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Completed

NCT Number: NCT06117670

Gamma-irradiated Amniotic Membrane Graft in Posterior Colporrhaphy

The goal of this clinical trial is to test the benefit of using gamma-irradiated amniotic membrane as a graft in surgical repair for women with posterior vaginal wall defects. The main question it aims to answer is:

• Is posterior colporrhaphy using gamma-irradiated amniotic membrane as a graft effective?

Participants will undergo posterior colporrhaphy, which will be modified by adding gamma-irradiated amniotic membrane as a graft during the repair.

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Key information

Age range

30 year–60 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 3

Primary location

Ain Shams Maternity Hospital

Cairo, Egypt

About this study

  • Methodology:
  • Protocol approval will be sought from the research ethical committee.
  • Enrolment: The patients will be recruited from the outpatient gynecology clinic of Ain Shams University Maternity Hospital (ASUMH).
  • History, examination, and routine investigations will be done to identify eligible patients.

History taking including (personal history, age, menopausal, medical history, and surgical history), as well as symptoms score using Pelvic Organ Prolapse Distress Inventory 6 (POPDI-6) part of the Pelvic Floor Distress Inventory Short Form 20. Also, sexual function will be assessed by Female Sexual Function Index Questionnaire.

Clinical examination: including (general examination, abdominal examination and pelvic examination and POP-Q.

Routine investigations: complete blood count and other preoperative tests as needed.

  • Written informed consent will be sought from the patients after proper counseling.
  • Surgical procedure:

Posterior colporrhaphy with application of the amniotic membrane graft will be done as follows:

Steps of conventional posterior colporrhaphy:

  • A midline incision is extended from the perineal body to the vaginal apex or to the cephalad border of a small or distal rectocele.
  • The Denonvillier's fascia is mobilized from the vaginal epithelium, leaving as much of the tissue as possible attached laterally to the levator fascia.
  • Gamma irradiated Sterilized freeze-dried (lyophilized) amnion grafts will be obtained from the Egyptian Atomic Energy Authority and prepared according to the method of Antounians (2019). Multiple procedures are used to sterilize acellular amniotic membranes, the final of which being gamma irradiation. For tissue allograft sterilisation, gamma radiation is claimed to be the most reliable and successful method. Many tissue banks have employed it to sterilise tissues. The clinical function of the amniotic membrane is unaffected by gamma radiation 11. The most frequent dose for sterilising medical goods is 25 kilogram. This graft has the advantage of complete sterilization and is valid on shelf for 5 years as it is dried. Posterior vaginal wall amniotic membrane graft can be placed on the posterior vaginal wall, between the rectal fascia and the vagina, anchored distally at the uterosacral ligaments, and dorsally at the levator ani muscle. The excess amniotic membrane graft is trimmed off, usually around 1-2 cm on each side.
  • After obvious defects in the rectal muscularis are repaired, the fascia is plicated in the midline with interrupted or continuous sutures using vicryl 0 sutures.
  • When a defective perineal body or perineal membrane is present, reconstruction is performed after accompanying posterior colporrhaphy.
  • The superficial muscles of the perineum and bulbocavernous fascia are plicated in the midline and the skin closed as in an episiotomy repair using vicryl 2/0 sutures.
  • Detachments of the inferior portion of the Denonvillier's fascia from the perineal body are also corrected.

Postoperative instructions and care:

  • Vaginal pack will be left as a compression and will be removed the following day.
  • Urinary catheter: will be left for 24hours then removed.
  • Postoperative clinical assessment by POP-Q.
  • Patients will be instructed to:
  • Mobilize to reduce risk of deep vein thrombosis.
  • Bath or shower as normal routine.
  • Avoid using tampons for 6 weeks.
  • Avoid sexual intercourse for at least 6weeks.
  • Avoid constipation; by drinking plenty of water and fluids, eating fruit and green vegetables, and any constant cough is to be treated promptly.
  • Avoid heavy lifting to reduce the risk of the prolapse recurrence.
  • Follow up schedule:

Follow up of all patients will be done in both groups at 3 and 6 months (symptoms +/- examination as needed).

  • Data collection and recording. Data will be collected and recorded in case report form. Detection bias will be avoided by blinding the outcome assessor.
  • Statistical analysis will be done to get the results.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Women diagnosed as posterior vaginal wall prolapse: bulging of front wall of rectum into the vagina due to weakening of pelvic support system and thinning of rectovaginal septum.
  • Women aged 30-60 years.
  • BMI 20-35 kg/m2
  • Planned for surgical correction

Exclusion criteria

  • Patients with:
  • Immuno-compromise e.g. Patients receiving chemotherapy, steroids.
  • Severe anaemia (Hb<10)
  • conditions that require concomitant reconstructive pelvic floor surgery e.g., anterior and/or apical compartment prolapse.
  • Conditions that lead to increase intra-abdominal pressure e.g.,chronic obstructive pulmonary disease.
  • Uncontrolled medical disorders (diabetes, hypertension, asthma).

Treatment and study plan

posterior colporrhaphy using gamma-irradiated amniotic membrane as a graft

Combination Product

Posterior colporrhaphy with application of the gamma-irradiated amniotic membrane graft will be done

Primary outcomes

  1. POP-Q

    Time frame: first week postoperative

    Prolapse assessment using the prolapse quantification system of the International Continence Society (POP-Q)

  2. POPDI-6 score

    Time frame: at 3 months, and at 6 months postoperative

    Assessment of symptoms score using Pelvic Organ Prolapse Distress Inventory 6 (POPDI-6) part of the Pelvic Floor Distress Inventory Short Form 20. Scale from 0 to 100, the higher score indicates worse condition.

Secondary outcomes

  1. sexual satisfaction

    Time frame: at 3 months, and at 6 months postoperative

    to measure sexual satisfaction using female sexual function index questionnaire The Female Sexual Function Index (FSFI) was developed to assess six domains of female sexual function (sexual desire, sexual arousal, lubrication, orgasm, satisfaction, and pain).

    Items are scored on a five-point Likert scale with low scores indicating lower levels of sexual functioning. Fifteen items also include a zero score as a sixth response option indicating no sexual activity in the past 4 weeks.

    Range: 2 to 36.

  2. wound complications

    Time frame: within 6 months postoperative

    Wound infection or wound dehiscence as detected clinically and /or CRP and vaginal swab as needed

  3. Intraoperative complications

    Time frame: Intraoperative

    occurrence of intraoperative bladder or bowel injury

Sponsors and collaborators

Lead sponsor

Ain Shams Maternity Hospital

Other

Registry information

Official study title

Gamma-irradiated Amniotic Membrane Graft in Posterior Colporrhaphy. A Pilot One Arm Clinical Trial

Important dates

Study start
2023
Primary completion
2025
Study completion
2025
First posted
Nov 7, 2023
Registry last updated
Dec 2, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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