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NCT05780086

Safety of and Tolerability to a Sodium-free Peritoneal Dialysis Solution

Status unknown Phase 1 Last updated 28 March 2023
What this trial tests

Phase 1 trial testing 30% icodextrin and 10% dextrose in Chronic Kidney Diseases in 10 participants. Status unknown.

Timeline
3 February 2023
Primary endpoint
30 August 2023
30 December 2023

Quick facts

Lead sponsorInstituto Mexicano del Seguro Social
PhasePhase 1
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment10
Start date3 February 2023
Primary completion30 August 2023
Estimated completion30 December 2023
Sites1 location across Mexico

Drugs / interventions tested

Conditions studied

Sponsor

Instituto Mexicano del Seguro Social — full company profile →

Who can join

18 and older, any sex, with Chronic Kidney Diseases. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study will evaluate the safety and tolerability profile of a dwell time (bath) of 24 hours using a 500 ml sodium-free peritoneal dialysis solution based on 30% icodextrin and 10% dextrose in patients with chronic kidney failure undergoing peritoneal dialysis

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Development of a Novel Intraperitoneal Icodextrin/Dextrose Solution for Enhanced Sodium Removal.
    Asher JL, Ivey-Miranda JB, Maulion C, Cox ZL, et al · · 2025 · cited 4× · PMID 39790231 · DOI 10.1016/j.xkme.2024.100938

Verify or expand the search:

Other recruiting trials for Chronic Kidney Diseases

Currently open trials in the same condition.

Other Instituto Mexicano del Seguro Social trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05780086.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing