Status:

RECRUITING

Study on the Effect of Combined Estrogen and Progestogen Therapy on Endometrial Repair After Induced Abortion

Lead Sponsor:

Women's Hospital School Of Medicine Zhejiang University

Conditions:

Pregnancy Complications

Eligibility:

FEMALE

18-40 years

Phase:

PHASE1

Brief Summary

Induced abortion is a common method to terminate pregnancy, but during the operation, it is necessary to dilate the cervix and aspirate the uterine cavity. Repeated induced abortions may increase the ...

Detailed Description

Postoperative care after induced abortion should prioritize the issue of endometrial repair. In 2021, the Family Planning Branch of the Chinese Medical Association published the "Expert Consensus on P...

Eligibility Criteria

Inclusion

  • Age between 18 years old (inclusive) and 40 years old (inclusive)
  • Body Mass Index (BMI) ranging from 18.5Kg/㎡ to 23.9Kg/㎡
  • Experienced at least 2 abortions or had a missed abortion
  • Confirmed gestational age of no more than 10 weeks, and the ultrasonic examination within three days prior to the surgery shows a gestational sac (average of three diameters) of at least 1.0cm, with an embryo length of no more than 3.0cm
  • Normal preoperative examination results as per the "Clinical Diagnosis and Treatment Guidelines and Technical Operation Standards: Family Planning Volume (2017 Revision)"
  • Capable of regular follow-ups and willing to sign the informed consent form.

Exclusion

  • Individuals with contraindications to estrogen and progesterone therapy
  • History of uterine adhesions confirmed by hysteroscopy, or a history of uterine cavity surgery or uterine malformation correction
  • Subjects who require placement of an intrauterine device or administration of oral contraceptives or subcutaneous implants after the procedure
  • Individuals with mental status or cognitive function abnormalities who are unable to cooperate with the treatment process
  • Subjects who, in the opinion of the investigator, have potential risks or any other factors that may interfere with the study.

Key Trial Info

Start Date :

May 9 2024

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

December 31 2025

Estimated Enrollment :

200 Patients enrolled

Trial Details

Trial ID

NCT06546397

Start Date

May 9 2024

End Date

December 31 2025

Last Update

August 28 2025

Active Locations (1)

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1

Women's Hospital School Of Medicine Zhejiang University

Hangzhou, Zhejiang, China, 310006