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Clinical Trial Details

Trial ID: L1211
Source ID: NCT00745199
Associated Drug: Cromolyn Sodium
Title: Evaluating the Effect of Cromolyn Sodium in Uremic Pruritus
Acronym:
Status: COMPLETED
Study Results: NO
Results:
Conditions: End Stage Renal Disease|Pruritus
Interventions: DRUG: cromolyn sodium|DRUG: placebo
Outcome Measures: Primary: pruritus, 3 months | Secondary: serum tryptase level, 4 months
Sponsor/Collaborators: Sponsor: Shiraz University of Medical Sciences
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases: PHASE2
Enrollment: 62
Study Type: INTERVENTIONAL
Study Designs: Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: DOUBLE (PARTICIPANT, INVESTIGATOR)|Primary Purpose: TREATMENT
Start Date: 2008-05
Completion Date: 2009-06
Results First Posted:
Last Update Posted: 2009-08-18
Locations: Shiraz University of Medical sciences, Nemazi and Faghihi Hospital, Shiraz, Fars, 71345, Iran, Islamic Republic of
URL: https://clinicaltrials.gov/show/NCT00745199