Sacrospinous Ligament Fixation vs Ischial Spine Fascia Fixation
Primary Purpose
Urogenital Prolapse
Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
ischial spine fascia fixation
sacrospinous ligament fixation
Sponsored by
About this trial
This is an interventional treatment trial for Urogenital Prolapse focused on measuring Pelvic organ prolapse, Sacrospinous ligament fixation, Ischial spine fascia fixation, Clinical outcome
Eligibility Criteria
Inclusion Criteria:
- age≤65 years, for those scheduled to receive hysterectomy age≥40 years
- patients with symptomatic stage II~IV uterine or vaginal vault prolapse
- receiving SSLF or ISFF in the gynecological department at Peking Union Medical College Hospital
Exclusion Criteria:
- plans to live abroad within follow-up span
- contradiction to these two operations: acute genital infection, narrow vagina (less than two finger-breadth), too-ill to receive operations
- patients with hip joint problem who could not pose a lithotomy position
Sites / Locations
- Department of Ob & Gyn, Peking Union Medical College HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
sacrospinous ligament fixation group
ischial spine fascia fixation group
Arm Description
The patients will receive sacrospinous ligament fixation operation.
The patients will receive ischial spine fascia fixation operation.
Outcomes
Primary Outcome Measures
objective success
no prolapse, stage I or only asymptomatic stage II prolapse
Secondary Outcome Measures
Pelvic Floor Distress Inventory-20 (PFDI-20)
to evaluate the quality of life in 3 domains
Pelvic Floor Impact Questionnaire-7 (PFIQ-7)
to evaluate the quality of life in 3 domains
Pelvic Organ Prolapse/Urinary Incontinence Sexual Questionnaire-12 (PISQ-12)
to evaluate the sexual function
complications
peri-operative:massive bleeding, organ injury; post-operative: pelvic hematoma, pain, de novo UI, de novo dyspareunia
recurrence rate
more than asymptomatic stage II prolapse after 3 months
subjective satisfaction ( according to a scale of 5 degrees: significantly worse, worse, no change, improved, greatly improved)
Patient's response as improved or greatly improved
Full Information
NCT ID
NCT03005613
First Posted
December 15, 2016
Last Updated
December 26, 2019
Sponsor
Peking Union Medical College Hospital
1. Study Identification
Unique Protocol Identification Number
NCT03005613
Brief Title
Sacrospinous Ligament Fixation vs Ischial Spine Fascia Fixation
Official Title
A Prospective, Randomized Comparison of Efficacy and Effect on Quality of Life Between Sacrospinous Ligament Fixation and Ischial Spine Fascia Fixation
Study Type
Interventional
2. Study Status
Record Verification Date
December 2019
Overall Recruitment Status
Unknown status
Study Start Date
January 2017 (Actual)
Primary Completion Date
December 2020 (Anticipated)
Study Completion Date
December 2020 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Peking Union Medical College Hospital
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
A Prospective, Randomized Comparison of Efficacy and Effect on Quality of Life Between Sacrospinous Ligament Fixation and Ischial Spine Fascia Fixation.
Detailed Description
Investigational intervention:SSLF or ISFF operations
Study title:A Prospective, Randomized Comparison of Efficacy and Effect on Quality of Life Between Sacrospinous Ligament Fixation and Ischial Spine Fascia Fixation.
Principal Investigator:Chang Ren, M.D., Department of Obstetrics & Gynecology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College.
Study subjects:Adult patients with symptomatic stage II~IV pelvic organ prolapse will be eligible if all the inclusion criteria are met and without any reason for exclusion.
Study objectives:The primary objective of this study is to assess the short and mid-term efficacy of Sacrospinous Ligament Fixation and Ischial Spine Fascia Fixation in treating stage II~ IV pelvic organ prolapse and their recurrence rate as well as their impacts on quality of life.
Study design:Prospective, Single-Blind, Randomized, Clinical Trial
Intervention:
ISFF group:Patients receive ISFF according to randomization.
SSLF group:Patients receive SSLF according to randomization
Sample size:76 patients (38 in ISFF group, 38 in SSLF group)
Primary endpoint:
•objective success rates at 3 months after operations.
Secondary endpoints:
peri-operative parameters .
subjective satisfactory rates at 1 year after operations
quality of life questionnaires at 1 year after operations
Safety endpoints: complications
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Urogenital Prolapse
Keywords
Pelvic organ prolapse, Sacrospinous ligament fixation, Ischial spine fascia fixation, Clinical outcome
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
76 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
sacrospinous ligament fixation group
Arm Type
Active Comparator
Arm Description
The patients will receive sacrospinous ligament fixation operation.
Arm Title
ischial spine fascia fixation group
Arm Type
Experimental
Arm Description
The patients will receive ischial spine fascia fixation operation.
Intervention Type
Procedure
Intervention Name(s)
ischial spine fascia fixation
Intervention Description
The participants will receive ischial spine fascia fixation.
