Study on the Treatment With Water-filtered Infrared-A (wIRA) Radiation in Patients With Morphea and Sclerotic Graft-versus-host Disease
Primary Purpose
Morphea (Circumscribed Scleroderma), Sclerotic Graft-versus-host Disease (GVHD)
Status
Recruiting
Phase
Not Applicable
Locations
Austria
Study Type
Interventional
Intervention
infrared-A (wIRA)
Sponsored by
About this trial
This is an interventional treatment trial for Morphea (Circumscribed Scleroderma)
Eligibility Criteria
Inclusion Criteria:
- Morphea
- Sclerotic graft-versus-host disease (GVHD)
Exclusion Criteria:
- Inability to cope with the treatment plan
- Pregnant or breastfeeding women and women of childbearing potential without effective contraception
Sites / Locations
- Department of Dermatology, Medical University of GrazRecruiting
- Department of Dermatology, Medical University of ViennaRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Other
Other
Arm Label
Morphea
Sclerotic graft-versus-host disease (GVHD)
Arm Description
Outcomes
Primary Outcome Measures
Intensity of skin sclerosis
as determined by a high-frequency ultrasound device with a 22 MHz applicator
Secondary Outcome Measures
Assessment of skin Score
determined by modified Rodnan Skin Score (mRSS) (range, 0 to 51 )
Assessment of skin hardness
as determined by durometer
Assessment of range of motions
as measured by the range of motions in the presence of contractures (range, 0 to 90 degree)
Grade of patient satisfaction
as determined by Patients' Global Impression of Change (PGIC) scale (range, 0 to 7)
Full Information
NCT ID
NCT04954573
First Posted
June 9, 2021
Last Updated
October 7, 2022
Sponsor
Medical University of Graz
1. Study Identification
Unique Protocol Identification Number
NCT04954573
Brief Title
Study on the Treatment With Water-filtered Infrared-A (wIRA) Radiation in Patients With Morphea and Sclerotic Graft-versus-host Disease
Official Title
Pilot Study on the Treatment With Water-filtered Infrared-A (wIRA) Radiation in Patients With Morphea and Sclerotic Graft-versus-host Disease
Study Type
Interventional
2. Study Status
Record Verification Date
October 2022
Overall Recruitment Status
Recruiting
Study Start Date
July 1, 2021 (Actual)
Primary Completion Date
June 30, 2023 (Anticipated)
Study Completion Date
September 30, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Medical University of Graz
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This is a prospective, intra-individual comparative study to evaluate the effectiveness of local-water filtered infrared-A (wIRA) irradiation (applied by Hydrosun® radiator 750 for radiation at the clinic, or Hydrosun® 575home for home treatment) in patients with morphea or sclerotic GVHD (Graft-versus-host Disease). The purpose of the study is to determine whether wIRA irradiation can reduce fibrotic skin alterations in circumscribed scleroderma (morphea) or chronic graft versus host disease. wIRA irradiation is applied for 30 minutes 3 times per week for 20 weeks to a diseased skin area and a lesional skin on contralateral body site remains untreated. A total of 22 patients (20 evaluable patients with an expected drop-out rate of 10%) are to be included in this study. Group A: 11 patients with plaque morphea Group B: 11 patients with sclerotic GVHD.
