Clinical trial . gov

To register your clinical trial:. Contact your organization's Clinicaltrials. If you do not know your account administrator, contact register clinicaltrials. You are responsible for maintaining the accuracy of the trial information in ClinicalTrials. To update your trial information:. You are required to submit results of data. It is important to note that results-reporting requires a fairly sophisticated knowledge of the study.

To report your trial results:. Under the FDA Modernization Act, NIH was instructed to establish a database of therapeutic clinical trials that is understandable and accessible to the public.

The purpose of this legislation was to make information about clinical trials available to members of the public who are suffering from diseases so they can apply to be research subjects. A clinical trial also clinical research is a research study in human volunteers to answer specific health questions. Interventional trials determine whether experimental treatments or new ways of using known therapies are safe and effective under controlled environments. Observational trials address health issues in large groups of people or populations in natural settings.

City x. Distance 50 miles miles miles miles. Advanced Search. Researchers Search the database to stay up to date on developments in your field, find collaborators, and identify unmet needs.

Study Record Managers Learn about registering studies and about submitting their results after study completion. National Library of Medicine U. National Institutes of Health U. Study Synopsis Title; The dermis graft: epithelialization and late scar evaluation A Clinical Prospective multicenter trial Objectives; The objective of this study is to compare a dermal graft with a conventional split thickness skin graft regarding healing quality and scarring.

Detailed Description:. FDA Resources. Arms and Interventions. A dermatome will be used for graft harvest. Outcome Measures. Primary Outcome Measures : Healing time [ Time Frame: 4 weeks ] Recipient sites are to be assessed regarding healing re-epithelization at each site donor respective recipient. Healing will be assesed in days after surgery. Eligibility Criteria. Exclusion Criteria: Patients with severe cutaneous trauma at the same site as the burn injury Previous burns at the treatment site Severe cognitive dysfunction or psychiatric disorder Chronic skin disorder Chronic use of systemic or local corticosteroid Chronic use of anticoagulants or platelets Autoimmune disease Active hepatitis Full thickness burns of head, genitalia, axilla or upper third of medial upper arm.

Contacts and Locations. Information from the National Library of Medicine To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor. Please refer to this study by its ClinicalTrials. More Information.

National Library of Medicine U. National Institutes of Health U. Department of Health and Human Services. The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Procedure: Skin transplantation to heal burn injuries.