Total Versus Subtotal Abdominal Hysterectomy at Time of Abdominal Sacrocolpopexy
Primary Purpose
Prolapse Genital
Status
Completed
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
total abdominal hysterectomy
Subtotal abdominal hysterectomy
Sponsored by
About this trial
This is an interventional prevention trial for Prolapse Genital focused on measuring hysterectomy, sacrocolpopexy
Eligibility Criteria
Inclusion Criteria:
- nonhystrectomized patients who will undergo sacrocolpopexy for uterovaginal prolapse
Exclusion Criteria:
- women age less than 40
- desire to retain the uterus
- women who are unfit for lengthy surgery
Sites / Locations
- South Valley University, Qena Faculty of Medicine, Obstetrics and Gynecology Department
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
total abdominal hysterectomy
subtotal abdominal hysterectomy
Arm Description
Total abdominal hysterectomy at the time of sacrocolpopexy operation for uterovaginal prolapse
subtotal abdominal hysterectomy at the time of sacrocolpopexy operation for uterovaginal prolapse
Outcomes
Primary Outcome Measures
Mesh erosion
Mesh exposure through the lumen of the vagina, bladder, or rectum
Secondary Outcome Measures
recurrence
recurrence of vaginal wall prolapse or vault prolapse
Full Information
NCT ID
NCT04178473
First Posted
November 24, 2019
Last Updated
September 20, 2021
Sponsor
South Valley University
1. Study Identification
Unique Protocol Identification Number
NCT04178473
Brief Title
Total Versus Subtotal Abdominal Hysterectomy at Time of Abdominal Sacrocolpopexy
Official Title
Total Versus Subtotal Abdominal Hysterectomy at Time of Abdominal Sacrocolpopexy
Study Type
Interventional
2. Study Status
Record Verification Date
September 2021
Overall Recruitment Status
Completed
Study Start Date
January 1, 2019 (Actual)
Primary Completion Date
January 30, 2021 (Actual)
Study Completion Date
May 30, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
South Valley University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Uterovaginal prolapse is a common disease. Due to high failure rate that occur following vaginal hysterectomy, sacrocolpopexy is investigated by many resarchers to manage uterovaginal prolapse in non-hystrectomized women.
In this study the investigator will compare the result of total versus subtotal hysterectomy at the time of sacrocolpopexy.
Study design: Randomized controlled trial
Intervention:
Group A will have total abdominal hysterectomy Group B will have subtotal abdominal hysterectomy
Detailed Description
Uterovaginal prolapse is a common disease. Sacrocolpopexy is essentially invented to manage prolapse of the vault following hysterectomy. Due to high failure rate that occur following vaginal hysterectomy, sacrocolpopexy is investigated by many resarchers to manage uterovaginal prolapse in non-hystrectomized women. The main drawback of sacrocolpopexy is the risk of mesh erosion. The incidence of mesh erosion is 0-5% at follow up of 1 year and 0.5% at follow up of 7 years. After total hysterectomy, the mesh is sutured to the vaginal wall using non-absorbable sutures. Sutures that span the whole thickness of vaginal and involve the vaginal skin was considered the probable factor that result in mesh erosion. After subtotal hysterectomy, the mesh is fixed to the anterior and the posterior cervical surfaces. The cervix has thick wall and the risk associated with "deep" stiches does not exist.
In this study the investigator will compare the result of total versus subtotal hysterectomy at the time of sacrocolpopexy.
Patients and methods
Study design:
Randomized controlled trial
Patients:
Data will be collected from the patients admitted to the obstetrics and gynecology department, Qen faculty of medicine, South Valley University, Egypt from the 1st of January 2019 until 30th of December 2019. Follow up data will be collected until 30th of December 2020. Written consent will be obtained at time of recruitment. The Inclusion criteria are nonhystrectomized patients who will undergo sacrocolpopexy. Exclusion criteria were (1) women age less than 40; (2) desire to retain the uterus; (3) women who are unfit for lengthy surgery. Randomization will be through closed envelop method.
Intervention Group A will have total abdominal hysterectomy Group B will have subtotal abdominal hysterectomy Sacrocolpopexy will be done using Polypropylene mesh. Both groups will be done by the same surgeon using the following technique: dissection of the vesicovaginal and the rectovaginal spaces to prepare for the site of mesh placement. Dissection will be continued in the rectovaginal septum using sharp and blunt dissection until reaching the level of the levator ani (the length of the posterior vaginal mesh arm is nearly equal to the total vaginal length). The limit of the dissection in the vesicovaginal plane is down to the bladder neck (known by palpation of the Foley's catheter balloon) after lateralization of the ureters. The mesh is sutured to the anterior and the posterior vaginal wall the mesh using non-absorbable sutures. In women with subtotal hysterectomy, the mesh will be also sutured to the cervix. The mesh is then sutured to the anterior longitudinal ligament on the anterior surface of the fifth lumbar vertebra and the sacral promontory using non-absorbable sutures. Suturing of the peritoneum over the mesh will be done.
