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NCT05006378

Effect of Chamomile Intake on Blood Coagulation Tests in Healthy Volunteers

Completed NA Last updated 10 February 2022
What this trial tests

NA trial testing Chamomile Tea in Coagulation Disorder in 12 participants. Completed in 19 January 2022.

Timeline
31 August 2021
Primary endpoint
19 January 2022
19 January 2022

Quick facts

Lead sponsorStony Brook University
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingdouble
Primary purposescreening
Enrollment12
Start date31 August 2021
Primary completion19 January 2022
Estimated completion19 January 2022
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Stony Brook University

Who can join

Adults 18 to 75, any sex, with Coagulation Disorder. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Chamomile may possess anticoagulant effects based on the presence of coumarin-like compounds within the flower. This randomized, placebo-controlled complete crossover study will investigate the impact of chamomile ingestion on coagulation.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Effect of chamomile intake on blood coagulation tests in healthy volunteers: a randomized, placebo-controlled, crossover trial.
    Schwartz JA, Romeiser JL, Kimura R, Senzel L, et al · · 2023 · cited 4× · PMID 37730613 · DOI 10.1186/s13741-023-00339-7

Verify or expand the search:

Other trials of Chamomile Tea

Trials testing the same drug.

Other recruiting trials for Coagulation Disorder

Currently open trials in the same condition.

Other Stony Brook University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05006378.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing