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Pharmacokinetic Behavior of Phenolic Acids Derived From Black Tea

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Unilever

Status

Completed

Conditions

Cardiovascular Diseases

Treatments

Dietary Supplement: Black tea and phenolic acids
Dietary Supplement: hot water

Study type

Interventional

Funder types

Industry

Identifiers

NCT01533857
FDS-BNH-0379

Details and patient eligibility

About

This study is set up to determine pharmacokinetics of phenolic acids after a single oral dose to healthy males.

Enrollment

12 patients

Sex

Male

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • healthy males
  • not smoking

Exclusion criteria

  • use of NSAIDS and/or antibiotics
  • no blood donation 1 months prior to screening

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

12 participants in 2 patient groups, including a placebo group

Black tea
Experimental group
Description:
black tea
Treatment:
Dietary Supplement: Black tea and phenolic acids
placebo
Placebo Comparator group
Treatment:
Dietary Supplement: hot water

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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