CKD (Chronic Kidney Disease) Stage 5D

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Review clinical trials related to CKD (Chronic Kidney Disease) Stage 5D. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Effect of Canagliflozin on Ultrafiltration & Fibrosis in Patients on Peritoneal Dialysis

This is a phase II, proof-of-concept, placebo-controlled, double-blind, cross-over randomized clinical trial, assessing the effect of canagliflozin on peritoneal membrane function in patients on PD. The primary aim of this trial is to determine the short-term effects of canagliflozin, an SGLT-2 inhibitor, on glucose absorption by the peritoneal membrane and on ultrafiltration, as assessed by a standardized peritoneal equilibrium test. The secondary aims are to determine the effect of canagliflozin on solute clearance and on effluent biomarkers of inflammation, angiogenesis, and fibrosis at 26 weeks. We hypothesize that canagliflozin will prevent glucose absorption by the peritoneal membrane, as compared with placebo, and will attenuate the development of inflammation, angiogenesis, and fibrosis of the peritoneal membrane, as assessed by relevant biomarkers in the dialysate.

Participants needed: 30
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: McGill University Health Centre/Research Institute of the McGill University Health CentreUpdated: Mar 16, 2026Locations: 1
Eligibility criteria

Adult patients with kidney failure on PD (both incident and prevalent) who are o... [+1]

History of euglycemic ketoacidosis [+7]

Status: Not yet recruiting

Tubeless Spontaneous Ventilation Anesthesia in Kidney Transplantation

The aim of this clinical trial is to compare the intraoperative use of neuromuscular blocking agents and other anesthetic drugs between tubeless spontaneous ventilation anesthesia (TSVA) and conventional endotracheal intubation (ETT) anesthesia in kidney transplantation. The study will also evaluate the safety, stability, and postoperative recovery associated with TSVA. This trial is designed to address the following questions: * Does TSVA reduce the intraoperative requirement for neuromuscular blocking agents and other anesthetic medications? * Does TSVA improve postoperative outcomes in kidney transplant recipients? * How do the intraoperative safety and stability of TSVA compare with those of ETT anesthesia? Researchers will compare anesthetic drug consumption, intraoperative anesthetic performance, and postoperative recovery outcomes between the TSVA and ETT groups to determine whether TSVA can decrease anesthetic drug use and enhance patient recovery. Participants will: * Undergo a complete preoperative assessment * Receive kidney transplantation under TSVA or ETT anesthesia, with relevant intraoperative data recorded * Receive tubeless postoperative management, with documentation of pain scores, complications, and recovery of graft function * Be followed throughout their lifetime after discharge, providing long-term follow-up information

Participants needed: 60
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Jianxing HeUpdated: Jan 29, 2026
Eligibility criteria

No gender restriction, age 18-65 years (including upper and lower limits). [+9]

Combined multi-organ transplantation. [+6]

Status: Recruiting

Studies on Adsorption International Learning Initiative Global

Use of sorption technologies in patients undergoing maintenance hemodialysis with inflammatory syndrome and clinical manifestations of uremia

Participants needed: 60
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Botkin HospitalUpdated: Dec 10, 2025Locations: 1
Eligibility criteria

Adequate dialysis defined by a KT/V index ≥ 1.4 [+4]

Current use of steroids or immunosuppressive therapy [+3]

Status: Recruiting

ASPIrin in Reducing Events in Dialysis ( ASPIRED )

People with kidney failure requiring dialysis have a much higher risk of developing cardiovascular (CV) disease compared with the general population. A cardiac cause accounts for 58% of all deaths in patients with end stage kidney disease (ESKD). At the same time, this population has increased risks of clotting as well as bleeding episodes. While aspirin is known to reduce cardiovascular complications in the general population, evidence to support the use of aspirin in people with ESKD receiving dialysis therapy is currently lacking. The ASPIrin to Reduce Event in Dialysis (ASPIRED) trial will test whether aspirin use in dialysis patients safely improves outcomes compared with no aspirin use.

Participants needed: 9,000
Trial details
Phase: Phase 4Age: 18+Biological sex: AllType: InterventionalSponsor: Guangdong Provincial People's HospitalUpdated: Nov 18, 2025Locations: 139
Eligibility criteria

Incident or prevalent adults (≥18 years old) dialysis patients are included in t... [+2]

Requirement for any form of antiplatelet agent (aspirin, glycoprotein IIb/IIIa i... [+5]

Status: Recruiting

Effect of Kidney Replacement Therapy with Polymethylmethacrylate Membranes on Pruritus-related Quality of Life in Patients Receiving Maintenance Haemodialysis

This randomized controlled trial aims to evaluate the effect of polymethylmethacrylate dialysis membranes use on the intensity of pruritus in patients with CKD stage 5D receiving maintenance hemodialysis. The main question it aims to answer is: Does the use of polymethylmethacrylate (PMMA) membranes reduce the intensity of pruritus in dialysis patients? Researchers will compare PMMA membranes to standard polysulfone-based membranes to see if PMMA works to reduce moderate-to-severe pruritis and pruritis-related quality of life. Participants will: * receive maintenance hemodialysis with PMMA or polysulfone membranes for 2 months; * fill in questionnaires about intensity of pruritis and its impact on daily life.

Participants needed: 62
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Saint Petersburg State University, RussiaUpdated: Mar 4, 2025Locations: 1
Eligibility criteria

Diagnosis of CKD stage 5D, maintenance hemodialysis not less than 3 months prior... [+4]

Presence of active skin disease, cholestasis, severe secondary hyperparathyroidi... [+2]

Status: Recruiting

Impact of Propionic Acid on Regulatory T Cell Function in Children With CKD

Pro-Kids is a multi-center, double-blind, randomized and placebo-controlled intervention study in children with chronic kidney disease. The investigators address the effect of a dietary food supplementation of propionic acid on the immune system and the function of the intestinal barrier in CKD patients treated with hemodialysis.

Participants needed: 16
Trial details
Age: 12-20Biological sex: AllType: InterventionalSponsor: Charite University, Berlin, GermanyUpdated: Feb 18, 2025Locations: 1
Eligibility criteria

Body weight: > 30kg [+4]

Disease or dysfunctions, which disqualifies the patient [+10]

Status: Recruiting

Genetics in the Progression of Nephropathies

This study evaluates the role of genetic in the development and progression of different nephropaties with particular attention to: * AKI * CKD * Hypertension * ADPKD * CKD-MBD * Patients with decompensated heart failure undergoing either medical or surgery therapy * Patients with hematologic cancer exposed to chemotherapeutic agents or undergoing allogeneic bone marrow transplantation * glomerular diseases

Participants needed: 10,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Ospedale San RaffaeleUpdated: May 16, 2024Locations: 1
Eligibility criteria

to be evaluated in the different sub-protocols