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NCT04702399: PREVENDO

Hyaluronic Acid for the Prevention of Endocavitary Synechiae After Myomectomy

Status unknown NA Last updated 8 January 2021
What this trial tests

NA trial testing GEL GROUP in Patients With an Indication for Myomectomy or Polymyomectomy in 76 participants. Status unknown.

Timeline
1 February 2021
Primary endpoint
1 May 2022
1 May 2022

Quick facts

Lead sponsorAssistance Publique - Hôpitaux de Paris
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposeprevention
Enrollment76
Start date1 February 2021
Primary completion1 May 2022
Estimated completion1 May 2022

Drugs / interventions tested

Conditions studied

Sponsor

Assistance Publique - Hôpitaux de Paris — full company profile →

Who can join

18 and older, female only, with Patients With an Indication for Myomectomy or Polymyomectomy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

PREVENDO is a prospective, multicenter, pilot, and randomized study in 2 parallel arms and single blind, evaluating the proportion of endometrial synechiae 6 weeks after surgery in patients undergoing abdominal myomectomy or polymyomectomy, according to the application or not of an anti-adhesion gel (HYALOBARRIER® GEL ENDO)

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other Assistance Publique - Hôpitaux de Paris trials

Trials by the same sponsor.

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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/NCT04702399.

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