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The Bioavailability of Mycoprotein

U

University of Exeter

Status

Completed

Conditions

Availability of Mycoprotein

Treatments

Other: Mycoprotein ingestion

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

To evaluate the bioavailability of mycoprotein, compared with a reference animal based protein, in a dose-response manner.

Enrollment

12 patients

Sex

Male

Ages

18 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy and aged 18-40 y
  • BMI between 18 and 30

Exclusion criteria

  • On medication
  • Family history of metabolic disease
  • Diagnosed with any metabolic or cardiovascular conditions
  • BMI < 18 or > 30

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

12 participants in 5 patient groups

Milk
Active Comparator group
Description:
Acute ingestion of 20 g milk protein
Treatment:
Other: Mycoprotein ingestion
20g
Experimental group
Description:
Acute ingestion of 20 g mycoprotein
Treatment:
Other: Mycoprotein ingestion
40g
Experimental group
Description:
Acute ingestion of 40 g mycoprotein
Treatment:
Other: Mycoprotein ingestion
60g
Experimental group
Description:
Acute ingestion of 60 g mycoprotein
Treatment:
Other: Mycoprotein ingestion
80g
Experimental group
Description:
Acute ingestion of 60 g mycoprotein
Treatment:
Other: Mycoprotein ingestion

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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