Department of Ob & Gyn, Peking Union Medical College Hospital
Beijing, Beijing Municipality, 100730, China
NCT Number: NCT03005613
A Prospective, Randomized Comparison of Efficacy and Effect on Quality of Life Between Sacrospinous Ligament Fixation and Ischial Spine Fascia Fixation.
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Notify Me25 year–65 year
Female
Interventional
Not applicable
Beijing, Beijing Municipality, 100730, China
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:
Sample size:76 patients (38 in ISFF group, 38 in SSLF group)
Primary endpoint:
•objective success rates at 3 months after operations.
Secondary endpoints:
Safety endpoints: complications
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The participants will receive ischial spine fascia fixation.
The participants will receive sacrospinous ligament fixation.
Time frame: 3 months after operation
no prolapse, stage I or only asymptomatic stage II prolapse
Time frame: Change from Baseline in PFDI-20 at 3 months and 1 year
to evaluate the quality of life in 3 domains
Time frame: Change from Baseline in PFIQ-7 at 3 months and 1 year
to evaluate the quality of life in 3 domains
Time frame: Change from Baseline in PISQ-12 at 3 months and 1 year
to evaluate the sexual function
Time frame: through study completion, an average of 1 year
peri-operative:massive bleeding, organ injury; post-operative: pelvic hematoma, pain, de novo UI, de novo dyspareunia
Time frame: 3 months after operation
more than asymptomatic stage II prolapse after 3 months
Time frame: 1 year after operation
Patient's response as improved or greatly improved
Peking Union Medical College Hospital
Other
A Prospective, Randomized Comparison of Efficacy and Effect on Quality of Life Between Sacrospinous Ligament Fixation and Ischial Spine Fascia Fixation
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.
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