| 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
|
|
|
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
|
|
|
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. |