Skip to content

PHOTOTHERAPY VERSUS PREGABALIN IN TREATMENT OF REFRACTORY UREAMIC PRURITIS

NARROW BAND UVB PHOTOTHERAPY VERSUS PREGABALIN IN TREATMENT OF REFRACTORY PRURITIS IN END STAGE RENAL DISEASE PATIENTS

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04660773
Enrollment
40
Registered
2020-12-09
Start date
2021-08-01
Completion date
2022-03-01
Last updated
2021-07-26

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

Conditions

Refractory Uremic Pruritis

Brief summary

Patients will be randomly assigned into 2 groups: 1. Group A: (20 patients) will receive NB UVB phototherapy 3 sessions per week for 2 months. 2. Group B: (20 patients) will receive pregabalin oral therapy (50mg after each dialysis session) for 2 months.

Interventions

ultraviolet phototherapy sessions

DRUGPregabalin

oral medication

Sponsors

Alexandria University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

1. Age: 20-60 years. 2. 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). 3. Refractory uremic pruritis.

Exclusion criteria

1. Other causes of pruritis (Dermatological or systemic) e.g. atopic, cholestatic liver disease. 2. Photosensitivity. 3. Contraindication or allergy to pregabalin. 4. Patients on antipruritic drugs e.g. antihistamines, steroids, emollients, opioid agonists.

Design outcomes

Primary

MeasureTime frameDescription
5 D-itching scaletwo monthassessment of degree, duration, direction, disability and distribution of itching

Countries

Egypt

Contacts

Primary Contactmarwa eldeeb
marwa.eldeeb16@alexmed.edu.eg01200029774

Outcome results

None listed

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