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A Study of Oral Kavalactones Effect on Nurses

A Study of Oral Kavalactones Effect on Nurses

Recruiting
18 years and older
All
Phase N/A

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Overview

This research study is being done to assess the impact of taking Kava extract (Piper methysticum), a dietary supplement on cortisol in a healthy nursing population.

Eligibility

Inclusion Criteria:

  • Surgical services nurses at Mayo Clinic in Rochester, MN.
  • Able to participate fully in all aspects of the study.
  • Willing to use birth control for the duration of the study (if of childbearing potential).
  • Understood and signed study informed consent.

Exclusion Criteria:

  • Pregnant, nursing, or trying to conceive.
  • Persons with a menstrual cycle who are not willing and able to use an approved contraceptive during the study (female sterilization (tubal ligation, hysterectomy), IUD or another implant, oral or injectable contraceptive, contraceptive patch/ring, diaphragm/cervical cap, male sterilization (vasectomy), male condom, female condom, sponge/spermicide) (Persons who do not have sex with men can participate without the use of an approved contraceptive).
  • Use of kava or kava-containing products within the past 8 weeks.
  • Any prior adverse reaction or known sensitivity or allergy to kava or related botanicals (peppers).
  • Use of acetaminophen that cannot be discontinued or replaced with an NSAID during the study.
  • Use of oral corticosteroids (e.g., hydrocortisone) or other steroids (e.g., prednisone).
  • Alcohol use greater than 1 drink per day.
  • Use of kratom within the past 8 weeks.
  • Recent history of clinical depression or anxiety diagnosis.
  • Known significant liver disease or dysfunction.
  • Known significant kidney disease or dysfunction.
  • Known Addison's or Cushing's Disease.
  • Known catecholamine imbalance or medication use which influences catecholamine levels.
  • History or current diagnosis of cancer (except for successfully treated basal cell carcinoma diagnosed less than 5 years prior to screening or cancer in full remission more than 5 years after diagnosis).
  • Recent history or acute disease or unstable medical condition.
  • Surgery planned during the course of the trial.
  • A known history of any condition or factor judged by the investigator to preclude participation in the study or which might hinder adherence.

Study details
    Stress

NCT06177535

Mayo Clinic

21 October 2025

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FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

How safe are clinical trials?

Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
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