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Abdominal Pectopexy Versus Abdominal Sacral Hysteropexy.

Primary Purpose

Genital Prolapse

Status
Completed
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
Abdominal Pectopexy
Abdominal Sacral Hysteropexy
Sponsored by
Ain Shams University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Genital Prolapse

Eligibility Criteria

20 Years - 40 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Women with stage 2 to 4 uterine prolapse.
  • BMI from ≤ 35 kg\m2.
  • Women of any parity including nulliparas will be included.
  • Age of female patients ranges from 20 to 40 years.

Exclusion Criteria:

  • Previous correction of apical prolapse.
  • Inoperable co-existing uterine pathology

Sites / Locations

  • Faculty of medicine, Ain Shams University

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

study group

Arm Description

Women with stage 2 to 4 uterine prolapse. BMI from ≤ 35 kg\m2. Women of any parity including nulliparas will be included. Age of female patients ranges from 20 to 40 years.

Outcomes

Primary Outcome Measures

Efficacy, After the procedure there will be follow up visits at 3 months to detect the efficacy of the procedure by using POP-Q system.
The POP-Q system is a technique that measures compartment prolapse relative to the anatomic landmark of the hymen.Prolapse points proximal to the hymen are given a negative value, whereas positive values are given to points that protrude past the hymen. 6 points are delineated, including two on the anterior vaginal wall (Aa, Ba), two on the vaginal apex (C, D), and two on the posterior vaginal wall (Ap, Bp). Points Gh, Pb, and TVL describe the genital hiatus, perineal body, and total vaginal length, respectively. Stage 0: no demonstrable prolapse Stage 1: the most distal portion of the prolapsed segment is >1 cm above the level of the hymen Stage 2: the most distal portion of the prolapsed segment is >1 cm or less proximal or distal to the hymen Stage 3: the most distal portion of the prolapsed segment protrudes >1 cm below the hymen but 2 cm less than the total length of the vagina Stage 4: complete eversion of the vagina

Secondary Outcome Measures

Operative time
Total operative time from skin incision till closure of the skin and excluding time of concomitant surgical procedures.
Intra operative blood loss
Intra operative blood loss will be estimated via: Amount of blood in suction bottle. Drop in postoperative hemoglobin and hematocrit when compared with preoperative values
Intra operative complications
Intra operative complications including: Need for blood transfusion. Bowel or bladder injury.
Post operative complications
Subfascial hematoma or pelvic hematoma. Surgical site infection. Urinary tract infection. Need for post-operative blood transfusion. Postoperative bowel or urinary tract complications
Post operative pain
Postoperative pain will be assessed using the linear 10cm visual analogue scale. Range is from 10(unbearable pain) to zero (no pain).

Full Information

First Posted
April 13, 2021
Last Updated
April 21, 2021
Sponsor
Ain Shams University
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1. Study Identification

Unique Protocol Identification Number
NCT04856709
Brief Title
Abdominal Pectopexy Versus Abdominal Sacral Hysteropexy.
Official Title
Abdominal Pectopexy Versus Abdominal Sacral Hysteropexy as Conservative Surgeries for Genital Prolapse: A Randomized Control Trial
Study Type
Interventional

2. Study Status

Record Verification Date
April 2021
Overall Recruitment Status
Completed
Study Start Date
June 1, 2019 (Actual)
Primary Completion Date
June 1, 2020 (Actual)
Study Completion Date
April 1, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Ain Shams University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
This study aims to compare between abdominal pectopexy and abdominal sacral hysteropexy in terms of efficacy (assessed by POP-Q system), intra and postoperative complications.
Detailed Description
Pelvic organ prolapse (POP), the herniation of the pelvic organs to or beyond the vaginal walls, is a common condition. Many women with prolapse experience symptoms that impact daily activities, sexual function, and exercise. The presence of POP can have a detrimental impact on body image and sexuality (Lowder et al., 2011). Nulliparous prolapse is reported to account for 1.5% to 2% of all cases of genital prolapse (Virkud, 2016). The incidence rises to 5 -8 % for young women who have delivered one or two children. As this type of prolapse occurs at a younger age, the surgical technique should not only reduce the prolapse but also retain the reproductive function. Various conservative surgeries have been described in the past, each having their own merits and de-merits (Rameshkumar et al., 2017). Pelvic organ prolapse (POP) is affecting women of all ages. Epidemiological studies suggest a lifetime risk of prolapse or incontinence surgery of between 7 and 19% (Olsen et al., 1997; Smith et al., 2010). In an ageing population, the incidence of these surgeries would only be expected to increase, although the increasing Caesarean Section rates and smaller family size in recent years will have a negative impact on the prevalence of these conditions. There are many approaches to the surgical correction of POP, which frequently reflect the nature and anatomical site of the defective support, but essentially the surgeon has to decide whether to perform this surgery vaginally or via the abdomen as an open or laparoscopic procedure. If performed vaginally, further decisions regarding the use of synthetic or biological graft to reinforce the repair need to be made (Cvach and Dwyer, 2012). Pectopexy is a new technique for apical repair in which lateral parts of the iliopectineal ligament are used for cuff or cervix suspension. This new method is considered a simple, safe procedure, especially in patients whose surgical exploration is difficult (Banerjee and Noé, 2011). This method uses the iliopectineal ligament on both sides for the mesh fixation, (Banerjee and Noé, 2011). so there is no restriction caused by the mesh. The mesh follows natural structures (round and broad ligaments) without crossing sensitive spots, such as the ureter or bowel. The hypogastric trunk is at a safe distance and out of danger. The iliopectineal ligament is an extension of the lacunar ligament that runs on the pectineal line of the pubic bone (Faure et al., 2001), and is significantly stronger than the sacrospinous ligament and the arcus tendineus of the pelvic fascia (Cosson et al., 2003). The structure is strong, and holds suture well Abdominal sacral hysteropexy remains a viable alternative for women undergoing pelvic reconstructive surgery who wish to retain their uteri, providing comparable rates of overall improvement and symptom change. Avoiding hysterectomy decreases the risk of mesh erosion but may increase the risk of subsequent recurrent prolapse, specifically in the anterior compartment (Cvach and Cundiff, 2008). Although sacrocolpopexy has been the most effective option over time, the procedure is still associated with some problems, and the most frequently reported complications include defecation disorders and stress urinary incontinence (SUI)

