Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT06751264

Evaluation of the Efficacy and Safety of Microwave Ablation of Uterine Adenomyosis Under Improved Ultrasound Guidance

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
137 (estimated)
Sponsor
Peking University Aerospace Center Hospital · Academic / Other
Sex
Female
Age
18 Years – 60 Years
Healthy volunteers
Not accepted

Summary

This study aims to compare the safety and efficacy of segmental power adjustment combined with uterine cavity hydro-isolation in microwave ablation of adenomyosis

Conditions

Interventions

TypeNameDescription
PROCEDUREPeritoneal combined with intrauterine water isolationOn the basis of the conventional peritoneal water isolation group, the improved technology group added additional intrauterine water isolation, and continued to inject ice saline to separate the endometrium on both sides.
PROCEDUREPeritoneal water isolationTransabdominal injection of saline into the abdominal cavity to achieve complete separation of the uterus from the surrounding organs and structures

Timeline

Start date
2025-01-01
Primary completion
2027-12-31
Completion
2027-12-31
First posted
2024-12-27
Last updated
2024-12-27

Source: ClinicalTrials.gov record NCT06751264. Inclusion in this directory is not an endorsement.