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NCT04630834

Ibuprofen Plus Acetaminophen for Enhanced Pain Reduction

Status unknown Phase 4 Last updated 14 April 2022
What this trial tests

Phase 4 trial testing Ibuprofen in Pain, Acute in 100 participants. Status unknown.

Timeline
30 March 2021
Primary endpoint
20 June 2022
30 June 2022

Quick facts

Lead sponsorNew York City Health and Hospitals Corporation
PhasePhase 4
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposetreatment
Enrollment100
Start date30 March 2021
Primary completion20 June 2022
Estimated completion30 June 2022
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

New York City Health and Hospitals Corporation

Who can join

Adults 3 to 20, any sex, with Pain, Acute. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Combination of analgesics with different modes of action have the potential to offer enhanced pain relief with reduced dosage. Ibuprofen and acetaminophen have different modes of action. Combination of ibuprofen and acetaminophen has shown enhanced analgesia in adult studies, with pediatric data limited to post-operative pain and dental pain. Our study objective is to evaluate the analgesic efficacy of oral acetaminophen plus ibuprofen versus ibuprofen plus placebo for the management of acute pain in a pediatric emergency department.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Ibuprofen

Trials testing the same drug.

Other recruiting trials for Pain, Acute

Currently open trials in the same condition.

Other New York City Health and Hospitals Corporation trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04630834.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing