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Uses of Gamma Irradiated Amniotic Membrane as an Alternative Method in Psoriasis Treatment

Uses of Gamma Irradiated Amniotic Membrane as an Alternative Method in Psoriasis Treatment

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03440541
Enrollment
22
Registered
2018-02-22
Start date
2015-08-04
Completion date
2016-04-08
Last updated
2019-06-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Psoriasis

Keywords

Amniotic membrane, Psoriasis, Treatment

Brief summary

Using of human amniotic membrane extra-cellular matrix as a topical treatment for improving Psoriasis Area and Severity Index (PASI).

Detailed description

Human amniotic membrane extra-cellular matrix was purchased from National center for radiation research and technology, Egypt, under commercial name REGE pro gel.

Interventions

COMBINATION_PRODUCTREGE pro

REGE pro is a patch of human amniotic membrane sterilized by gamma radiation

Sponsors

Egyptian Atomic Energy Authority
Lead SponsorOTHER_GOV

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* patients have psoriasis lesion

Exclusion criteria

* must stop other line of treatment

Design outcomes

Primary

MeasureTime frameDescription
Scaling size decrement2 weeksREGE pro gel decreased scaling size in patients with sever scales to moderate scale within two weeks, scaling size decrement from moderate to mild within two weeks, and from mild to complete curing within two weeks
Histopathological improvement6 weeksTwo biopsies were taken from each patient before and at the end of the treatment. It was noted that all histological signs as munro's microabscess and the elongation of rete ridges were absent.

Secondary

MeasureTime frameDescription
Erythema disappearing4-6 weeksREGE pro gel gradually decreased erythema in patients within 4-6 weeks, these data were collected from applied patients by questionnaire.

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026