Clinical Trials in Egypt / NCT07067593
Starting soon
Observational
Amnioreduction in Polyhydramnios
NCT07067593 · tracked via the Priya Life Science Egypt tracker
Condition(s) studied
Polyhydramnios
Study summary
The aim of this work is to review the indications, procedural complications and outcomes of amnioreduction in pregnancies complicated by polyhydramnios.
Eligibility
Inclusion Criteria:
* Pregnant women 20- 38 weeks
* Patients with polyhydramnios
Exclusion criteria:
* Lethal fetal anomalies
* Pre labor rupture of membranes
* Placental separation
* Chorioamnionitis
Primary outcome measure(s)
- Gestational age at delivery — 4 months
Determine Gestational age at delivery in polyhydramnios patients . Increased age is good. - Rate of PROM — 4 months
Number of cases developed PROM
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Women's Health Hospital | Asyut | Egypt |
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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 NCT07067593 on ClinicalTrials.gov ↗ ← All trials in Egypt