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International CIPN Assessment and Validation Study
RecruitingObservational study
International Chemotherapy Induced Peripheral Neurotoxicity (CIPN) Assessment and Validation Study
Who can join
Ages 18 and older · All sexes
Full eligibility criteria
Inclusion Criteria Subjects must meet all of the following inclusion criteria to be eligible for enrolment into the study: 1. Subjects must be candidates for neurotoxic chemotherapy at doses expected to be potentially neurotoxic (a list of neurotoxic drugs is provided in Appendix 1). 2. Male and female subjects who are 18 years of age or older. 3. Subjects freely provide informed consent by signing and dating an informed consent form prior to study entry. 4. Subjects must be willing to complete all study-related activities and follow-up visits required by the protocol. 5. Subjects must have a Karnofsky performance score greater than or equal to 70. Exclusion Criteria Subjects presenting with any of the following will not be included in the study: 1. Poor prognosis, with high probability to be unable to complete the planned chemotherapy treatment. 2. Concomitant neurologic conditions (e.g., brain tumor, spinal or brain metastases) that would interfere or complicate the assessments. 3. Severe depression that in the opinion of the Investigator would complicate the assessments. 4. Chronic treatment with antiepileptic drugs, antidepressants and major analgesics, unless stable dosing and conditions have been reached for 3 months prior to entry. 5. Preventive interventions (e.g., antioxidants, cryotherapy, distal pressure). 6. Subjects who are currently receiving another medication other than antineoplastic chemotherapy drugs that has known potential to produce neurologic peripheral nerve toxicity (e.g. metronidazole, isoniazid, amiodarone, antiretroviral medications). 7. Subjects with any other condition, which, in the investigator's judgment, might decrease the chance of obtaining satisfactory data to achieve the objectives of the study. 8. Previous neurotoxic chemotherapy.
About the 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 being tested
- outcome measures for CIPN testing (other)
Sponsor: University of Milano Bicocca · Participants: 1,000 · Started: Jun 8, 2020
Contact the study team
- GUIDO CAVALETTI, MD · Phone: + 39 02 6448 8039
- PAOLA ALBERTI, MD, PhD · Phone: +39 02 6448 8154
Official record on ClinicalTrials.gov — NCT04633655
Locations in the U.S.
| Alabama | Birmingham School of Nursing, University of Alabama, Birmingham (Not yet recruiting) |
| Georgia | Northside Hospital, Atlanta (Not yet recruiting) |
| Maryland | JHU, Baltimore (Not yet recruiting) |
| Michigan | University of Michigan School of Nursing, Ann Arbor (Not yet recruiting) |
| New York | Columbia University Irving Medical Center, New York (Not yet recruiting) |
| Ohio | Cancer Center/Wexner Medical Center - Ohio State Medical Oncology Division, Columbus (Not yet recruiting) |
| Pennsylvania | Dartmouth-Hitchcock Medical Center, Lebanon (Not yet recruiting) |
| Vermont | University of Vermont Medical Center, Burlington (Not yet recruiting) |
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.