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RECRUITING
NCT07808229
NA

Comprehensive Assessment System for Fallopian Tube Function and Clinical Study on Individualized Treatment Strategies

Sponsor: Peking University People's Hospital

View on ClinicalTrials.gov

Summary

This clinical study aims to develop a comprehensive system to evaluate tubal function and to optimize individualized treatment strategies for patients with tubal factor infertility (caused by hydrosalpinx, obstruction, or adhesions). It will also assess whether integrating novel diagnostic tools, surgical techniques, and anti-adhesion materials can improve pregnancy outcomes. The main questions it aims to answer are: Can a new multi-dimensional evaluation system (combining imaging, ultrasound biomarkers, and surgical scoring) more accurately diagnose tubal damage compared to traditional hysterosalpingography (HSG) alone? Does the combination of improved surgical techniques (laparoscopic recanalization) with a novel anti-adhesion material (chitosan hydrogel) increase the 12-month natural pregnancy rate after surgery compared to historical conventional surgery? Can a prediction model using machine learning accurately predict natural pregnancy within 12 months after tubal surgery and help determine the optimal timing for transitioning to assisted reproductive technology (IVF/ICSI)? Researchers will compare the new evaluation system against the traditional HSG approach, and the optimized surgical procedure with anti-adhesion material against historical data from conventional surgery. Participants in this study will: Undergo pre-operative imaging (HSG, 3D vascular ultrasound) and provide blood samples for biomarker testing (Part 1, n=120) Receive either the new comprehensive tubal function assessment (combining HSG, ultrasound, intraoperative scoring, and biomarkers) or traditional HSG evaluation during the same hospital stay (Part 1) Undergo the optimized laparoscopic tubal surgery with anti-adhesion material application (Part 2, n=120) and be followed up for 12 months to record natural pregnancy Have their clinical data, imaging, and surgical findings used to develop and validate a predictive model for post-surgery natural pregnancy (Part 3, retrospective cohort of \~650 patients and prospective validation of \~200 patients) Complete follow-up visits at 12 months post-surgery to confirm pregnancy status via ultrasound or medical records

Key Details

Gender

FEMALE

Age Range

20 Years - 40 Years

Study Type

INTERVENTIONAL

Enrollment

240

Start Date

2026-08-01

Completion Date

2028-12-31

Last Updated

2026-09-08

Healthy Volunteers

No

Interventions

PROCEDURE

Optimize the techniques and plans for fallopian tube reconstruction surgery

Comprehensive application of interventional recanalization and of anti-adhesion materials

Locations (1)

Peking University People's Hospital

Beijing, Beijing Municipality, China