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PBC Induced Fatigue Treated With Thiamine

PBC Induced Fatigue Treated With Thiamine (PIFT) - The Effect of Oral Thiamine Supplement in 4 Weeks to Patients With Primary Biliary Cholangitis (PBC) and Chronic Fatigue. A Randomised Placebo Controlled Crossover Study

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04893993
Acronym
PIFT
Enrollment
36
Registered
2021-05-20
Start date
2021-05-12
Completion date
2023-12-31
Last updated
2021-05-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Primary Biliary Cirrhosis

Brief summary

Primary biliary cholangitis (PBC) is a chronic autoimmune liver disease characterised by destruction of the intrahepatic bile ducts leading to liver inflammation and fibrosis, and ultimately liver cirrhosis and end-stage liver disease. More than 50% of patients with PBC suffer from chronic fatigue, and approximately 20% suffer from severe fatigue with negative impact on their quality of life. Although fatigue is a large problem in patients with PBC, no effective treatments are available. A Danish intervention study have shown that high dose oral thiamine (Vitamin B1) were effective in treating chronic fatigue in patients with inflammatory bowel disease. In this study, only few and minor adverse events to thiamine treatment were observed. Although the precise mechanism of work remains unknown, the investigators see no reason that this cannot be transferred topatients with PBC. Hence, the investigators aim to conduct a study investigating the use of oral thiamine in chronic fatigued patients with PBC. The study will be conducted as a double-blinded, placebo-controlled, randomised, crossover trial including 36 patients with PBC and with a higher fatigue level than in the general population for more than six months. The patients will be randomised into one of two 3x4 weeks setups; 1) thiamine for four weeks followed by four weeks washout and finally four weeks of placebo or 2) placebo for four weeks followed by four weeks washout and finally four weeks of thiamine. The primary endpoint is to investigate the fatigue-level before and after treatment with thiamine and placebo using every patient as their own control. Fatigue-level will be measured using international validated questionnaires. The doses of thiamine are calculated based on the patient gender and weight. All patients will be included in the outpatient clinic at the Department of Hepatology and Gastroenterology at Aarhus University Hospital.

Interventions

DRUGThiamine

Tablets. 300mg/tablet. Dosage depends on gender and weight

DRUGPlacebo

Tablets. Same number of tablets as Thiamine

Sponsors

Aarhus University Hospital
CollaboratorOTHER
Hospitalsapoteket Region Midtjylland
CollaboratorUNKNOWN
GCP-unit at Aarhus University Hospital, Aarhus, Denmark
CollaboratorOTHER
Region Hovedstadens Apotek
CollaboratorOTHER_GOV
Henning Grønbæk
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* PBC for more than 3 months * PBC-40 fatigue score \>32 * Fatigued for at least 6 months

Exclusion criteria

* Comorbidity that can explain fatigue * Non-compliant patients * Pregnancy * Expected surgical interventions during the study period * Chronic kidney disease (eGFR\<60)

Design outcomes

Primary

MeasureTime frameDescription
FatigueAfter 4 weeks active treatmentChange in levels of fatigue measured by the Primary biliary cholangitis-40 (PBC-40) fatigue domain. The fatigue domain measures the severity of fatigue on a scale from 11-55, where 55 is maximun fatigue. A change in PBC-40 fatigue domain of 5 points or more is regarded as a clinical relevant change.

Secondary

MeasureTime frameDescription
Disease-specific Quality of LifeWeek 4, 8 and 12Changes in Health-related Quality of life, measured by the disease specific Primary biliary Cholangitis-40 (PBC-40).
Health-related Quality of LifeWeek 4, 8 and 12Changes in Health-related Quality of Life, measured by the generic EQ-5D-5L tool (mainly the VAS-scale from 0-100, where 100 is best).
FatigueWeek 8 and 12Change in levels of fatigue measured by the Primary biliary cholangitis-40 (PBC-40) fatigue domain. The fatigue domain measures the severity of fatigue on a scale from 11-55, where 55 is maximun fatigue. A change in PBC-40 fatigue domain of 5 points or more is regarded as a clinical relevant change.

Countries

Denmark

Contacts

Primary ContactHenning Grønbæk, Professor
henngroe@rm.dk+45 21679281

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026