CompletedNot Applicable

Pain and Acetaminophen in Women Study

United States200 participantsStarted 2019-11-15

Plain-language summary

The purpose of this study is to evaluate the influence of acetaminophen on pain response and inflammation.

Age range18 Years

SexFEMALE

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

✕. Visual impairment that would impair one's ability to read to the extent that they could not read items on paper or a computer screen.
✕. Stopping schooling prior to completing ninth grade.
✕. A history of liver disorder and/or alcohol abuse.
✕. A current prescription of a drug that contains acetaminophen.
✕. Allergy to acetaminophen
✕. A score on the Patient Health Questionnaire - 9 depressive symptom scale of 15 or greater.
✕. For normal weight participants, a history of overweight or obesity.

Baseline Prostaglandin level

Timeframe: Within the first 10 minutes of the two-hour session

Change in Prostaglandin level

Timeframe: Within the first 10 minutes of the two-hour session and approximately ten minutes prior to the end of the two-hour session.

Baseline C-Reactive Protein

Timeframe: Within the first 10 minutes of the two-hour session.

McGill Pain Questionnaire (baseline)

Timeframe: In the first hour of the two-hour session.

McGill Pain Questionnaire (change)

Timeframe: Within the first hour and again within the final 30 minutes of the two-hour session.

Visual Analog Scale for Pain (baseline)

Timeframe: In the first hour of the two-hour session.

Visual Analog Scale for Pain (change)

Timeframe: Within the first hour and again within the final 30 minutes of the two-hour session.

Stigma Situations Inventory

NCT IDNCT04573426

SponsorOhio State University

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2021-05-02