Detailed Description
A sclerotic plaque or area of skin on the right side of the body and contralaterally on the left half of the body (each maximum size: 25 cm in diameter, corresponding to the radiation field of the Hydrosun® heater 750) is selected. The assignment of one side of the body to irradiation or non-irradiation is randomized (using the MedUni Graz randomizer). The plaque randomized for irradiation is irradiated on 3 days a week for 30 minutes each time. The treatment period extends over 20 weeks, the total number of radiation treatments is therefore 60. If the patients cannot come to the radiation treatment, home therapy can be carried out according to the same treatment scheme. The radiation at the clinic is carried out with a Hydrosun® lamp 750, the home treatment with the Hydrosun® 575home (Hydrosun Medizintechnik GmbH, Mauchener Str. 14, D-79379 Muellheim, Germany). The radiation intensity at the distance of 33 cm between the device and the skin surface standardized by a distance rod is 200 mW / cm2 (visible light 50 mW / cm2, infrared A 150 mW / m2). The contralateral plaque or skin area of comparable clinical characteristics and duration of existence was included as an unirradiated control. Target and control areas will be photo-documented in the course of the study. Before the first irradiation, after the 30th and after the 60th irradiation, the skin thickness and hardness of the target and control regions are measured by a blinded examiner and the skin status including mRSS (Rodnan skin score) is recorded. In addition, at the beginning and at the end of the study, the patient's assessment of the effect (PGIC scale) and tolerability of the therapy is asked. Any side effects of the irradiation are continuously documented.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Morphea (Circumscribed Scleroderma), Sclerotic Graft-versus-host Disease (GVHD)
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
22 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Morphea
Arm Type
Other
Arm Title
Sclerotic graft-versus-host disease (GVHD)
Arm Type
Other
Intervention Type
Radiation
Intervention Name(s)
infrared-A (wIRA)
Intervention Description
Local-water filtered infrared-A (wIRA) irradiation
Primary Outcome Measure Information:
Title
Intensity of skin sclerosis
Description
as determined by a high-frequency ultrasound device with a 22 MHz applicator
Time Frame
20 weeks
Secondary Outcome Measure Information:
Title
Assessment of skin Score
Description
determined by modified Rodnan Skin Score (mRSS) (range, 0 to 51 )
Time Frame
20 weeks
Title
Assessment of skin hardness
Description
as determined by durometer
Time Frame
20 weeks
Title
Assessment of range of motions
Description
as measured by the range of motions in the presence of contractures (range, 0 to 90 degree)
Time Frame
20 weeks
Title
Grade of patient satisfaction
Description
as determined by Patients' Global Impression of Change (PGIC) scale (range, 0 to 7)
Time Frame
20 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Morphea
Sclerotic graft-versus-host disease (GVHD)
Exclusion Criteria:
Inability to cope with the treatment plan
Pregnant or breastfeeding women and women of childbearing potential without effective contraception
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Peter Wolf, MD
Phone
00 43 316 385
Ext
80315
Email
peter.wolf@medunigraz.at
First Name & Middle Initial & Last Name or Official Title & Degree
Alexandra Gruber-Wackernagel, MD
Phone
0043 316 385
Ext
13254
Email
peter.wolf@medunigraz.at
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Peter Wolf, MD
Organizational Affiliation
Medical University of Graz
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Dermatology, Medical University of Graz
City
Graz
State/Province
Styria
ZIP/Postal Code
8036
Country
Austria
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Peter Wolf, MD
Phone
031638580315
Email
peter.wolf@medunigraz.at
First Name & Middle Initial & Last Name & Degree
Alexandra Gruber-Wackernagel, MD
Phone
00 43 316 385
Ext
13254
Email
alexandra.wackernagel@medunigraz.at
First Name & Middle Initial & Last Name & Degree
Wolfgang Salmhofer, MD
First Name & Middle Initial & Last Name & Degree
Angelika Hofer, MD
First Name & Middle Initial & Last Name & Degree
Franz Legat, MD
Facility Name
Department of Dermatology, Medical University of Vienna
City
Vienna
ZIP/Postal Code
1090
Country
Austria
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Adrian Tanew, MD
Phone
+43 1 40400
Ext
77070
Email
adrian.tanew@gmail.com
First Name & Middle Initial & Last Name & Degree
Paul Jauker, MD
Phone
+43 1 40400
Ext
77070
Email
paul.jauker@meduniwien.ac.at
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Learn more about this trial
Study on the Treatment With Water-filtered Infrared-A (wIRA) Radiation in Patients With Morphea and Sclerotic Graft-versus-host Disease
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