Outcomes:
The primary outcome will be mesh erosion. Secondary outcomes will be complications including recurrence
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prolapse Genital
Keywords
hysterectomy, sacrocolpopexy
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Group A will have total abdominal hysterectomy Group B will have subtotal abdominal hysterectomy Sacrocolpopexy will be done using Polypropylene mesh for all women with uterovaginal prolapse
Masking
ParticipantCare ProviderInvestigator
Masking Description
Double (Participant, Investigator) closed envelop will be used for randomization. The patient and the investigator will be blinded.
Allocation
Randomized
Enrollment
70 (Actual)
8. Arms, Groups, and Interventions
Arm Title
total abdominal hysterectomy
Arm Type
Active Comparator
Arm Description
Total abdominal hysterectomy at the time of sacrocolpopexy operation for uterovaginal prolapse
Arm Title
subtotal abdominal hysterectomy
Arm Type
Active Comparator
Arm Description
subtotal abdominal hysterectomy at the time of sacrocolpopexy operation for uterovaginal prolapse
Intervention Type
Procedure
Intervention Name(s)
total abdominal hysterectomy
Intervention Description
total abdominal hysterectomy at time of sacrocolpopexy
Intervention Type
Procedure
Intervention Name(s)
Subtotal abdominal hysterectomy
Intervention Description
Subtotal abdominal hysterectomy at time of sacrocolpopexy
Primary Outcome Measure Information:
Title
Mesh erosion
Description
Mesh exposure through the lumen of the vagina, bladder, or rectum
Time Frame
12 months or more
Secondary Outcome Measure Information:
Title
recurrence
Description
recurrence of vaginal wall prolapse or vault prolapse
Time Frame
12 months or more
10. Eligibility
Sex
Female
Gender Based
Yes
Gender Eligibility Description
nonhystrectomized patients who will undergo sacrocolpopexy for uterovaginal prolapse
Minimum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
nonhystrectomized patients who will undergo sacrocolpopexy for uterovaginal prolapse
Exclusion Criteria:
women age less than 40
desire to retain the uterus
women who are unfit for lengthy surgery
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mohammad AM Ahmed, MD
Organizational Affiliation
South Valley University, Qena Faculty of Medicine, Obstetrics and Gynecology Department, Qena, Qena, Egypt
Official's Role
Principal Investigator
Facility Information:
Facility Name
South Valley University, Qena Faculty of Medicine, Obstetrics and Gynecology Department
City
Qinā
State/Province
Qena
Country
Egypt
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
IPD will be shared in unanonomous manner with the predetermined group of researchers
IPD Sharing Time Frame
throughout the period of research until end of the study
IPD Sharing Access Criteria
IPD will be shared with the predetermined group of researchers as accepted by the local ethical and research committee.
Citations:
PubMed Identifier
11005477
Citation
Barrington JW, Edwards G. Posthysterectomy vault prolapse. Int Urogynecol J Pelvic Floor Dysfunct. 2000;11(4):241-5. doi: 10.1007/s001920070033.
Results Reference
background
PubMed Identifier
27595628
Citation
Cayrac M, Warembourg S, Le Normand L, Fatton B. [Does hysterectomy modifies the anatomical and functional outcomes of prolapse surgery?: Clinical Practice Guidelines]. Prog Urol. 2016 Jul;26 Suppl 1:S73-88. doi: 10.1016/S1166-7087(16)30430-4. French.
Results Reference
background
PubMed Identifier
29038834
Citation
Coolen AWM, Bui BN, Dietz V, Wang R, van Montfoort APA, Mol BWJ, Roovers JWR, Bongers MY. The treatment of post-hysterectomy vaginal vault prolapse: a systematic review and meta-analysis. Int Urogynecol J. 2017 Dec;28(12):1767-1783. doi: 10.1007/s00192-017-3493-2. Epub 2017 Oct 16.
Results Reference
background
PubMed Identifier
18976976
Citation
Cundiff GW, Varner E, Visco AG, Zyczynski HM, Nager CW, Norton PA, Schaffer J, Brown MB, Brubaker L; Pelvic Floor Disorders Network. Risk factors for mesh/suture erosion following sacral colpopexy. Am J Obstet Gynecol. 2008 Dec;199(6):688.e1-5. doi: 10.1016/j.ajog.2008.07.029. Epub 2008 Oct 31.
Results Reference
background
PubMed Identifier
27379891
Citation
Ismail S, Duckett J, Rizk D, Sorinola O, Kammerer-Doak D, Contreras-Ortiz O, Al-Mandeel H, Svabik K, Parekh M, Phillips C. Recurrent pelvic organ prolapse: International Urogynecological Association Research and Development Committee opinion. Int Urogynecol J. 2016 Nov;27(11):1619-1632. doi: 10.1007/s00192-016-3076-7. Epub 2016 Jul 5.
Results Reference
background
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Total Versus Subtotal Abdominal Hysterectomy at Time of Abdominal Sacrocolpopexy
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