Clinical Value of Saline Infusion Sonohysterography in the Assessment of Cesarean Scar Defects
Recruiting
Observational Study
Infertility
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 20 – 50
- Sex
- Female
- Study type
- Observational
- Participants needed
- 300 (estimated)
- Sponsor
- Tang-Du Hospital · Other
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About This Trial
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 SI…
Trial Locations
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Eligibility Criteria
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.
Exclus…
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