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Tests magnesium for nerve symptoms and sleep in colorectal cancer chemotherapy

Tests magnesium supplements in adults with colorectal cancer receiving chemotherapy.

Plain-language title generated from the registry record
Registry title: Exploring the Effects of Magnesium Ions on Peripheral Neuropathy, Serum Magnesium Ion Concentration,Sleep Quality, and Quality of Life in Patients With Colorectal Cancer Receiving Chemotherapy.

Key facts

Where
Kaohsiung City, TaiwanSee the site

Where in Taiwan

  • Kaohsiung Medical University Chung-Ho Memorial HospitalKaohsiung City, TaiwanNo longer taking part

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Trial details

Who runs it
Kaohsiung Medical University Chung-Ho Memorial Hospital
Trial code
NCT07346469
Record updated
16 January 2026
Original description
Chemotherapy for colorectal cancer (CRC) is frequently complicated by chemotherapy-induced peripheral neuropathy (CIPN) and impaired sleep quality, significantly impacting patient quality of life. Low magnesium levels have been implicated in peripheral nerve dysfunction. This interventional study aims to investigate the effects of magnesium supplementation on serum magnesium concentration, CIPN severity, and sleep quality in CRC patients undergoing chemotherapy.Read full original descriptionShow less

Exploring the Effects of Magnesium Ions on Peripheral Neuropathy, Serum Magnesium Ion Concentration,Sleep Quality, and Quality of Life in Patients With Colorectal Cancer Receiving Chemotherapy.

Chemotherapy for colorectal cancer (CRC) is frequently complicated by chemotherapy-induced peripheral neuropathy (CIPN) and impaired sleep quality, significantly impacting patient quality of life. Low magnesium levels have been implicated in peripheral nerve dysfunction. This interventional study aims to investigate the effects of magnesium supplementation on serum magnesium concentration, CIPN severity, and sleep quality in CRC patients undergoing chemotherapy.

Study Design and Methods

This is a prospective, parallel-group, randomized controlled trial (RCT) utilizing a longitudinal design. Participants (CRC patients undergoing chemotherapy) will be randomly allocated to one of three groups:

* Experimental Group 1: Oral magnesium (400mg) supplementation. * Experimental Group 2: Oral magnesium (400mg}) supplementation and magnesium solution foot baths. * Control Group: Standard care.

Measurements will be collected using structured questionnaires and blood samples during each chemotherapy cycle. The primary outcomes will be assessed using:

* Serum Magnesium Concentration * CIPN Severity: Functional Assessment of Cancer Therapy/Gynecologic Oncology Group-neurotoxicity (FACT/GOG-Ntx) scale. * Sleep Quality: Verran and Snyder-Halpern Sleep Scale (VSH). Primary Research Questions (Hypotheses)

1. Can the magnesium intervention (oral and/or foot baths) effectively increase the serum magnesium concentration in CRC patients? 2. Can the magnesium intervention alleviate or improve the severity of CIPN? 3. Can the magnesium intervention improve the sleep quality of CRC patients during chemotherapy? The intervention groups will be compared against the control group to determine if the magnesium interventions lead to superior improvement in the measured outcomes.

Inclusion: a. Patients diagnosed with colorectal cancer by pathology; b. Age ≥ 20 years; c. Conscious; d. Able to communicate fluently in Mandarin and Taiwanese; e. Patients who have received or are expected to begin chemotherapy (Oxaliplatin).

Exclusion: b. Patients receiving intravenous nutrition; h. Patients with renal insufficiency; j. Patients allergic to any of the ingredients; a. ECOG (Eastern Cooperative Oncology Group) ≥2 points; c. Patients with pre-existing neuropathy; d. Patients with skin wounds; e. Patients with implanted pacemakers; f. Patients with phenylketonuria; g. Patients with diarrhea; i. Patients with hypermagnesemia.

ClinicalTrials.gov NCT07346469