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NCT05632250: MORGEN

A Prospective, Multi Centre, Interventional, Non-comparator, Open Label Study to Demonstrate the Efficacy, Safety, and Performance of ConvaFoam™ Dressings in the Management of Indicated Chronic Wound Types.

Completed NA Last updated 30 April 2024
What this trial tests

NA trial testing ConvaFoam in Chronic Ulcer of Leg or Foot in 95 participants. Completed in 13 March 2024.

Timeline
10 April 2023
Primary endpoint
13 March 2024
13 March 2024

Quick facts

Lead sponsorConvaTec Inc.
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment95
Start date10 April 2023
Primary completion13 March 2024
Estimated completion13 March 2024
Sites5 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

ConvaTec Inc.

Who can join

18 and older, any sex, with Chronic Ulcer of Leg or Foot or Pressure Injury. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

A prospective, multi centre, interventional, non-comparator, open label study to demonstrate the efficacy, safety, and performance of ConvaFoam™ dressings in the management of indicated chronic wound types.

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 ConvaFoam

Trials testing the same drug.

Other ConvaTec Inc. 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/NCT05632250.

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