To Evaluate the Safety and Effectiveness of Intrauterine Adhesion Preventer in the Prevention and Treatment of Intrauterine Adhesions, a Prospective, Multicenter, Randomized Controlled Clinical Trial

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age20-40
SponsorThe Third Xiangya Hospital of Central South University

About this trial

To evaluate the effect of uterine stents in preventing intrauterine adhesions after intrauterine operation and whether they meet the safety requirements for clinical use. The trial adopted a prospective, multicenter, randomized controlled, non-inferiority clinical trial design. The target population of the trial was 200 women aged 20-40 years with intrauterine adhesions and surgical indications (referring to those with fertility requirements or menstrual blood drainage obstruction), who were randomly divided into an experimental group and a control group, with 100 cases in each group. The experimental group was the group with intrauterine stents placed in the uterine cavity after hysteroscopic intrauterine adhesion separation surgery, and the control group was the group with intrauterine rings + balloons + sodium hyaluronate gel placed in the uterine cavity. After 3 courses of artificial cycles, the patients were hospitalized for hysteroscopy review.

Eligibility criteria

Qualifiers

Patients clinically diagnosed with intrauterine adhesions and with surgical indications (referring to those with fertility requirements or obstructed menstrual blood drainage) ② Women aged 20-40 years old; ③ Subjects voluntarily participated in the trial and signed informed consent.

Disqualifiers

① Patients with obviously abnormal uterine cavity shape after surgery; those who could not clearly separate the normal uterine cavity anatomical morphology (i.e. bilateral or unilateral fallopian tube openings were not visible); those with reproductive organ malformations and uterine cavities that were too large or too small; those with recent uterine perforation; those with cervical insufficiency.

Those with a history of intrauterine adhesions and treatment;

Those with endometrial tuberculosis or suspected endometrial tuberculosis;

Those with adenomyosis or uterine fibroids>4cm;

Trial design

Treatments tested in this trial

  • Uterine stent group
  • Uterine ring + balloon + sodium hyaluronate gel

Treatment groups

200 Participants
are divided into 2 treatment groups

Sponsors and collaborators

The Third Xiangya Hospital of Central South University

Lead sponsor

Hunan Haokang Medical Technology Co., Ltd.

Collaborator

Beijing Tiantan Hospital

Collaborator

The First Affiliated Hospital of Hunan University of Traditional Chinese Medicine

Collaborator