Clinical Trials Directory

Trials / Completed

CompletedNCT05272475

The Acute Effects of Chamomile Intake on Blood Coagulation Tests in Healthy Volunteers

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
8 (actual)
Sponsor
Stony Brook University · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Accepted

Summary

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

Detailed description

Subjects will be enrolled into two groups in a crossover fashion upon obtaining written informed consent. The two intervention groups include (1) chamomile tea intake and (2) chamomile extract intake. Subjects will consume a single preparation of chamomile tea or extract capsule, and partake in a minimum of three days washout period between interventions. Screening assays of coagulation will be obtained immediately before the ingestion of chamomile, two hours after ingestion, and four hours after ingestion over the course of a single day.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTChamomile TeaChamomile tea bags consumed by subjects as described in study arms section.
DIETARY_SUPPLEMENTChamomile Extract CapsuleChamomile extract capsules consumed by subjects as described in "Experimental: Chamomile Extract Capsule" study arms section.

Timeline

Start date
2022-03-16
Primary completion
2022-05-12
Completion
2022-05-12
First posted
2022-03-09
Last updated
2022-06-10

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT05272475. Inclusion in this directory is not an endorsement.