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Clinical Trial Details — Status: Recruiting

Administrative data

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

Study information

Verified date September 2023
Source Vejle Hospital
Contact Nina Lykkegaard Gehr, MD.
Phone +45 26618559
Email ninalykgehr@clin.au.dk
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Description:

The primary objective of the present study is to examine if a high dosage of n-3 PUFA reduces the incidence and severity of chemotherapy-induced peripheral neuropathy (CIPN) 8 months after adjuvant oxaliplatin following surgery for high-risk colorectal cancer. An additional aim is to investigate whether n-3 PUFAs have an effect on nutritional status, cognition and mental status. Inflammatory mechanisms and biomarkers of CIPN in skin biopsies and in blood will be explored.


Recruitment information / eligibility

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

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Fish oil
Fish oil containing poly unsaturated fatty acids.
Corn oil
Corn oil

Locations

Country Name City State
Denmark Deparment of Oncology, Vejle Hospital Vejle

Sponsors (1)

Lead Sponsor Collaborator
Vejle Hospital

Country where clinical trial is conducted

Denmark, 

Outcome

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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