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NCT05414760: CLEAN

Evaluate Formation of IUAs After Third-generation Endometrial Ablation, With and Without Intrauterine Adhesion Barrier

Completed NA Last updated 7 February 2024
What this trial tests

NA trial testing Womed Leaf in Asherman Syndrome in 1 participant. Completed in 5 February 2024.

Timeline
11 November 2022
Primary endpoint
5 February 2024
5 February 2024

Quick facts

Lead sponsorRemko P. Bosgraaf
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposeprevention
Enrollment1
Start date11 November 2022
Primary completion5 February 2024
Estimated completion5 February 2024
Sites2 locations across Netherlands

Drugs / interventions tested

Conditions studied

Sponsor

Remko P. Bosgraaf

Who can join

30 and older, female only, with Asherman Syndrome or Intrauterine Adhesion. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Evaluate the formation of adhesions after third-generation endometrial ablation, with and without the intrauterine adhesion barrier.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other trials of Womed Leaf

Trials testing the same drug.

Other recruiting trials for Asherman Syndrome

Currently open trials in the same condition.

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/NCT05414760.

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