The goal of this clinical trial was to compare two surgical techniques in female patients with full-thickness rectal prolapse. The main questions it aimed to answer were: 1. Does modified rectosacrouteropexy with pelvic peritonization improve postoperative anatomical outcomes compared with conventional Wells rectopexy? 2. Does modified rectosacrouteropexy with pelvic peritonization improve postoperative functional outcomes compared with conventional Wells rectopexy? Researchers compared modified rectosacrouteropexy with pelvic peritonization with conventional Wells rectopexy to assess postoperative recurrence, complications, anorectal manometry, defecography findings, and pelvic floor symptom scores. Participants underwent one of the assigned surgical procedures and were followed after surgery with clinical assessment and pelvic floor function testing.
This is a prospective randomized comparative study conducted at Azerbaijan Medical University. Female patients with full-thickness rectal prolapse are assigned to modified rectosacrouteropexy with pelvic peritonization or conventional Wells rectopexy. Participants are followed for postoperative anatomical and functional outcomes, including recurrence, complications, anorectal manometry findings, defecography findings, and pelvic floor symptom scores.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
36
Surgical treatment for full-thickness rectal prolapse using modified rectosacrouteropexy with pelvic peritonization.
Conventional surgical rectopexy procedure for full-thickness rectal prolapse
Surgery, Biochemistry
Baku, Azerbaijan
Postoperative rectal prolapse recurrence
Recurrence of full-thickness rectal prolapse after surgery, assessed during postoperative follow-up
Time frame: Up to 24 months after surgery
Postoperative complications
Occurrence of postoperative complications, including constipation, fistula formation, and mesh-related complications.
Time frame: Up to 24 months after surgery
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