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Completed

NCT Number: NCT03353909

The Efficacy of A New Crosslinked Hyaluronan Gel in Prevention of Intrauterine Adhesion

Using American Fertility Society classification of intrauterine adhesions, the efficacy of a new crosslinked hyaluronan gel in reducing intrauterine adhesion formation after dilatation and curettage for delayed miscarriage in women without previous dilatation and curettage was examined.

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Key information

Age range

18 year–45 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

About this study

Study Objectives: To evaluate the efficacy of a new crosslinked hyaluronan gel in reducing intrauterine adhesions formation after dilatation and curettage.

Design: Randomized controlled trial. Settings: Six hospitals for maternal and child health care in China. Patients: Three hundred women undergoing dilatation and curettage for delayed miscarriage without previous dilatation and curettage.

Interventions: Women were randomly assigned into either dilatation and curettage alone group or dilatation and curettage plus new crosslinked hyaluronan gel application group with 1:1 allocation.

Measurements and Outcomes: All patients were evaluated using American Fertility Society classification of IUAs during the follow-up diagnostic hysteroscopy, scheduled 3 months after dilatation and curettage procedure. The primary outcome was the number of women with IUAs, and the secondary outcome was the adhesion scores and the severity of IUAs.

Who can participate

Healthy volunteers accepted: No

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

The inclusion criteria:

  • Patients to be female, aged 18-45 years
  • Without previous dilatation and curettage
  • Undergoing dilatation and curettage for the current delayed miscarriage
  • All participants should be with normal liver/rental function and without systemic disease
  • Agree to use adequate forms of contraception throughout the study
  • Be in good compliance with the follow-up examination according to the study protocol.

The exclusion criteria:

  • Known/suspected intolerance or hypersensitivity to hyaluronan or its derivatives
  • Genital tract malformation
  • Inflammation of genital tract or pelvic cavity, clinical evidence of cancer in genital tract
  • Suspected genital tuberculosis
  • Abnormal blood coagulation
  • Medical histories of peripheral vascular disease, alcohol/drug abuse, and mental illness
  • Acute or severe infection
  • Autoimmune diseases.

Treatment and study plan

new crosslinked hyaluronan gel

Device

At the end of the dilatation and curettage, new crosslinked hyaluronan gel was applied to the uterine cavity.

Other names: MateRegen Gel

Primary outcomes

  1. Incidence of intrauterine adhesion

    Time frame: 3 months after dilatation and curettage

    The number of women with intrauterine adhesion

Secondary outcomes

  1. The adhesion scores of extent of uterine cavity involved

    Time frame: 3 months after dilatation and curettage

    Evaluated according to American Fertility Society classification of intrauterine adhesion during the follow-up diagnostic hysteroscopy: 1 point (<1/3 cavity with adhesion), 2 points (1/3-2/3 cavity with adhesion) and 4 points (>2/3 cavity with adhesion), high values represent worse outcome

  2. The adhesion scores of type of adhesion

    Time frame: 3 months after dilatation and curettage

    Evaluated according to American Fertility Society classification of intrauterine adhesion during the follow-up diagnostic hysteroscopy: 1 point (filmy adhesion), 2 points (filmy & dense adhesion) and 4 points (dense adhesion), high values represent worse outcome

  3. The adhesion scores of menstrual pattern

    Time frame: 3 months after dilatation and curettage

    Evaluated according to American Fertility Society classification of intrauterine adhesion during the follow-up diagnostic hysteroscopy: 0 point (normal), 2 points (hypomenorrhea) and 4 points (amenorrhea), high values represent worse outcome

  4. Cumulative adhesion score

    Time frame: 3 months after dilatation and curettage

    The summed score of the adhesion scores of extent of uterine cavity involved, type of adhesion and menstrual pattern; range: 1-12 points, high values represent worse outcome

  5. Severity

    Time frame: 3 months after dilatation and curettage

    Graded according to cumulative adhesion score: Stage I (mild)(1-4 points), Stage II (moderate)(5-8 points) and Stage III (severe)(9-12 points).

Sponsors and collaborators

Lead sponsor

BioRegen Biomedical (Changzhou) Co., Ltd

Industry

Registry information

Official study title

The Efficacy of A New Crosslinked Hyaluronan Gel in the Prevention of Postoperative Intrauterine Adhesion After Dilatation and Curettage in Women With Delayed Miscarriage: A Prospective, Randomized, Controlled Trial

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Nov 27, 2017
Registry last updated
Nov 27, 2017

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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