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CKD-aP Among Adults on Dialysis in Switzerland

Uremic Pruritus Among Adults on Dialysis in the French Speaking Part of Switzerland

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05415969
Acronym
UP-RAISE
Enrollment
401
Registered
2022-06-13
Start date
2022-09-01
Completion date
2023-10-09
Last updated
2023-11-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Kidney Diseases, Chronic Kidney Diseases Associated Pruritus, Dialysis

Keywords

Chronic Kidney Disease; Dialysis; Pruritus

Brief summary

Chronic Kidney Disease Associated Pruritus (CKD-aP) represents a localized or a generalized skin itch, which is a common symptom occurring in end-stage renal disease and dialysis. The prevalence of CKD-aP in adults on dialysis varies between countries ranging between 20-42%. Swiss data on CKD-aP are unfortunately largely lacking, as Switzerland is so far not part of large registries, such as DOPPS. The aging population, the increase in diabetes (69% by 2030), the increase in hypertension (60% by 2025) and poly-morbidity will probably lead to a rise in the number of patients on dialysis and subsequent CKD-aP. CKD-aP is associated with sleep disturbances, compromised quality of life, emotional distress, and increased risks of hospitalization and death. Its management lacks approaches that are supported by strong evidence because its pathogenesis remains poorly understood and may be related to an increase in uremic toxins, skin inflammation. In this context, sweat composition deserves more attention. Aim of the study The aim of the study is to determine the prevalence of CKD-aP in the population on dialysis, the association between CKD-aP and different electrolytes, and the potential role of the composition of sweat in CKD-aP. Results will be used for building a CKD-aP symptom management program to improve the quality of care of patients on dialysis and will be incorporated in the nursing continuing education program.

Interventions

OTHERCKD-aP

Identification of CKD-aP prevalence and severity among patients on dialysis.

Sponsors

University of Lausanne Hospitals
CollaboratorOTHER
Hôpital Fribourgeois
CollaboratorOTHER
University Hospital, Geneva
CollaboratorOTHER
Valais Hospital
CollaboratorUNKNOWN
eHnv Hospital
CollaboratorUNKNOWN
Rennaz Hospital
CollaboratorUNKNOWN
Intercantonal Hospital of Broye
CollaboratorUNKNOWN
GHOL Nyon Hospital
CollaboratorUNKNOWN
Dialyse Riviera
CollaboratorUNKNOWN
Cecil Clinic Hirslanden Private Hospital Group
CollaboratorUNKNOWN
Vifor Pharma
CollaboratorINDUSTRY
Réseau Hospitalier Neuchâtelois
CollaboratorOTHER
University of Applied Sciences of Western Switzerland
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adult ≥ 18 years old * Diagnosed with end-stage renal disease and receiving hemodialysis for at least 6 months * Able to communicate in French or availability of a French-speaking close relative for translation * Signed informed consent Additional inclusion criteria for the case-control study outcomes phase 2: * Reporting moderate to severe CKD-aP for the participant considered as a case * Reporting no or mild CKD-aP for the participant considered as a control Cases and controls will be matched by age-group, sex, and dialysis modality (hemodialysis or peritoneal dialysis).

Exclusion criteria

* Presence of cognitive impairment or cognitive disorder

Design outcomes

Primary

MeasureTime frameDescription
Prevalence of CKD-aPJune 27, 2022- October 31, 2023Evaluation of the presence of CKD-aP. This outcome prevalence will be reported in %.
Severity of CKD-aP using the Visual Analog ScaleJune 27, 2022- October 31, 2023Severity of CKD-aP will be measured using the Visual Analog Scale (VAS) questionnaire. Participants will be asked to rate their maximum pruritus intensity during the last 24 hours. The VAS score ranges from 0 (not itchy) to 10 (extremely itchy); Severity will be classified into five categories: 1) 0 = no pruritus, 2) 0.1-2.9 points = mild pruritus, 3) 3.0-6.9 points = moderate pruritus, 4) 7.0-8.9 points = severe pruritus, and 5) 9.0-10.0 points = very severe pruritus. Higher scores indicate a worse outcome.
Severity of CKD-aP using the Verbal Rating ScaleJune 27, 2022- October 31, 2023Severity of CKD-aP will also be measured using the Verbal Rating Scale (VRS) questionnaire. Participants will be asked to rate their maximum pruritus intensity during the last 24 hours. The VRS is a five-point scale and consists of a list of adjectives describing various levels of symptom intensity (0= no itch, 1= mild itch, 2= moderate itch, 3= severe itch and 4=very severe itch). Higher scores indicate a worse outcome.

Secondary

MeasureTime frameDescription
Calcium level (mg/l) in sweatJune 27, 2022- October 31, 2023Measurement of calcium (mg/l) in a subgroup of patients with CKD-aP and their age-sex-matched controls on dialysis. 60 participants (30 cases and 30 controls)
Sodium level (mmol/l) in sweatJune 27, 2022- October 31, 2023Measurement of sodium (mmol/l) in a subgroup of patients with CKD-aP and their age-sex-matched controls on dialysis. 60 participants (30 cases and 30 controls)
Urea level (mmol/l) in sweatJune 27, 2022- October 31, 2023Measurement of urea (mmol/l) in a subgroup of patients with CKD-aP and their age-sex-matched controls on dialysis. 60 participants (30 cases and 30 controls)
Phosphorus level (mg/ml) in sweatJune 27, 2022- October 31, 2023Measurement of phosphorus (mg/ml) in a subgroup of patients with CKD-aP and their age-sex-matched controls on dialysis. 60 participants (30 cases and 30 controls)
Chloride level (mmol/l) in sweatJune 27, 2022- October 31, 2023Measurement of chloride (mmol/l) in a subgroup of patients with CKD-aP and their age-sex-matched controls on dialysis. 60 participants (30 cases and 30 controls)
Potassium level (mmol/l) in sweatJune 27, 2022- October 31, 2023Measurement of potassium (mmol/l) in a subgroup of patients with CKD-aP and their age-sex-matched controls on dialysis. 60 participants (30 cases and 30 controls)

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026