Colorectal Cancer Clinical Trial
— OxaNeuroOfficial title:
Prevention of Oxaliplatin-induced Peripheral Neuropathy - a Randomized Controlled Trial
NCT number | NCT05404230 |
Other study ID # | OxaNeuro |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | July 15, 2022 |
Est. completion date | December 2026 |
The purpose of this study is to examine the effect of supplementary polyunsaturated fatty acids on nerve damage in the body's extremitites of patients treated with oxaliplatin containing chemotherapy after surgery for colorectal cancer.
Status | Recruiting |
Enrollment | 120 |
Est. completion date | December 2026 |
Est. primary completion date | December 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Histopathologically verified adenocarcinoma of the colon or rectum and planned standard adjuvant treatment with capecitabine in combination with oxaliplatin. - ECOG performance status 0-2 (measurement of a patient's function in terms of self-care, daily activity and physical ability. - Written and orally informed informed consent Exclusion Criteria: - Inability to speak, read, and understand Danish. - Previous treatment with neurotoxic chemotherapy. - Neurological (including neuropathy) or psychiatric disorders, diabetes or other significant medical conditions. - Alcohol or drug abuse. - Sensory disturbances in the feet - Spinal stenosis. - Vascular disease (Fontaine grade II or more). - Known allergy to fish, fish oil or corn oil - Fertile patients not willing to use effective methods of contraception during treatment or abstinence. - Daily intake of oil supplements and not willing to stop during the trial period. - Lack of consent to skin biopsy |
Country | Name | City | State |
---|---|---|---|
Denmark | Deparment of Oncology, Vejle Hospital | Vejle |
Lead Sponsor | Collaborator |
---|---|
Vejle Hospital |
Denmark,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Incidence of chemotherapy induced peripheral neuropathy (CIPN) 8 months after start of adjuvant chemotherapy | Number of patients who meet the criteria for CIPN: relevant symptoms evaluated by a medical doctor, incl one of the following: abnormal vibration test or, abnormal nerve conduction test by DPN check device or, abnormal pinprick test or, abnormal skin biopsy. | 8 months after start of adjuvant chemotherapy | |
Secondary | Intensity of CIPN-related neuropathic pain 8 months after adjuvant chemotherapy according to the Numeric Rating Scale (NRS) | Average over the past 24 hours measured by NRS (scale from 0-10 with 0=no pain and 10=worst pain imaginable) | 8 months after start of adjuvant chemotherapy | |
Secondary | Change in severity of CIPN from baseline to 8 months after start of adjuvant chemotherapy according to the EORCT QLQ-CIPN 20 questionnaire | EORCT QLQ-CIPN 20 = the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire-Chemotherapy Induced Peripheral Neuropathy | 8 months after start of adjuvant chemotherapy |
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