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CTRI Number  CTRI/2024/10/076101 [Registered on: 30/10/2024] Trial Registered Prospectively
Last Modified On: 04/10/2025
Post Graduate Thesis  No 
Type of Trial  Interventional 
Type of Study   Surgical/Anesthesia 
Study Design  Randomized, Parallel Group Trial 
Public Title of Study   Comparison of two laparoscopic surgeries for pelvic organ prolapse- a randomized controlled trial  
Scientific Title of Study   Laparoscopic Sacropexy Vs Pectopexy for apical prolapse – A single blind randomized controlled trial  
Trial Acronym  NIL 
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  DR MUKTA AGARWAL 
Designation  Professor 
Affiliation  All india institute of medical sciences Patna 
Address  Room 257 Gyne OPD AIIMS Patna Phulwarisharif
Room 257 Gyne OPD AIIMS Patna Phulwarisharif
Patna
BIHAR
801507
India 
Phone  07903342351  
Fax    
Email  dr.sudwita11133@aiimspatna.org  
 
Details of Contact Person
Scientific Query
 
Name  DR MUKTA AGARWAL 
Designation  Professor 
Affiliation  All india institute of medical sciences Patna 
Address  Room 257 Gyne OPD AIIMS Patna Phulwarisharif
Room 257 Gyne OPD AIIMS Patna Phulwarisharif

BIHAR
801507
India 
Phone  07903342351  
Fax    
Email  dr.sudwita11133@aiimspatna.org  
 
Details of Contact Person
Public Query
 
Name  DR MUKTA AGARWAL 
Designation  Professor 
Affiliation  All india institute of medical sciences Patna 
Address  Room 257 Gyne OPD AIIMS Patna Phulwarisharif
Room 257 Gyne OPD AIIMS Patna Phulwarisharif

BIHAR
801507
India 
Phone  07903342351  
Fax    
Email  dr.sudwita11133@aiimspatna.org  
 
Source of Monetary or Material Support  
All India Institute of Medical Sciences Patna Phulwarisharif Patna Bihar-801507 India 
 
Primary Sponsor  
Name  All india institute of medical sciences Patna 
Address  Phulwarisharif Patna Bihar-801507 India 
Type of Sponsor  Government medical college 
 
Details of Secondary Sponsor  
Name  Address 
NIL  NIL 
 
Countries of Recruitment     India  
Sites of Study  
No of Sites = 1  
Name of Principal Investigator  Name of Site  Site Address  Phone/Fax/Email 
Dr Mukta Agarwal  All india institute of medical sciences Patna  Room 257 gyne OPD Department of Obstetrics and Gynaecolgy AIIMS Patna
Patna
BIHAR 
07633071844

dr.sudwita11133@aiimspatna.org 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Institutional Ethics Committee, AIIMS,Patna  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: N993||Prolapse of vaginal vault after hysterectomy,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  Laparoscopic pectopexy  The bilateral ileo-pectineal ligament will be fastened to the vaginal vault (pectopexy) or anterior cervix during this treatment. First, the bladder will be pulled down and the vesico-vaginal fold will be opened . One by one, the peritoneal layer will be opened up towards the pelvic sidewalls to expose the white, sparkling ligament next to the ilio-psoas muscles insertion - the ileo-pectineal ligament, also known as the Cooper ligament. At the base of the triangle, encompassed by the external iliac vein (cranial/ventral), the obturator nerve (dorsal/caudal), and the round ligament, the iliopectineal ligament will be identified. The vaginal apex or anterior then will be prepared for the mesh fixation anteriorly and posteriorly, and the peritoneal layer will be opened towards it on both sides. Using non-absorbable ethibond 2-0 intracorporeal suturing, a polypropylene, monofilament mesh (15 x 15 cm) will be sutured tension-free to the vaginal apex or anterior cervix, and both iliopectineal ligaments using ethibond 2-0 and surgical tacker if needed. Finally, an absorbable 2-0 vicryl suture will be used to cover the peritoneum over the mesh. This surgery will be done only once and the estimated duration of surgery will be 45-90 minutes  
Comparator Agent  Laparoscopic sacropexy  This operation will involve fixing the vaginal vault (sacro-colpopexy) to the sacrums anterior longitudinal ligament (S1-S2). The anterior longitudinal ligament will be exposed when the peritoneum covering the sacral promontory will be split open. Subsequently, the peritoneal incision will be expanded in the direction of Douglas pouch, reaching till vault or cervix, which is situated between the rectum and right ureter. A Y-shaped mesh (15 x 15 cm) covering the cervix or vaults front and posterior walls will be introduced and sewn shut with 2-0 ethibond. After that, the vault will be suspended to the sacral promontory with mesh covered by same suture or with help of surgical tacker followed by peritoneal closure to prevent erosion. This surgery will be done only once and the estimated duration of surgery will be 45-90 minutes 
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  65.00 Year(s)
Gender  Female 
Details  Women with apical prolapse of pelvic organ prolapse-quantification (POP-Q)≥ stage 2  
 
