Clinical Trials Logo

Clinical Trial 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.


Clinical Trial 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. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05272475
Study type Interventional
Source Stony Brook University
Contact
Status Completed
Phase N/A
Start date March 16, 2022
Completion date May 12, 2022

See also
  Status Clinical Trial Phase
Completed NCT03826043 - THrombo-Embolic Event in Onco-hematology N/A
Recruiting NCT04274777 - The Relationship Between Lipid Peroxidation Products From Traumatic Brain Injury and Secondary Coagulation Disorders
Recruiting NCT03136510 - Evolution of Coagulation Activity in Non Valvular Atrial Fibrillation Patients Under Apixaban N/A
Completed NCT01588132 - Anfibatide Phase 1 Clinical Trial in Healthy Volunteers Phase 1
Recruiting NCT04488341 - Effect of Aerobic Exercises on Sex Hormones and Coagulation Factors in Postmenopausal Elderly Women N/A
Recruiting NCT04524637 - The Utility of Thromboelastography in Traumatic Brain Injury
Completed NCT03634215 - Estimation of Coagulation Factor XIII Activity Based on the Initial Plasma Fibrinogen Level in Trauma
Completed NCT05152420 - Study of Intravenous VMX-C001 in Healthy Subjects and in Combination With Selected Direct Oral Anticoagulants in Healthy Older Subjects Phase 1
Recruiting NCT05645081 - Extracellular Vesicles and Dysregulated Coagulation in the Prediction of Stroke
Completed NCT04322721 - Coagulopathy on the First Postoperative Day Predicts the Long-term Survival of Traumatic Brain Injury Patients
Completed NCT03267823 - INR Comparison Testing in Cardiac Surgery
Completed NCT04490759 - QStat Pilot Reference Range Study
Recruiting NCT04107818 - Comparison of Viscoelastic Measurement by ROTEM® Delta and ClotPro® in Trauma Patients.
Recruiting NCT05484830 - Coagulation in Acute Aortic Dissection N/A
Recruiting NCT04111120 - Heparin Like Effect in Acute Variceal Bleeding
Completed NCT05162339 - Inflammatory Bowel Disease and Thromboembolic Events
Completed NCT03555630 - Thromboelastogram in Postdelivery Preeclamptic Patients
Completed NCT01589172 - Evaluating the Use of Thromboelastography to Diagnose Coagulopathy After Traumatic Brain Injury
Recruiting NCT04278404 - Pharmacokinetics, Pharmacodynamics, and Safety Profile of Understudied Drugs Administered to Children Per Standard of Care (POPS)
Completed NCT03956836 - Perioperative Coagulopathy in Patients Undergoing Cytoreductive Surgery and HIPEC Intraperitoneal Chemotherapy (HIPEC)