CTRI/2020/11/029112Completed未知
An observational study of women undergoing ultrasound guided invasive procedures for prenatal diagnosis: miscarriage rate and pregnancy outcome.
nil0 sites150 target enrollmentStarted: TBDLast updated:
Trial Snapshot
- Phase
- 未知
- Status
- Completed
- Sponsor
- Enrollment
- 150
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Observational
Eligibility Criteria
Inclusion Criteria
- •Women with a singleton or multiple pregnancy undergoing an invasive prenatal diagnostic
- •procedure for various indications like
- •i. Positive screening test for aneuploidy (combined screen in the first trimester,
- •quadruple screen in the second trimester and NIPT in the first or second trimester)
- •ii. Soft markers or a structural fetal anomaly detected on ultrasound
- •iii. History of chromosomal anomaly or genetic defect in previous born child
- •iv. Couple who is a known carrier of a genetic disorder
Exclusion Criteria
- •i. History of bleeding In last two weeks preceding planed procedure.
- •ii. History of fever in the last 7 days before procedure.
- •iii. Short cervical length (<= 25 mm) on transvaginal ultrasound in the second trimester
- •or women with cervical cerclage in-situ
- •iv. History of uncontrolled diabetes, hypertension, history of vaginal discharge
- •suggestive of vaginitis.
Investigators
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