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International CIPN Assessment and Validation Study
NCT04633655 · View on ClinicalTrials.gov ↗
Study Summary
This is an observational study of chemotherapy-induced peripheral neurotoxicity (CIPN) patients to be investigated prospectively in order to assess responsiveness of a set of outcome measures in an international multi-center study.
Conditions Studied
Interventions
- OTHER outcome measures for CIPN testing
Study Locations (20)
Other
- Brain and Mind Center — Sydney
- Dept. of Neurology, Medical University of Vienna — Vienna
- International Centre for Diarrhoeal Disease Research — Dhaka
- Clínica AMO — Salvador
- The Ottawa Hospital — Ottawa
- Aarhus University Hospital — Aarhus
- Hôpital Percy — Clamart
- CHU Dupuytren — Limoges
- Center for Molecular Medicine — Cologne
- University of Larissa — Larissa
- "Saint Andrew's" State General Hospital — Pátrai
Alabama
- Birmingham School of Nursing, University of Alabama — Birmingham
Georgia
- Northside Hospital — Atlanta
Maryland
- JHU — Baltimore
Michigan
- University of Michigan School of Nursing — Ann Arbor
New York
- Columbia University Irving Medical Center — New York
Ohio
- Cancer Center/Wexner Medical Center - Ohio State Medical Oncology Division — Columbus
Pennsylvania
- Dartmouth-Hitchcock Medical Center — Lebanon
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,000 participants |
| Start Date | 2020-06-08 |
| Est. Completion | 2025-12-31 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04633655
The ClinicalTrials.gov registry entry for NCT04633655 describes a study currently listed as recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 1,000 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Milano Bicocca, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 2 conditions, with Quality of Life appearing as the primary indexed condition, and to 1 intervention — of which outcome measures for CIPN testing is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT04633655 reports 20 study locations spanning 10 distinct geographic areas — top geographies include Other, Alabama, Georgia. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT04633655 about?
NCT04633655 is a clinical study titled "International CIPN Assessment and Validation Study". This is an observational study of chemotherapy-induced peripheral neurotoxicity (CIPN) patients to be investigated prospectively in order to assess responsiveness of a set of outcome measures in an international multi-center study.
What is the current status of trial NCT04633655?
This trial is currently recruiting. The enrollment target is 1,000 participants. The study started on 2020-06-08. Estimated completion is 2025-12-31.
What conditions does trial NCT04633655 study?
This clinical trial studies the following conditions: Quality of Life, Chemotherapy-induced Peripheral Neuropathy. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT04633655?
The interventions under investigation include: outcome measures for CIPN testing (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT04633655?
This trial is sponsored by University of Milano Bicocca, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT04633655 being conducted?
This trial has 20 study locations across Alabama, Georgia, Maryland, Michigan, New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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