Last reviewed · How we verify

NCT00714519

A Phase II Feasibility Study of Xenaderm® Ointment Exploring Design Issues for Phase III Efficacy in Partial-Thickness Wounds

Withdrawn Phase 2 Last updated 29 August 2013
What this trial tests

Phase 2 trial testing Xenaderm® Ointment in Partial Thickness Wounds. Withdrawn.

Timeline
1 July 2008
Primary endpoint
1 October 2008
1 October 2008

Quick facts

Lead sponsorHealthpoint
PhasePhase 2
StatusWithdrawn
Study typeINTERVENTIONAL
Allocationrandomized
Designsingle group
Maskingtriple
Primary purposetreatment
Start date1 July 2008
Primary completion1 October 2008
Estimated completion1 October 2008

Drugs / interventions tested

Conditions studied

Sponsor

Healthpoint — full company profile →

Who can join

18 and older, any sex, with Partial Thickness Wounds. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

This study will assess if a clinical trial regarding healing of partial thickness wounds can be executed in nursing homes.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

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/NCT00714519.

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