To Study the Safety and Efficacy of Disposable Cyclone Ring in Artificial Abortion

Not Applicable

Not yet recruiting

• Conditions: Induced Abortion

• Registration Number: NCT06894732
• Lead Sponsor: Peking Union Medical College Hospital

Brief Summary

The purpose of this study is to compare the two surgical methods of surgical rotation abortion and surgical negative pressure uterine aspiration with the termination of pregnancy. which one can better protect female fertility; To understand the impact of both surgical approaches on the long-term prognosis of patients.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2025-01-25
• Status Verified: 2025-02
• Study First Submitted QC: 2025-03-19
• Last Update Submitted: 2025-03-19
• Study Start: 2025-03-20
• Study First Posted: 2025-03-25
• Last Update Posted: 2025-03-25
• Primary Completion: 2025-12-31
• Study Completion: 2025-12-31

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: Female
• Target Recruitment: 332

Inclusion Criteria

• 1. Age: 20-40 years old, planning to terminate pregnancy; 2) Menopause time≤ 56 days (8 weeks); 3) Ultrasound examination showed early pregnancy in utero, and the average diameter of the fetal sac was 1-3cm; 4) According to the requirements of clinical operation standards, the preoperative examination, laboratory results and surgical indicators are normal 5) The subject was conscious, had good compliance, agreed to participate in the trial, and voluntarily signed the informed consent form

Exclusion Criteria

• 1. According to the requirements of clinical practice, there are contraindications to induced abortion; 2) The number of previous induced abortions ≥2 times; 3) Diseases affecting uterine cavity morphology such as uterine malformations and uterine fibroids; 4) History of uterine surgery: such as submucosal myomectomy history, mediastinal resection history, uterine adhesion-separation history; 5) Unable to sign the informed consent; 6) Other conditions that the investigator considers inappropriate to participate in this clinical study.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Cervical dilation rate (e.g. %)	30

Trial Locations

Locations (1)

Peking Union Hospital, Chinese Academy of Medical Sciences; 🇨🇳 Beijing, Beijing, China