Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID07413315

Benefits of a Renal Rehabilitation Program Adapted to Uremic Patients on Daily Hemodialysis at Low Dialysate Flow Rate

Led by Brugmann University Hospital · Updated on 2026-02-17

50

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating a renal rehabilitation program tailored for patients with terminal chronic kidney disease (CKD) who require hemodialysis. The study focuses on patients recently hospitalized due to acute medical events. It aims to explore the benefits of daily low dialysate flow rate hemodialysis (LDF), a newer dialysis method, in combination with rehabilitation, to address common issues like sarcopenia and decreased physical function associated with CKD and conventional hemodialysis. The study involves patients undergoing low flow rate hemodialysis five times per week along with a customized multidisciplinary rehabilitation program. This approach is compared to conventional hemodialysis, aiming to maintain dialysis efficiency while allowing better cardiovascular tolerance and physical recovery. The rehabilitation program and dialysis treatments are integrated during the patient's stay in a rehabilitation ward, which can last up to 24 weeks. Participants will be assessed through various tests at admission and discharge from the rehabilitation ward, including hand grip strength, physical performance, walking ability, muscle ultrasound, and quality of life surveys. Blood tests measuring myostatin, activin A, and IGF1 levels will also be conducted. The study monitors dialysis adequacy and the patient's response to the rehabilitation program, tracking progress over the rehabilitation period to evaluate improvements in muscle strength and overall physical condition.

CONDITIONS

Brief Title

Benefits of a Renal Rehabilitation Program Adapted to Uremic Patients on Daily Hemodialysis at Low Dialysate Flow Rate.

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient with terminal chronic kidney disease requiring hemodialysis treatment
  • Patient recently hospitalized for an acute medical event
Not Eligible

You will not qualify if you...

  • Dementia or mild cognitive impairment with MMSE score below 20/30
  • Decompensated psychiatric disorder or behavioral issues
  • Pregnant woman
  • Recovery of kidney function allowing stopping hemodialysis
  • Candidate for neurological rehabilitation
  • Recent spinal cord injury
  • Absolute or relative contraindication to stress test
  • Severe or poorly tolerated cardiac rhythm disorder
  • Severe or symptomatic obstruction to left ventricular ejection
  • Decompensated heart failure
  • Acute myocarditis, pericarditis, or endocarditis
  • Acute aortic dissection
  • High-risk emboligenic intracardiac thrombus
  • Significant stenosis of the common trunk
  • Ventricular aneurysm
  • Supraventricular tachycardia with poorly controlled ventricular rate, acquired high-degree or complete block
  • Obstructive cardiomyopathy with high resting gradient
  • Recent stroke or transient ischemic attack
  • Acute venous thrombosis with or without pulmonary embolism
  • Poorly controlled clinical condition such as severe anemia, significant electrolyte imbalance, or hyperthyroidism
  • Lack of cooperation from the patient
  • Blood pressure above 200/110 mmHg

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - Up to 24 weeks

Participants receive low flow rate hemodialysis five times per week along with a tailor made multidisciplinary rehabilitation program.

Regular visits during rehabilitation program

Trial Site Locations

Total: 1 location

1

CHU Brugmann

Brussels, Belgium, 1020

Actively Recruiting

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Research Team

J

Joris Vanparys, MD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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