Clinical Trials Directory

Trials / Completed

CompletedNCT03942250

Uses of Irradiated Human Amniotic Membrane in the Treatment of Dystrophic Epidermolysis Bullosa Patients

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
8 (actual)
Sponsor
Egyptian Atomic Energy Authority · Other Government
Sex
All
Age
12 Years – 45 Years
Healthy volunteers
Accepted

Summary

To evaluate the effect of human amniotic membrane as a weekly dressing on chronic wounds in Epidermolysis Bullosa (EB) patients.

Detailed description

Dried human amniotic membrane dressing were obtained from National center for radiation research and technology, Egypt (NCRRT), under commercial name REGE pro.

Conditions

Interventions

TypeNameDescription
BIOLOGICALREGE pro dressingREGE pro is a dressing of dried human amniotic membrane sterilized by gamma radiation

Timeline

Start date
2017-01-01
Primary completion
2017-12-01
Completion
2019-02-01
First posted
2019-05-08
Last updated
2023-09-21

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT03942250. Inclusion in this directory is not an endorsement.