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NCT03739463: Pro-MEGA

Pro-omega-3, Reduction of Inflammation and Modulation of Prematurity

Status unknown NA Last updated 20 November 2018
What this trial tests

NA trial testing MAG-DHA in PPROM in 70 participants. Status unknown.

Timeline
3 December 2018
Primary endpoint
5 November 2019
15 May 2020

Quick facts

Lead sponsorUniversité de Sherbrooke
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposeother
Enrollment70
Start date3 December 2018
Primary completion5 November 2019
Estimated completion15 May 2020

Drugs / interventions tested

Conditions studied

Sponsor

Université de Sherbrooke — full company profile →

Who can join

Adults 18 to 42, female only, with PPROM. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The aim of the project is to decrease the inflammatory status of pregnant women with preterm premature rupture of membranes to delay the initiation of labour that would inevitably lead to premature delivery. The main objective is to measure the mean duration between the initiation of the treatment and delivery in the two groups treated either with MAG-DHA or with the placebo.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for PPROM

Currently open trials in the same condition.

Other Université de Sherbrooke 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/NCT03739463.

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