NCT00548210

Brief Summary

The purpose of this research is to demonstrate effectivity of Dermatix in promoting maturation of the scar, versus a control region that will be treated with an indifferent cream.

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
25

participants targeted

Target at below P25 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

October 22, 2007

Completed
1 day until next milestone

First Posted

Study publicly available on registry

October 23, 2007

Completed
Last Updated

October 23, 2007

Status Verified

October 1, 2007

First QC Date

October 22, 2007

Last Update Submit

October 22, 2007

Conditions

Keywords

Hypertrophyscarringscar treatmentsilicone

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Written informed consent
  • Patients of 18 years or older

You may not qualify if:

  • Known sensitivity for occlusive dressings or silicone containing products
  • Any patient condition that may influence the compliance of the treatment negatively.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Association of Dutch Burn Centres

Beverwijk, North Holland, 1940 EB, Netherlands

RECRUITING

MeSH Terms

Conditions

Cicatrix, HypertrophicHypertrophyCicatrix

Condition Hierarchy (Ancestors)

FibrosisPathologic ProcessesPathological Conditions, Signs and SymptomsPathological Conditions, Anatomical

Study Officials

  • Esther Middelkoop, PhD

    Association of Dutch Burn Centres

    STUDY DIRECTOR

Central Study Contacts

Antoon van den Bogaerdt, PhD

CONTACT

Esther Middelkoop, PhD

CONTACT

Study Design

Study Type
observational
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER

Study Record Dates

First Submitted

October 22, 2007

First Posted

October 23, 2007

Last Updated

October 23, 2007

Record last verified: 2007-10

Locations