Hemodialysis Clinical Trial
Official title:
A Prospective Randomized, Double-Blind Parallel Group Trial To Assess The Efficacy And Safety Of Intravenous Dextrose 5% Solution Compare With Normal Saline (Standard Care) In Rinsing During Haemodialysis In Subjects With End Stage Renal Failure (ESRF) With Respect To Systolic Blood Pressure Control Over 3 Months Period.
This is a prospective, randomized, double-blind, parallel group trial to assess the efficacy
and safety of intravenous dextrose 5% solution compare with normal saline (standard care) in
wash back procedure during haemodialysis in patients with end stage renal failure (ESRF)
with respect to systolic blood pressure control over 3 months period.
The primary objective is to establish efficacy of 5% dextrose solution compared with normal
saline (0.9% sodium chloride solution) with respect to systolic blood pressure control in
subjects with end stage renal failure (ESRF) on regular hemodialysis. Secondary objectives
include monitoring the change in body weight, thirst level and body fluid volume.
n/a
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator)
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