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Clinical Trial Details

Trial ID: L0357
Source ID: NCT05750875
Associated Drug: Loratadine
Title: Gabapentin Versus Loratadine in Uremic Pruritus
Acronym:
Status: COMPLETED
Study Results: NO
Results:
Conditions: Pruritus|Uremia|Chronic Kidney Diseases
Interventions: DRUG: Loratadine|DRUG: Gabapentin
Outcome Measures: Primary: Mean reduction in pruritus score, from baseline till 4 weeks, as measured on a numerical rating scale., Reduction in pruritus score as measured on a numerical rating scale, numbered between '0' (corresponding to no itch) and '10' (the worst imaginable itch)., Four weeks | Secondary: Mean reduction in Dermatology Life Quality Index Questionnaire score, from baseline till 4 weeks., Dermatology Life Quality Index Questionnaire score ranging from from 0 (no impairment of life quality) to 30 (maximum impairment)., Four weeks|Comparison of side effects of gabapentin and loratadine, as reported by the participants., Four weeks
Sponsor/Collaborators: Sponsor: King Edward Medical University
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases: PHASE4
Enrollment: 64
Study Type: INTERVENTIONAL
Study Designs: Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: NONE|Primary Purpose: TREATMENT
Start Date: 2022-05-01
Completion Date: 2022-10-31
Results First Posted:
Last Update Posted: 2023-03-16
Locations: King Edward Medical University/Mayo Hospital, Lahore, Punjab, 54000, Pakistan
URL: https://clinicaltrials.gov/show/NCT05750875