Completed PHASE4 INTERVENTIONAL 2-arm NCT02244619

PO vs. IV Acetaminophen Given Perioperatively for 24 hr Post-op Pain Control Following Total Hip or Knee Replacement (KHEA)

Randomized, Double-Blind, Study Comparing Oral Acetaminophen Plus Intravenous (IV) Placebo to Oral Placebo Plus IV Acetaminophen Given Perioperatively for Controlling Pain in the 24hr Post-op Period After Total Hip or Knee Joint Replacement

Sponsor: Kettering Health Network

Conditions Post-op Pain

Interventions IV acetaminophen Oral acetaminophen

Updated 8 times since 2017 Last updated: Jul 21, 2017 Started: Sep 30, 2014 Primary completion: Apr 30, 2016 Completion: Apr 30, 2016

This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

A PHASE4 clinical study on Post-op Pain, this trial is completed. The trial is conducted by Kettering Health Network and has accumulated 8 data snapshots since 2014. Longitudinal tracking of this trial contributes to a broader understanding of treatment development timelines.

Status Flow

Change History

8 versions recorded

Sep 2024 — Present [monthly]

Completed PHASE4
Jul 2024 — Sep 2024 [monthly]

Completed PHASE4
Dec 2021 — Jul 2024 [monthly]

Completed PHASE4
Jan 2021 — Dec 2021 [monthly]

Completed PHASE4
Jun 2018 — Jan 2021 [monthly]

Completed PHASE4

▶ Show 3 earlier versions

Aug 2017 — Jun 2018 [monthly]

Completed PHASE4
Apr 2017 — Aug 2017 [monthly]

Completed PHASE4

Status: Recruiting → Completed
Jan 2017 — Apr 2017 [monthly]

Recruiting PHASE4

First recorded

Sep 2014

Trial started

Per CT.gov start date — pre-dates our first snapshot

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:

Kettering Health Network

Data source: Kettering Health Network

For direct contact, visit the study record on ClinicalTrials.gov .

Study Locations

• Kettering, United States