Intervention Type
Procedure
Intervention Name(s)
sacrospinous ligament fixation
Intervention Description
The participants will receive sacrospinous ligament fixation.
Primary Outcome Measure Information:
Title
objective success
Description
no prolapse, stage I or only asymptomatic stage II prolapse
Time Frame
3 months after operation
Secondary Outcome Measure Information:
Title
Pelvic Floor Distress Inventory-20 (PFDI-20)
Description
to evaluate the quality of life in 3 domains
Time Frame
Change from Baseline in PFDI-20 at 3 months and 1 year
Title
Pelvic Floor Impact Questionnaire-7 (PFIQ-7)
Description
to evaluate the quality of life in 3 domains
Time Frame
Change from Baseline in PFIQ-7 at 3 months and 1 year
Title
Pelvic Organ Prolapse/Urinary Incontinence Sexual Questionnaire-12 (PISQ-12)
Description
to evaluate the sexual function
Time Frame
Change from Baseline in PISQ-12 at 3 months and 1 year
Title
complications
Description
peri-operative:massive bleeding, organ injury; post-operative: pelvic hematoma, pain, de novo UI, de novo dyspareunia
Time Frame
through study completion, an average of 1 year
Title
recurrence rate
Description
more than asymptomatic stage II prolapse after 3 months
Time Frame
3 months after operation
Title
subjective satisfaction ( according to a scale of 5 degrees: significantly worse, worse, no change, improved, greatly improved)
Description
Patient's response as improved or greatly improved
Time Frame
1 year after operation
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
25 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
age≤65 years, for those scheduled to receive hysterectomy age≥40 years
patients with symptomatic stage II~IV uterine or vaginal vault prolapse
receiving SSLF or ISFF in the gynecological department at Peking Union Medical College Hospital
Exclusion Criteria:
plans to live abroad within follow-up span
contradiction to these two operations: acute genital infection, narrow vagina (less than two finger-breadth), too-ill to receive operations
patients with hip joint problem who could not pose a lithotomy position
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Chang Ren, M.D.
Phone
+86-134-886-988-61
Email
renchang@pumch.cn
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Chang Ren, M.D.
Organizational Affiliation
Peking Union Medical College Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Ob & Gyn, Peking Union Medical College Hospital
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100730
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Chang Ren, M.D.
Phone
0086-10-69156238
Email
renchang@pumch.cn
First Name & Middle Initial & Last Name & Degree
Chang Ren
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
3342213
Citation
Dwyer PL, Lee ET, Hay DM. Obesity and urinary incontinence in women. Br J Obstet Gynaecol. 1988 Jan;95(1):91-6. doi: 10.1111/j.1471-0528.1988.tb06486.x.
Results Reference
background
PubMed Identifier
9052607
Citation
Sze EH, Karram MM. Transvaginal repair of vault prolapse: a review. Obstet Gynecol. 1997 Mar;89(3):466-75. doi: 10.1016/S0029-7844(96)00337-7.
Results Reference
background
PubMed Identifier
9083302
Citation
Olsen AL, Smith VJ, Bergstrom JO, Colling JC, Clark AL. Epidemiology of surgically managed pelvic organ prolapse and urinary incontinence. Obstet Gynecol. 1997 Apr;89(4):501-6. doi: 10.1016/S0029-7844(97)00058-6.
Results Reference
background
PubMed Identifier
20966694
Citation
Smith FJ, Holman CD, Moorin RE, Tsokos N. Lifetime risk of undergoing surgery for pelvic organ prolapse. Obstet Gynecol. 2010 Nov;116(5):1096-100. doi: 10.1097/AOG.0b013e3181f73729.
Results Reference
background
PubMed Identifier
12548203
Citation
Boyles SH, Weber AM, Meyn L. Procedures for pelvic organ prolapse in the United States, 1979-1997. Am J Obstet Gynecol. 2003 Jan;188(1):108-15. doi: 10.1067/mob.2003.101.
Results Reference
background
PubMed Identifier
24142057
Citation
Barber MD, Maher C. Apical prolapse. Int Urogynecol J. 2013 Nov;24(11):1815-33. doi: 10.1007/s00192-013-2172-1.
Results Reference
background
PubMed Identifier
20223444
Citation
Jones KA, Shepherd JP, Oliphant SS, Wang L, Bunker CH, Lowder JL. Trends in inpatient prolapse procedures in the United States, 1979-2006. Am J Obstet Gynecol. 2010 May;202(5):501.e1-7. doi: 10.1016/j.ajog.2010.01.017. Epub 2010 Mar 11.
Results Reference
background
PubMed Identifier
21060988
Citation
Zhu L, Lang J, Zhang Q. Clinical study of ischia spinous fascia fixation--a new pelvic reconstructive surgery. Int Urogynecol J. 2011 Apr;22(4):499-503. doi: 10.1007/s00192-010-1307-x.
Results Reference
background
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Sacrospinous Ligament Fixation vs Ischial Spine Fascia Fixation
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