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NCT04516226

Vaginal Cleansing With Chlorhexidine Gluconate in Women With Preterm Pre-labor Rupture of Membranes

Status unknown NA Last updated 18 April 2023
What this trial tests

NA trial testing Vaginal cleansing with chlorhexidine gluconate solution in Preterm Premature Rupture of Membrane in 40 participants. Status unknown.

Timeline
1 August 2020
Primary endpoint
31 December 2024
31 December 2024

Quick facts

Lead sponsorAlbany Medical College
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment40
Start date1 August 2020
Primary completion31 December 2024
Estimated completion31 December 2024
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Albany Medical College

Who can join

Adults 18 to 50, female only, with Preterm Premature Rupture of Membrane. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Randomized controlled trial studying the use of vaginal cleansing with chlorhexidine gluconate for pregnant women with PPROM (preterm pre labor rupture of membranes). The primary outcome will be pregnancy latency. Secondary outcomes will include various maternal and neonatal outcomes, and inflammatory markers from maternal blood, amniotic fluid, fetal cord blood and placental analysis.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Preterm Premature Rupture of Membrane

Currently open trials in the same condition.

Other Albany Medical College trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04516226.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing