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NCT00426972

A Double Blind, Placebo Controlled Trial to Investigate the Efficacy of Zesteem (Estradiol) in Accelerating the Healing of Split Thickness Skin Graft Donor Sites.

Completed Phase 3 Last updated 27 August 2009
What this trial tests

Phase 3 trial testing estradiol (Zesteem) in Burn in 148 participants. Completed in 1 October 2008.

Timeline
1 January 2007
Primary endpoint
1 July 2008
1 October 2008

Quick facts

Lead sponsorRenovo
PhasePhase 3
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment148
Start date1 January 2007
Primary completion1 July 2008
Estimated completion1 October 2008
Sites30 locations across Germany, Latvia, Russia, United Kingdom

Drugs / interventions tested

Conditions studied

Sponsor

Renovo — full company profile →

Who can join

Adults 18 to 85, any sex, with Burn or Trauma. 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 trial will assess the effects of Zesteem (estradiol) on the healing of split thickness skin graft donor sites in patients aged 18-85 years.

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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Currently open trials in the same condition.

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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/NCT00426972.

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