Vaginal Morcellation At Time of Hysterectomy

Sponsor
University of Texas Southwestern Medical Center (Other)
Overall Status
Recruiting
CT.gov ID
NCT04434066
Collaborator
(none)
36
1
2
41.7
0.9

Study Details

Study Description

Brief Summary

The purpose of the study is to investigate differences in perioperative and postoperative outcomes between the abdominal (AM) versus vaginal (VM) routes of contained morcellation in participants undergoing laparoscopic total hysterectomies in a randomized controlled trial.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Total Laparoscopic Hysterectomy
N/A

Detailed Description

The purpose of the proposed study is to investigate differences in intraoperative and postoperative outcomes between the abdominal (AM) versus vaginal (VM) routes of contained morcellation in subjects undergoing laparoscopic total hysterectomies in a randomized surgical trial.

Objectives:
  1. To evaluate differences in total operating time between subjects undergoing AM compared to VM.

  2. To evaluate differences in morcellation time between AM and VM.

  3. To evaluate differences in the amount of total narcotic use during hospital admission between AM and VM through morphine milligram equivalents (MME).

  4. To evaluate differences in the patient's subjective pain assessment via Visual Analogue Scale (VAS) before surgery, at 2-weeks, and at 6 week post-operative visits in both AM and VM groups.

  5. To evaluate differences in the patient's pain medication usage as reported by the patient verbally at 24-hours post-operatively and 2-weeks post surgery between AM and VM groups.

  6. To evaluate differences in body image survey (BIS) scores at enrollment and 6-week postoperative visit between the AM group compared to VM group.

  7. To evaluate differences in overall Quality of Life (QoL) scores at enrollment and 6-week postoperative visit between the AM group compared to VM group.

  8. To evaluate differences in Quality of Recovery (QoR) scores at enrollment and at 24-hours post-operatively, and then 2-weeks post surgery between AM and VM group.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
36 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
A Comparison of Perioperative and Patient-Centered Outcomes With Abdominal Versus Vaginal Morcellation: A Randomized-Controlled Trial
Actual Study Start Date :
Jan 8, 2020
Anticipated Primary Completion Date :
Jun 30, 2023
Anticipated Study Completion Date :
Jun 30, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Abdominal Morcellation

Abdominal morcellation will occur following completion of the hysterectomy. Route of incision will be either suprapubic or umbilical incision - based on surgeon preferences. All steps and instruments have been standardized for abdominal morcellation.

Procedure: Total Laparoscopic Hysterectomy
Participants will be randomized into either abdominal or vaginal morcellation at time of total laparoscopic hysterectomy

Experimental: Vaginal Morcellation

Vaginal morcellation will occur following completion of the hysterectomy. All steps and instruments have been standardized for vaginal morcellation.

Procedure: Total Laparoscopic Hysterectomy
Participants will be randomized into either abdominal or vaginal morcellation at time of total laparoscopic hysterectomy

Outcome Measures

Primary Outcome Measures

  1. Mean difference in total operating room time [intraoperative]

    Total operating room time is defined as skin incision to skin closure

Secondary Outcome Measures

  1. Mean difference from baseline in Body Image Scale Score to 6-weeks post-operatively [through study completion up to 6-weeks post-operatively]

    Body Image Scale will be collected at baseline, and 6-weeks post-operatively. Body Image Scale will be scored from 10 to 40 points maximum, with higher scores referring to being "very dissatisfied" with overall body image

  2. Mean difference from baseline in Pain Visual Analogue Scale to 6-weeks post-operatively [through study completion up to 6-weeks post-operatively]

    Pain Visual Analogue Scale will be collected at baseline, and 6-weeks post-operatively. VAS scale will be measured from 0 to 10mm, with higher scores referring to more pain experienced

  3. Mean difference from baseline in Quality of Recovery Score to 2-weeks post-operatively [through study completion up to 6-weeks post-operatively]

    Quality of Recovery will be collected at baseline, 24-hours, and 2-weeks post-operatively. Quality of Recovery will be scored from 10 to 100, with higher scores referring to better quality of recovery

  4. Mean difference from baseline in Quality of Life Score to 6-weeks post-operatively [through study completion up to 6-weeks post-operatively]

    Quality of Life Scores will be collected at baseline, and 6-weeks post-operatively. The Quality of Life Score will be scored from 11 to 44, with higher scores referring to better quality of life

  5. Morcellation Time [intraoperative]

    Defined as specimen bag introduction to specimen bag removal

  6. Rates of Post-Operative Complications [through study completion up to 6-weeks post-operatively]

    Post-operative complications will be collected including: readmission to the hospital or emergency room, number of visits seen in the clinic, diagnoses of infection, bleeding, blood transfusions, surgery-related injuries, reoperations, and overall mortality

  7. Mean difference in the dosages of morphine milligram equivalent (MME) for post-operative pain between abdominal and vaginal morcellation [after surgery to 2-weeks post-operatively]

    The type and dosages of various narcotics will be recorded between both groups following surgery until 2-weeks post-operatively

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 50 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • All benign total laparoscopic hysterectomy and/or robotic-assisted hysterectomy, +/- unilateral salpingo-oophorectomy or bilateral salpingo-oophorectomy

  • Adnexectomy, cystectomy, tubal procedures at time of hysterectomy

  • Age >18 years old

  • Uterus >12 weeks, or >250 grams (based on imaging), or requiring morcellation based on clinical judgment at time of pre-operative enrollment

  • English and Spanish speaking

Exclusion Criteria:
  • Pre-malignant conditions (i.e. endometrial intraepithelial neoplasia, high-grade cervical intraepithelial neoplasia), known gynecologic malignancy, and any contraindications to abdominal or vaginal morcellation

  • Planned concurrent procedures (i.e. hernia repair, bowel resections, anti-incontinence procedures, prolapse repair, and mastectomy)

  • Appendectomy for endometriosis is not excluded

  • No chronic pain disorders requiring medical management (endometriosis can be included)

  • Planned abdominal hysterectomy or vaginal hysterectomy candidates

  • Conversion to laparotomy or inability to complete morcellation

  • Contraindications to laparoscopy

Contacts and Locations

Locations

Site City State Country Postal Code
1 UT Southwestern Medical Center Dallas Texas United States 75229

Sponsors and Collaborators

  • University of Texas Southwestern Medical Center

Investigators

  • Principal Investigator: Kimberly A Kho, MD, UT Southwestern Medical Center

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Kimberly Kho, Associate Professor, University of Texas Southwestern Medical Center
ClinicalTrials.gov Identifier:
NCT04434066
Other Study ID Numbers:
  • STU-2019-1402
First Posted:
Jun 16, 2020
Last Update Posted:
Jul 29, 2022
Last Verified:
Jul 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Kimberly Kho, Associate Professor, University of Texas Southwestern Medical Center
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 29, 2022