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Acetaminophen Randomized Controlled Trial | Clinical Trials | Clareo Health

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WITHDRAWNPhase 3NCT02737124

Acetaminophen Randomized Controlled Trial

Patients that are to undergo isolated meniscectomy will be randomized to 2 cohorts: one will take the FDA recommended dose of acetominophen (1000mg) 24hrs before surgery, one will be given a similarly...

Lead sponsor: NYU Langone Health•1 U.S. locations•View source on ClinicalTrials.gov

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Sponsors

Lead Sponsor

NYU Langone Health

Age

18 - 65 years

Sex

ALL

Healthy Volunteers

No

Inclusion Criteria

•Must be at least 18 years of age
•ASA Class I-II
•Patients scheduled for meniscectomy

Exclusion Criteria

•Contraindication to acetaminophen (hypersensitivity, extensive alcohol history, liver disease, actively breastfeeding)
•Legally incompetent or mentally impaired (e.g., minors, Alzheimer's subjects, dementia, etc.)
•Younger than 18 years of age or older than 65
•Any patient considered a vulnerable subject
•Patients on pain medication prior to surgery

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: July 26, 2018Terms

Trial snapshot

StatusWITHDRAWN

PhasePHASE3

Enrollment—

Start dateFeb 2017

Last updatedJul 26, 2018

Condition

Post Operative Pain

Locations shown

New York University Medical Center

New York, New York

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: July 26, 2018Data synced to Clareo: June 28, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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