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NCT Number: NCT06508151

Neovaginoplasty Using Photoinduced-imine-crosslink Hydrogel in MRKH Patients

Evaluating the effectiveness and safety of neovaginoplasty using photoinduced-imine-crosslink hydrogel in patients with MRKH syndrome by comparing the differences in the degree of squamous epithelialization, vaginal length and width, and sexual life quality.

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Key information

Age range

18 year–35 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

About this study

This is a randomized controlled trial. Patients meeting the inclusion criteria will be enrolled in this study: 1)Diagnosed with MRKH syndrome; 2)Without previous treatments; 3)Age: 18-35 years old; 4)Voluntary agreement to participate in the study, sign the informed consent form, and demonstrate good compliance with follow-up.

A centralized block randomization will be used to randomly assign patients to ensure that there will be an equal number of patients (1:1) in the hydrogel group and control group. The sample size is 20.

Under general anesthesia and catheterized bladder, the patient was in the lithotomy position. In the connective tissue plane between the bladder and rectum, the vestiges of the müllerian ducts were identified. With the index finger in the rectum as a direction and protection, Hegar's dilators of increasing size (4.5-10) were pushed through the dimples gently. After that, a double-barreled canal appeared. Then, the raphe between the canals was incised. The neovagina was created. According to the randomization, a vaginal mold spreaded with hydrogel or not was placed. The patients were suggested to wear the vaginal mold continuously over the following 6 months. After that, they were allowed to have the first sexual intercourse. Otherwise, the mold wearing time was 1 h daily, until they had sexual activity at least twice a week.

The primary endpoint is the degree of vaginal squamous epithelialization 1 month, 3 months, 6 months after surgery. The secondary endpoints include neovaginal length and width, sexual life quality, and surgical complications.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Diagnosed with MRKH syndrome;
  • Without previous related treatments; 3)18-35 years old;

4)Voluntary agreement to participate in the study, sign the informed consent form, and demonstrate good compliance with follow-up.

Exclusion criteria

  • With any previous artificial colpoplasty or other related treatment;
  • With history of diabetes or systemic immune system disease.

Treatment and study plan

neovaginoplasty and vaginal mold spreaded with photoinduced-imine-crosslink hydrogel

Procedure

Under general anesthesia and catheterized bladder, the patient was in the lithotomy position. In the connective tissue plane between the bladder and rectum, the vestiges of the müllerian ducts were identified. With the index finger in the rectum as a direction and protection, Hegar's dilators of increasing size (4.5-10) were pushed through the dimples gently. After that, a double-barreled canal appeared. Then, the raphe between the canals was incised. The neovagina was created. According to the randomization, a vaginal mold spreaded with hydrogel or not was placed in the neovagina for 6 months. The patients were suggested to wear the vaginal mold continuously over the following 6 months. After that, they were allowed to have the first sexual intercourse. Otherwise, the mold wearing time was 1 h daily, until they had sexual activity at least twice a week.

neovaginoplasty and vaginal mold

Procedure

Under general anesthesia and catheterized bladder, the patient was in the lithotomy position. In the connective tissue plane between the bladder and rectum, the vestiges of the müllerian ducts were identified. With the index finger in the rectum as a direction and protection, Hegar's dilators of increasing size (4.5-10) were pushed through the dimples gently. After that, a double-barreled canal appeared. Then, the raphe between the canals was incised. The neovagina was created. According to the randomization, a vaginal mold spreaded with hydrogel or not was placed in the neovagina for 6 months. The patients were suggested to wear the vaginal mold continuously over the following 6 months. After that, they were allowed to have the first sexual intercourse. Otherwise, the mold wearing time was 1 h daily, until they had sexual activity at least twice a week.

Primary outcomes

  1. Degree of vaginal squamous epithelialization

    Time frame: 1 month

    Percentage of squamous epithelialization of neovagina

  2. Degree of vaginal squamous epithelialization

    Time frame: 3 months

    Percentage of squamous epithelialization of neovagina

  3. Degree of vaginal squamous epithelialization

    Time frame: 6 months

    Percentage of squamous epithelialization of neovagina

Secondary outcomes

  1. length of neovagina

    Time frame: 1 month

    length in centimetre, measured by a ruler

  2. length of neovagina

    Time frame: 3 months

    length in centimetre, measured by a ruler

  3. length of neovagina

    Time frame: 6 months

    length in centimetre, measured by a ruler

  4. width of neovagina

    Time frame: 1 month

    width in centimetre, measured by ruler

  5. width of neovagina

    Time frame: 3 months

    width in centimetre, measured by ruler

  6. width of neovagina

    Time frame: 6 months

    width in centimetre, measured by ruler

  7. Sexual life quality

    Time frame: 6 months

    Female Sexual Function Index, a self-reported questionnaire to measure sexual life quality

  8. Sexual life quality

    Time frame: 1 year

    Female Sexual Function Index, a self-reported questionnaire to measure sexual life quality

Study contacts

Contact information is provided by the study sponsor or research team.

Keqin Hua, Doctor

CONTACT

[email protected]

+86-021-33189900

Sponsors and collaborators

Lead sponsor

Obstetrics & Gynecology Hospital of Fudan University

Other

Registry information

Official study title

Study on the Effectiveness and Safety of Neovaginoplasty Using Photoinduced-imine-crosslink Hydrogel in Patients With Mayer-Rokitansky-Kuster-Hauser Syndrome

Important dates

Study start
2024
Primary completion
2025
Study completion
2026
First posted
Jul 18, 2024
Registry last updated
Jul 18, 2024

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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