Tokyo, April 22 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000061335) titled 'Changes in solute removal performance due to changes in dialysate flow rate settings' on April 21.
Study Type:
Interventional
Study Design:
Basic Design - Single arm
Randomization - Non-randomized
Blinding - Open -no one is blinded
Control - Uncontrolled
Primary Sponsor:
Institute - Kawashima Hospital
Condition:
Condition - Patients with end-stage renal failure exhibiting malnutrition with serum albumin levels below 3.0 g/dl.
Classification by malignancy - Others
Genomic information - NO
Objective:
Narrative objectives1 - To investigate the conditions for dialysis treatment according to the pathological condition of patients with end-stage renal failure.
Basic objectives2 - Efficacy
Intervention:
Interventions/Control_1 - Dialysis fluid volume change intervention
Eligibility:
Age-lower limit - 20
years-old
<=
Age-upper limit - Not applicable
Gender - Male and Female
Key inclusion criteria - 1. Patients exhibiting malnutrition with serum albumin levels below 3.0 g/dl
2. Patients who can maintain a stable blood flow rate of 250 ml/min or more during treatment
Key exclusion criteria - 1. Patients who are deemed inappropriate by the principal investigator
2. Patients who cannot provide written informed consent
Target Size - 6
Recruitment Status:
Recruitment status - Preinitiation
Date of protocol fixation - 2026 Year 04 Month 10 Day
Date of IRB - 2026 Year 04 Month 20 Day
Anticipated trial start date - 2026 Year 04 Month 21 Day
Last follow-up date - 2026 Year 12 Month 31 Day
To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000070131
Disclaimer: Curated by HT Syndication.
