Pelvic Organ Prolapse Clinical Trial
Official title:
A Prospective,Multicenter Pilot Study to Evaluate the Clinical Performance of the Ischia Spinous Fascia Fixation Surgery for Pelvic Organ Prolapse.
Pelvic organ prolapse is a common problem. The primary treatment is surgery. Ischia spinous
fascia fixation procedure is developed in China for vaginal apex fixation with native
tissue.
This study is designed to determine the effectiveness and safety of ischia spinous fascia
fixation procedure for the treatment of pelvic organ prolapse stage III.
Patients enrolled into the study will be followed up for up to 3 years after surgery.
Evaluation will take place during surgery and postoperative visit. Stage of prolapse before
and after surgery, patient satisfaction through quality of life and sexual function
questionnaires before and after surgery, and peri-operative complication rates will be
evaluated.
Pelvic Organ prolapse (a feeling of bulge in the vagina) may cause some distressing symptoms
such as loss of control of the bowel or bladder, and may also cause problems with patient's
sex life. An ideal procedure for vaginal apical support should provide a durable suspension,
have minimal complications, and not affect sexual or visceral function.
Ischia spinous fascia fixation procedure is developed in China. It is a transvaginal
procedure used for restoring the vaginal apex support with native tissue. Clinical practice
showed that it was safe, efficient and cost-effective. Recurrent rate after 1 year follow-up
was about 10%, and quality of life improved significantly from the baseline.
The purpose of this multicenter, prospective study is to evaluate the effectiveness and
safety of this procedure in the treatment of symptomatic pelvic organ prolapse.
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Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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