New study aims to decode pain in kidney disease patients
NCT ID NCT06970028
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at pain in people with ADPKD, a kidney disease that often causes pain in the belly, side, and back. Researchers will use sensory tests and questionnaires to understand the pain better. They will compare results from 150 patients with those from healthy volunteers. The goal is to improve pain management and develop new treatments.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this study could help doctors better understand and manage pain in ADPKD patients, potentially leading to new pain treatments.
- What could go wrong
- This is an observational study, not a treatment trial. It will not directly improve pain for participants, and results may not lead to new therapies.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 150 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Sep 2025
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients with ADPKD from the University Hospitals Leuven will be included in this study. Additionally, healthy volunteers will be included using the registered database of the Center for Clinical Pharmacology (UZ Leuven).
- Ages
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12 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: Patients with ADPKD * Subject is ≥ 12 years old. * Subject is diagnosed with ADPKD. Healthy volunteers * Subject is ≥ 12 years old. * Subject is in good general health, based on medical history and vital signs. * Subject is matched to the patient group for age, sex and BMI. Exclusion Criteria: Patients with ADPKD * Subject has eczema, scleroderma, psoriasis, dermatitis, or any other abnormality on the skin of the dominant hand and/or lower back which, in the investigator's opinion, might interfere with the study assessments. * Subject is currently undergoing dialysis, had a kidney transplant or is a user of tolvaptan. * Female who is pregnant or breastfeeding. * Simultaneous participation in another study which, in the investigator's opinion, might confound the results of the study. * Subject is unable to refrain from drinking alcohol 24 hours prior to each study visit, and/or consumes ≥ 3 alcoholic consumptions per day. * Subject is a regular user of cannabis, any illicit drugs and/or has a history of drug abuse. * Subject is unable to refrain from drinking caffeinated beverages (such as coffee, tea, cola,…) 24 hours prior to each study visit. * Subject has used concomitant drugs and/or treatments in a period smaller than or equal to 5 half-lives prior to enrollment, that may interfere, in the investigator's opinion, with the study results. * Subject has a history of any illness or condition which, in the investigator's opinion, may interfere with safe and optimal participation in the study. Healthy volunteers * Subject has a history of any illness or condition which may affect the normal somatosensory functionality. * Subject has eczema, scleroderma, psoriasis, dermatitis, or any other abnormality on the skin of the dominant hand and/or lower back which, in the investigator's opinion, might interfere with the study assessments. * Female who is pregnant or breast-feeding. * Simultaneous participation in another study which, in the investigator's opinion, might confound the results of the study. * Subject is unable to refrain from drinking alcohol 24 hours prior to each study visit, and/or consumes ≥ 3 alcoholic consumptions per day. * Subject is a regular user of cannabis, any illicit drugs and/or has a history of drug abuse. * Subject is unable to refrain from drinking caffeinated beverages (such as coffee, tea, cola,…) 24 hours prior to each study visit. * Subject has used concomitant drugs and/or treatments in a period smaller than or equal to 5 half-lives prior to enrollment, that may interfere, in the investigator's opinion, with the study results. * Subject has a history of any illness or condition which, in the investigator's opinion, may interfere with safe and optimal participation in the study.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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UZ Leuven
RECRUITINGLeuven, 3000, Belgium
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