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NCT05632250 · ClinicalTrials.gov registry record · NA

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.

A NA study, sponsored by ConvaTec.

Completed
Registry status
NA
Development phase
95
Enrollment target

NCT05632250: Completed NA study, sponsored by ConvaTec.

NCT05632250 is a NA study that has completed, run by ConvaTec. The registered enrollment target is 95 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (93% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05632250, a NA study, has completed, sponsored by ConvaTec.

COMPLETED
Registry status
NA
Development phase
95 participants
Enrollment target

Study Summary

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.

Primary Outcome

This will be measured by: Lack of strike through Loss of edge seal/adherence, Dressing leakage/seepage Dislodgement Need for dressing change

Interventions

  • DEVICE ConvaFoam

Trial Details

FieldValue
Enrollment Target 95 participants
Start Date 2023-04-10
Est. Completion 2024-03-13
Phase NA
ConvaTec

17 total trials

What the finished NCT05632250 record still lists

NCT05632250 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 95 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (93% lower).

The record links to 0 conditions, and to 1 intervention - of which ConvaFoam is the first listed.

NCT05632250 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05632250 about?

NCT05632250 is a clinical study titled "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.". 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.

What is the current status of trial NCT05632250?

This trial is currently completed. It is a NA study. The enrollment target is 95 participants. The study started on 2023-04-10. Estimated completion is 2024-03-13.

What interventions are being tested in trial NCT05632250?

The interventions under investigation include: ConvaFoam (DEVICE).

Who is sponsoring clinical trial NCT05632250?

This trial is sponsored by ConvaTec, which has 17 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05632250's enrollment target sits among peer trials

95 931st of 2000 higher than 1,066 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05632250, the US trial registry maintained by the National Library of Medicine. NCT05632250 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.