PHOTOTHERAPY VERSUS PREGABALIN IN TREATMENT OF REFRACTORY UREAMIC PRURITIS
Primary Purpose
Refractory Uremic Pruritis
Status
Unknown status
Phase
Phase 2
Locations
Egypt
Study Type
Interventional
Intervention
NB UVB phototherapy
Pregabalin
Sponsored by
About this trial
This is an interventional treatment trial for Refractory Uremic Pruritis
Eligibility Criteria
Inclusion Criteria:
- Age: 20-60 years.
- End stage renal disease (the last stage(stage 5) of chronic disease which means kidneys are only functioning at 10 to 15 percent of their normal capacity and dialysis or kidney transplant is necessary to stay alive).
- Refractory uremic pruritis.
Exclusion Criteria:
- Other causes of pruritis (Dermatological or systemic) e.g. atopic, cholestatic liver disease.
- Photosensitivity.
- Contraindication or allergy to pregabalin.
- Patients on antipruritic drugs e.g. antihistamines, steroids, emollients, opioid agonists.
Sites / Locations
- Faculty of MedicineRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
NB UVB phototherapy
pregabalin
Arm Description
(20 patients) will receive NB UVB phototherapy 3 sessions per week for 2 months.
20 patients) will receive pregabalin oral therapy (50mg after each dialysis session) for 2 months.
Outcomes
Primary Outcome Measures
5 D-itching scale
assessment of degree, duration, direction, disability and distribution of itching
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04660773
Brief Title
PHOTOTHERAPY VERSUS PREGABALIN IN TREATMENT OF REFRACTORY UREAMIC PRURITIS
Official Title
NARROW BAND UVB PHOTOTHERAPY VERSUS PREGABALIN IN TREATMENT OF REFRACTORY PRURITIS IN END STAGE RENAL DISEASE PATIENTS
Study Type
Interventional
2. Study Status
Record Verification Date
July 2021
Overall Recruitment Status
Unknown status
Study Start Date
August 1, 2021 (Anticipated)
Primary Completion Date
March 1, 2022 (Anticipated)
Study Completion Date
March 1, 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Alexandria University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
Yes
5. Study Description
Brief Summary
Patients will be randomly assigned into 2 groups:
Group A: (20 patients) will receive NB UVB phototherapy 3 sessions per week for 2 months.
Group B: (20 patients) will receive pregabalin oral therapy (50mg after each dialysis session) for 2 months.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Refractory Uremic Pruritis
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
40 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
NB UVB phototherapy
Arm Type
Active Comparator
Arm Description
(20 patients) will receive NB UVB phototherapy 3 sessions per week for 2 months.
Arm Title
pregabalin
Arm Type
Active Comparator
Arm Description
20 patients) will receive pregabalin oral therapy (50mg after each dialysis session) for 2 months.
Intervention Type
Device
Intervention Name(s)
NB UVB phototherapy
Intervention Description
ultraviolet phototherapy sessions
Intervention Type
Drug
Intervention Name(s)
Pregabalin
Intervention Description
oral medication
Primary Outcome Measure Information:
Title
5 D-itching scale
Description
assessment of degree, duration, direction, disability and distribution of itching
Time Frame
two month
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age: 20-60 years.
End stage renal disease (the last stage(stage 5) of chronic disease which means kidneys are only functioning at 10 to 15 percent of their normal capacity and dialysis or kidney transplant is necessary to stay alive).
Refractory uremic pruritis.
Exclusion Criteria:
Other causes of pruritis (Dermatological or systemic) e.g. atopic, cholestatic liver disease.
Photosensitivity.
Contraindication or allergy to pregabalin.
Patients on antipruritic drugs e.g. antihistamines, steroids, emollients, opioid agonists.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
marwa eldeeb
Phone
01200029774
Email
marwa.eldeeb16@alexmed.edu.eg
Facility Information:
Facility Name
Faculty of Medicine
City
Alexandria
ZIP/Postal Code
21521
Country
Egypt
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
alexandria university faculty of medicine
Phone
034862506
Email
alexmed@edu.eg
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
PHOTOTHERAPY VERSUS PREGABALIN IN TREATMENT OF REFRACTORY UREAMIC PRURITIS
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