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Randomized Study Evaluating Safety of Short Hydration Method for Cisplatin Administration Compared With Conventional Hydration
The aim of the study is to evaluate safety of short hydration with cisplatin administration. The main outcome is renal dysfunction following cisplatin use with short hydration protocol. Another group of patients received conventional hydration is the historical control for comparison (Randomized phase II design with a reference standard treatment control arm)
Age
18 - 75 years
Sex
ALL
Healthy Volunteers
No
Faculty of Medicine Siriraj Hospital
Bangkok, Thailand
Start Date
March 7, 2023
Primary Completion Date
January 7, 2025
Completion Date
March 7, 2025
Last Updated
June 1, 2023
100
ESTIMATED participants
short hydration
PROCEDURE
conventional hydration
PROCEDURE
Lead Sponsor
Mahidol University
Collaborators
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT02769975