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Clinical Trials in Denmark / NCT07338565
Recruiting Observational

Magnesium in Gastrointestinal Disease

NCT07338565 · tracked via the Priya Life Science Denmark tracker
Phase
Observational
Started
2025-11-03
Last updated
2026-01-14

Condition(s) studied

Colitis UlcerosaColitis UlcerativeCrohns DiseaseMorbus CrohnIleostomy - StomaIleostomaIleostomiesBile Acid DiarrheaBile Acid MalabsorptionMagnesium DeficiencyMagnesium LevelMagnesium

Study summary

Individuals with gastrointestinal diseases - such as Crohn's disease, ulcerative colitis, ileostomy, or bile acid diarrhoea - are at increased risk of magnesium deficiency. Magnesium is a vital mineral that supports many essential functions in the body, including muscle contraction, nerve signalling, heart rhythm, and bone health. Deficiency may contribute to fatigue, muscle cramps, abnormal heart rhythms, and reduce the quality of life.

The purpose of this study is to investigate the prevalence of magnesium deficiency in individuals with these conditions and to identify the most accurate and practical methods for assessing magnesium status in clinical care.

Although plasma magnesium is commonly used in routine blood tests, it represents only about 1% of the body's total magnesium and may not reflect true magnesium levels within cells or tissues. Hence, this study compares several different ways of measuring magnesium, including:

* Plasma magnesium
* Magnesium levels in red and white blood cells (PBMC, RBC, and buffy coat)
* Magnesium levels in muscle tissue (via biopsy)
* A magnesium retention test, based on how much magnesium is excreted after an infusion

The study includes four groups:

1. Patients with inflammatory bowel disease.
2. Patients with an ileostomy.
3. Patients with bile acid diarrhoea.
4. Healthy individuals (control group).

All participants will provide blood and urine samples, and some may undergo optional biopsies of muscle or intestinal tissue. Participants will also complete questionnaires and undergo tests of muscle strength and body composition.

The findings are expected to enhance the understanding and detection of magnesium deficiency in patients with gastrointestinal diseases and to aid in the development of more effective tools for identifying and treating this common yet often overlooked condition.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: \- Age 18 or older, mentally competent, and able to understand Danish. Group 1: \- Diagnosed with IBD (DK50X, Crohn's disease, or DK51X, ulcerative colitis), ileostomy (DZ932) or bile acid diarrhoea (DSK908B) (Se-HCAT scintigraphy showing residual activity \<10%). Group 2: \- Healthy individuals. Exclusion Criteria: * Pregnant or breastfeeding. * Use of oral magnesium supplements for more than 2 weeks before inclusion.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Department of Hepatology and Gastroenterology, Aarhus University Hospital Aarhus N Denmark Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07338565 on ClinicalTrials.gov ↗ ← All trials in Denmark