Niche In CEsarean Scar Trial (NICEST)
Recruiting
N/A
Interventional Study
Niche
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.
At a Glance
- Age
- 18 – 60
- Sex
- Female
- Study type
- Interventional
- Purpose
- Prevention
- Participants needed
- 938 (estimated)
- Sponsor
- Nguyen Thi Thu Ha · Other
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About This Trial
Rationale: Cesarean delivery (CD) rates are increasing rapidly worldwide. The consequences of cesarean section not only affect the next pregnancies such as uterine rupture or malplacentation but also cause many gynecological complications or infertility due to the formation of cesarean scar defect (CSD) or Niche. One of the major factors for Niche formation is the techniques of hysterotomy closure…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Pregnant women who undergo a primary CD (planned or unplanned)
* Age ≥ 18 years.
* Gestational age ≥ 37 0/7 weeks
Exclusion Criteria:
* Previous major uterine surgery (e.g. laparoscopic or laparotomic fibroid resection, septum resection).
* Women with abnormal menstrual blee…
Contacts