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
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | Chamomile Tea | Chamomile tea bags consumed by subjects as described in study arms section. |
| DIETARY_SUPPLEMENT | Chamomile Extract Capsule | Chamomile 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.