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Clinical Trials in China / NCT07610668
Recruiting Observational

Clinical Value of Saline Infusion Sonohysterography in the Assessment of Cesarean Scar Defects

NCT07610668 · tracked via the Priya Life Science China tracker
Sponsor
Tang-Du Hospital
Phase
Observational
Started
2023-01-01
Last updated
2026-05-28

Condition(s) studied

Infertility

Investigational drug(s) / intervention(s)

diverticulum reconstruction surgery

diverticulum reconstruction surgery: This group of patients received conventional infertility treatment only, without undergoing diverticulum reconstruction surgery, in accordance with standard clinical practice.

Study summary

This study selected patients who underwent cesarean section and were scheduled to undergo Saline Infusion Sonohysterography (SIS) for evaluating the structure of the incision. Clinical characteristics and clinical symptoms were collected. Combined with hysteroscopy, MRI, conventional ultrasound and SIS examination results, the study analyzed the detection rate of cesarean section diverticula by SIS, the changes in diverticulum size and the diagnostic efficacy of residual muscle layer thickness at the incision site. The surgical methods and clinical symptom improvement of patients with CSD after surgery were followed up for half a year to one year. The study aimed to clarify the guiding value of SIS in clinical decision-making and patient prognosis for patients, and to analyze the etiological relationship between the true incidence of CSD and clinical complications. Thus, it provided evidence-based basis for clinical events of cesarean section surgery → CSD → CSD complications → surgical treatment of CSD → patient prognosis, promoting the progress of precise diagnosis and treatment of female reproductive health.

Eligibility

Sex
FEMALE
Min age
20 Years
Max age
50 Years
Healthy volunteers
Accepted
Inclusion Criteria: * More than 6 months after cesarean delivery; * Presenting with clinical symptoms-including abnormal uterine bleeding, dysmenorrhea, prolonged menstrual spotting, or secondary infertility; * Requiring saline infusion sonohysterography (SIS) to evaluate the cesarean scar. Exclusion Criteria: * Multiple cesarean deliveries; * Patients contraindicated for saline infusion sonohysterography (SIS), including pregnancy or suspected pregnancy, failure to meet vaginal hygiene criteria, inability to cooperate during the procedure, or suboptimal image quality; * Cases with incomplete clinical data or lost to follow-up.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Tang-Du Hospital Xi'an Shaanxi Recruiting

More Tang-Du Hospital trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07610668 on ClinicalTrials.gov ↗ ← All trials in China