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Genital Prolapse

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Study design: Randomized Controlled clinical Trial Study Setting: Ain Shams maternity hospital. Study Population: The study included 80 women divided into 2 groups: Group A: 40 women underwent abdominal pectopexy. Group B: 40 women underwent abdominal sacral hysteropexy.
Masking
None (Open Label)
Allocation
N/A
Enrollment
80 (Actual)

8. Arms, Groups, and Interventions

Arm Title
study group
Arm Type
Other
Arm Description
Women with stage 2 to 4 uterine prolapse. BMI from ≤ 35 kg\m2. Women of any parity including nulliparas will be included. Age of female patients ranges from 20 to 40 years.
Intervention Type
Procedure
Intervention Name(s)
Abdominal Pectopexy
Intervention Description
Pectopexy is a new technique for apical repair in which lateral parts of the iliopectineal ligament are used for cuff or cervix suspension.
Intervention Type
Procedure
Intervention Name(s)
Abdominal Sacral Hysteropexy
Intervention Description
Abdominal sacrocolpopexy is a procedure that uses a mesh material to support the top of the vagina to treat pelvic prolapse.
Primary Outcome Measure Information:
Title
Efficacy, After the procedure there will be follow up visits at 3 months to detect the efficacy of the procedure by using POP-Q system.
Description
The POP-Q system is a technique that measures compartment prolapse relative to the anatomic landmark of the hymen.Prolapse points proximal to the hymen are given a negative value, whereas positive values are given to points that protrude past the hymen. 6 points are delineated, including two on the anterior vaginal wall (Aa, Ba), two on the vaginal apex (C, D), and two on the posterior vaginal wall (Ap, Bp). Points Gh, Pb, and TVL describe the genital hiatus, perineal body, and total vaginal length, respectively. Stage 0: no demonstrable prolapse Stage 1: the most distal portion of the prolapsed segment is >1 cm above the level of the hymen Stage 2: the most distal portion of the prolapsed segment is >1 cm or less proximal or distal to the hymen Stage 3: the most distal portion of the prolapsed segment protrudes >1 cm below the hymen but 2 cm less than the total length of the vagina Stage 4: complete eversion of the vagina
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Operative time
Description
Total operative time from skin incision till closure of the skin and excluding time of concomitant surgical procedures.
Time Frame
60- 240 minutes
Title
Intra operative blood loss
Description
Intra operative blood loss will be estimated via: Amount of blood in suction bottle. Drop in postoperative hemoglobin and hematocrit when compared with preoperative values
Time Frame
60- 240 minutes
Title
Intra operative complications
Description
Intra operative complications including: Need for blood transfusion. Bowel or bladder injury.
Time Frame
60- 240 minutes
Title
Post operative complications
Description
Subfascial hematoma or pelvic hematoma. Surgical site infection. Urinary tract infection. Need for post-operative blood transfusion. Postoperative bowel or urinary tract complications
Time Frame
1 week
Title
Post operative pain
Description
Postoperative pain will be assessed using the linear 10cm visual analogue scale. Range is from 10(unbearable pain) to zero (no pain).
Time Frame
after 6 hours, 12 hours and 24 hours from the operation

10. Eligibility

Sex
Female
Gender Based
Yes
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Women with stage 2 to 4 uterine prolapse. BMI from ≤ 35 kg\m2. Women of any parity including nulliparas will be included. Age of female patients ranges from 20 to 40 years. Exclusion Criteria: Previous correction of apical prolapse. Inoperable co-existing uterine pathology
Facility Information:
Facility Name
Faculty of medicine, Ain Shams University
City
Cairo
ZIP/Postal Code
11591
Country
Egypt

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Time Frame
6 months after publication

Learn more about this trial

Abdominal Pectopexy Versus Abdominal Sacral Hysteropexy.

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