Standardized Prenatal Clinical Care for LUTO
Recruiting
Observational Study
Urethral Obstruction
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 11 Weeks – 2
- Sex
- Any
- Study type
- Observational
- Participants needed
- 50 (estimated)
- Sponsor
- Baylor College of Medicine · Other
Who this trial is looking for
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About This Trial
The investigators propose a standardized prenatal management, based on the scientific evidence published in the literature, to manage prenatally fetuses with lower urinary tract obstruction (LUTO). The present study is a prospective registry that will evaluate and validate this standardized prenatal management for LUTO.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
\- Pregnant women whose fetuses have diagnosis of LUTO independently from the gestational age at diagnosis.
Exclusion Criteria:
* Presence of abnormal chromosomal/genetic disease
* Presence of other associated structural anomaly that is not part of LUTO.
Inclusion Criteria:
\- Pregnant women whose fetuses have diagnosis of LUTO independently from the gestational age at diagnosis.
Exclusion Criteria:
* Presence of abnormal chromosomal/genetic disease
* Presence of other associated structural anomaly that is not part of LUTO.