Study of Donated Amnion, Fetal Placental Membrane, as Skin Substitute for Burn Patients

Is the use of fetal membrane (human amnion) as a transient wound coverage in wound repair safe and efficacious.

Will the incorporation of liposomal gene constructs to amnion enhance the functionality of human amnion and improve wound repair.

Completed

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Key information

Conditions

Wounds Burns Wounds and Injuries

Age range

16 year–65 year

Sex eligibility

Female

Study type

Interventional

Phase

Early Phase 1

Primary location

University of Texas Medical Branch

Galveston, Texas, 77555, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Women
Pregnant, delivery expected within the month

Exclusion criteria

Known history of hepatitis, HIV, or active transmissable diseases

Treatment and study plan

Blood draw

Procedure

blood collection

Primary outcomes

Safe method of obtaining and processing amnion

Time frame: 0-21 days post harvest

Sponsors and collaborators

Lead sponsor

The University of Texas Medical Branch, Galveston

Other

Registry information

Official study title

Fetal Membrane as a New Coverage Material

Acronym: Amnion

Important dates

Study start: 1999
Primary completion: 2014
Study completion: 2014
First posted: Jan 11, 2008
Registry last updated: Jun 24, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed