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Metabolic Effects of Medium-Chain Fatty Acids in Patients with Medium-Chain Acyl-CoA Dehydrogenase Deficiency and Healthy Individuals (MEMCADD)

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University of Copenhagen

Status

Enrolling

Conditions

Medium-chain Acyl-CoA Dehydrogenase Deficiency

Treatments

Other: Medium-Chain Fatty Acid (MCFA)
Other: Long-Chain Fatty Acid (LCFA)

Study type

Interventional

Funder types

Other

Identifiers

NCT06623032
NNF22OC0074110 (Other Grant/Funding Number)
H-24044278

Details and patient eligibility

About

The aim of this project is to investigate the physiological effects of intake of long-chain fatty acids (LCFA) and medium-chain fatty acids (MCFA) in patients with Medium-Chain Acyl-CoA Dehydrogenase Deficiency (MCADD) and healthy individuals

Full description

Male and female MCADD patients and healthy individuals will be included in this study which is a randomized intervention study in a cross over design consisting of two separate test days.

The study involves two test days of four hours each, during which the participants ingests either medium-chain fatty acids (MCFA) or long-chain fatty acids (LCFA) in the form of triacylglycerol oils. The order of fatty acid oils ingested is determined by randomization.

Enrollment

30 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria MCADD patients:

  • Male or female
  • Age between 18-80 years old
  • Diagnosed Medium-chain acyl-CoA dehydrogenase deficiency (MCADD

Inclusion Criteria Healthy Participants:

  • Male or female
  • Age between 18-80 years old

Exclusion Criteria both MCADD patients and healthy participants:

  • Diabetes
  • Kidney- or liver disease
  • Use of beta blockers or diuretics
  • Pregnant, lactating or planning to become pregnant within the study period
  • Regular intake of substantial amounts of coconut oil, palm kernel oil or any other source abundant in MCFA
  • Ongoing cancer treatment
  • Metabolic or absorptive disorders, gastric bypass operation, or use of medication affecting metabolism or food absorption
  • Inability, physically or mentally, to comply with the procedure required by the study protocol as evaluated by the primary investigator, study manager or clinical responsible

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

30 participants in 2 patient groups

Healthy Participants
Experimental group
Treatment:
Other: Long-Chain Fatty Acid (LCFA)
Other: Medium-Chain Fatty Acid (MCFA)
MCADD Patients
Experimental group
Treatment:
Other: Long-Chain Fatty Acid (LCFA)
Other: Medium-Chain Fatty Acid (MCFA)

Trial contacts and locations

1

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Central trial contact

Andreas M Fritzen, Associate Professor; Kasper S Jørgensen, PhD student

Data sourced from clinicaltrials.gov

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