ExclusionCriteria 
Details  1- Women with active pelvic inflammatory disease
2- History of vaginal prolapse corrective surgery
3- Ongoing pregnancy
4- History of premalignant or malignant diseases of uterus, cervix, or adnexa,
5- Any contraindication for laparoscopic surgery
6- Patient unfit for anesthesia
7- Not giving consent to participate in the trial
 
 
Method of Generating Random Sequence   Computer generated randomization 
Method of Concealment   Sequentially numbered, sealed, opaque envelopes 
Blinding/Masking   Participant Blinded 
Primary Outcome  
Outcome  TimePoints 
To compare overall operating time between two methods
 
0 days, 7 days
 
 
Secondary Outcome  
Outcome  TimePoints 
To compare post-operative complications using Clavien- Dindo classification and short-term outcome between two methods
 
0 days, 7 days 
To compare quality of life between two methods using validated questionnaires (PISQ-IR) at 7 days after surgery and then every 6 months upto 2 years post-surgery

 
7 days, 6 months, 12 months, 18 months, 24 months 
To compare recurrence rate within two years between two methods  24 months 
 
Target Sample Size   Total Sample Size="50"
Sample Size from India="50" 
Final Enrollment numbers achieved (Total)= "Applicable only for Completed/Terminated trials"
Final Enrollment numbers achieved (India)="Applicable only for Completed/Terminated trials" 
Phase of Trial   Phase 3/ Phase 4 
Date of First Enrollment (India)   01/12/2024 
Date of Study Completion (India) Applicable only for Completed/Terminated trials 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) Applicable only for Completed/Terminated trials 
Estimated Duration of Trial   Years="3"
Months="0"
Days="0" 
Recruitment Status of Trial (Global)
Modification(s)  
Not Applicable 
Recruitment Status of Trial (India)  Open to Recruitment 
Publication Details   N/A 
Individual Participant Data (IPD) Sharing Statement

Will individual participant data (IPD) be shared publicly (including data dictionaries)?  

Response - NO
Brief Summary  

Summary

 

 

Background: Pelvic organ prolapse (POP) is a common disorder characterized by downward displacement of pelvic organs through vaginal wall. Laparoscopic pectopexy (LP) is a new surgical technique now a days in addition to the conventional laparoscopic sacropexy (LS) in correcting apical prolapse. Sacropexy reduces anatomical recurrence and complication rates, while LP offers shorter operation times and lower complication rates compared to both native tissue repairs and sacropexy.

Rationale: Intraoperative bleeding is more likely with sacropexy since it requires dissection of the presacral area, especially in elderly and patients using anticoagulants. Since the whole pectopexy procedure takes place in the anterior pelvis, patients with substantial adhesions are spared dissection in the deep pelvis.

Novelty: So far very few randomised controlled trials have been conducted comparing lap sacropexy and lap pectopexy. Most published studies are retrospective studies or prospective cohort studies. Moreover, there are hardly any study comparing long term outcome.

Aim: Comparison of intraoperative parameters and post-operative Surgical outcomes and complications between laparoscopic sacropexy and pectopexy

Objectives:

Primary objective

1.     To compare overall operating time between two methods

2.     To compare post-operative complications using Clavien- Dindo classification and short-term outcome between two methods

3.     To compare quality of life between two methods using validated questionnaires (PISQ-IR) at 7 days after surgery and then every 6 months upto 2 years post-surgery

 

Secondary objective

1.     To compare recurrence rate within two years between two methods

Methods: This will be a prospective randomised controlled trial to be conducted at Patna after ethical approval. Total of 50 women fulfilling the inclusion criteria will be screened for the study and their demographic details will be collected. They will be assigned to either laparoscopic sacropexy or pectopexy group in a 1:1 ratio using a random permuted-block algorithm via an interactive Web-based response system. The patient will be blinded to group allocation. A single surgeon will perform all surgeries. Data will be collected using pre-structured data collection proformas. Statistical analysis will be done using appropriate tests of significance. Interim analysis will be done at six months post-surgery.

Expected outcome.

For apical prolapse, laparoscopic pectopexy is anticipated to be a safe, practical, and comfortable alternative to traditional sacropexy. It is anticipated that laparoscopic pectopexy will result in a much shorter mesh fixation time, a shorter operating time, and less blood loss than laparoscopic sacropexy .Comparison of outcomes of these two surgical techniques will help in deciding the best feasible surgery with better outcomes and lesser complications.

 
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