ClinicalTrials.Veeva

Menu

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

E

Egyptian Atomic Energy Authority

Status

Completed

Conditions

Chronic Skin Ulcer
Epidermolysis Bullosa

Treatments

Biological: REGE pro dressing

Study type

Interventional

Funder types

Other

Identifiers

NCT03942250
2222018NCRRT

Details and patient eligibility

About

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

Full description

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

Enrollment

8 patients

Sex

All

Ages

12 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

1- Patients diagnosed as EB wounds must be chronic

Exclusion criteria

  1. Patients Must stop other line of treatment

  2. Exclude patients have:

    1. Autoimmune diseases
    2. Diabetes

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

8 participants in 1 patient group

Treated
Experimental group
Description:
Patients who received REGE pro dressing on EB wounds lesion weekly for 10 weeks
Treatment:
Biological: REGE pro dressing

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems