Evidence map›Paper›PMID 41323006›Full record

ArticleCureus2025

Randomized, Double-Blind, Placebo-Controlled, Dose-Ranging Comparison of the Analgesic Efficacy and Safety of Intravenous Ketoprofen, Tramadol, and Morphine After Bony Impacted Mandibular Third Molar Surgery.

Arya Babul, Aidan Gill, Sohi Ashraf, Momina Hussain, Najib Babul

Abstract read
In one paragraph

Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Arya BabulBiomedical Sciences, West Career and Technical Academy, Las Vegas, USA.
Aidan GillMedical Affairs, APG-PharmaConsulting GmbH, Zug, CHE.
Sohi AshrafCritical Care, MountainView Hospital, Las Vegas, USA.
Momina HussainGenomics, Chinese Academy of Tropical Agriculture Sciences, Sanya, CHN.
Najib BabulDrug Development, Cinergen, LLC, Las Vegas, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction Although opioids remain the standard of care for managing postsurgical pain, concerns persist regarding their safety, tolerability, and potential for addiction. Intravenous (IV) formulations of ketoprofen and tramadol have been widely available in numerous countries outside the United States and Canada. Methods This single-dose, single-center, double-blind, randomized study (n=185) evaluated the analgesic efficacy, dose-response relationship, duration of action, and safety of IV ketoprofen 50 mg (n=33) and 100 mg (n=31), IV tramadol 100 mg (n=33) and 150 mg (n=22), IV morphine 4 mg (n=33), and placebo (n=33) administered over two minutes upon the first occurrence of moderate-to-severe pain following surgical extraction of bony impacted mandibular third molars. Pain intensity and pain relief were assessed over eight hours. The primary efficacy endpoint was total pain relief over the first four hours (TOTPAR 0-4). Secondary efficacy endpoints included TOTPAR at additional time intervals, summed pain intensity difference (SPID), peak pain relief, peak pain intensity difference, time to rescue analgesia, patient global evaluation, and time to confirmed perceptible and meaningful pain relief. Safety assessments included volunteered and observed adverse events (AEs). Results For TOTPAR 0-4 and all other efficacy endpoints, IV ketoprofen 50 mg and 100 mg, and IV tramadol 100 mg and 150 mg were significantly superior to IV morphine 4 mg and placebo. IV ketoprofen at both doses also outperformed IV tramadol at both doses across the majority of outcome measures. No significant differences in efficacy were observed between IV morphine 4 mg and placebo. The proportion of subjects experiencing one or more AEs was comparable among the placebo, IV ketoprofen 50 mg, and IV ketoprofen 100 mg groups. In contrast, higher AE rates were reported in the IV tramadol and IV morphine groups relative to placebo. Dosing in the IV tramadol 150 mg group was discontinued early due to the occurrence of seizures in two patients (9%) immediately following administration. Conclusions Both IV ketoprofen and IV tramadol demonstrated superior analgesic efficacy compared to IV morphine and placebo in the management of postsurgical pain. Notably, IV ketoprofen consistently outperformed tramadol across efficacy endpoints. The lack of efficacy observed with IV morphine 4 mg raises concerns about potential analgesic assay insensitivity in postsurgical dental pain. The occurrence of seizures in subjects without known seizure risk factors highlights a potentially insufficient safety margin for tramadol in unselected patient populations.

Indexed as

acute painketoprofenmorphinepostsurgical painrandomized controlled trialseizuresthird molar extractiontramadol

Identifiers

PMID41323006
PMCPMC12662191

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.