Evidence map›Paper›PMID 41623940›Full record

Trial reportPain research & management2026

A Randomized Trial Evaluating the Synergistic Effect of Parenteral Diclofenac and Paracetamol for Pain Management in Adult Males With Acute Limb Injury.

Isma Qureshi, Raheel S Qureshi, Tim Harris, Sameer A Pathan, Ashraf M El Malik, Mohd E Babiker, Mohamad A Jamali, Zain A Bhutta, Stephen H Thomas

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Pain research & management, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

1 citing paper in PubMed.

  1. Trial
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

9 authors.

Isma QureshiDepartment of Emergency Medicine, Hamad Medical Corporation, Doha, Qatar, hamad.qa.ORCID https://orcid.org/0000-0003-0952-0208
Raheel S QureshiDepartment of Emergency Medicine, Hamad Medical Corporation, Doha, Qatar, hamad.qa.
Tim HarrisDepartment of Emergency Medicine, Blizard Institute of Barts & the London School of Medicine, Queen Mary University of London, London, UK, qmul.ac.uk.
Sameer A PathanDepartment of Emergency Medicine, Hamad Medical Corporation, Doha, Qatar, hamad.qa.
Ashraf M El MalikDepartment of Pharmacy, Cleveland Clinic, Cleveland, Ohio, USA, clevelandclinic.org.
Mohd E BabikerDepartment of Emergency Medicine, Hamad Medical Corporation, Doha, Qatar, hamad.qa.
Mohamad A JamaliDepartment of Emergency Medicine, Hamad Medical Corporation, Doha, Qatar, hamad.qa.
Zain A BhuttaDepartment of Emergency Medicine, Hamad Medical Corporation, Doha, Qatar, hamad.qa.
Stephen H ThomasDepartment of Emergency Medicine, Blizard Institute of Barts & the London School of Medicine, Queen Mary University of London, London, UK, qmul.ac.uk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: In the emergency department (ED), commonly used analgesics for pain management are nonsteroidal anti-inflammatory drugs (NSAIDs), paracetamol, and opioids. The aim of this clinical trial was to evaluate the effectiveness of intravenous (IV) or oral (PO) paracetamol, combined with intramuscular (IM) diclofenac, in patients with acute limb injuries. Methods: This study utilized a double-blind, randomized controlled design to evaluate three different treatment groups. The trial included healthy adult males aged 18-65 years, who arrived at the ED with acute limb injuries, and an initial pain score of at least 5 on the Numerical Rating Scale (NRS). Participants were randomly assigned in equal numbers to one of three groups: one group received IM diclofenac (75 mg/3 mL), along with oral paracetamol (1000 mg); the second group was given IM diclofenac plus IV paracetamol (1000 mg in 100 mL); and the third group received IM diclofenac (75 mg/3 mL), accompanied by a placebo. The main goal of the study was to compare the average pain reduction among the three groups at 30 min after treatment (t30). Results: A total of 162 participants were recruited between October 2022 and February 2023. Pain levels were assessed at baseline (t0) and continued to be monitored up to 90 min after medication was administered (t90). The average reduction in pain scores for each group was as follows: diclofenac plus oral paracetamol resulted in a mean decrease of 2.5 ± 0.03, diclofenac plus IV paracetamol had a mean reduction of 2.6 ± 0.03, and diclofenac with placebo showed a mean decrease of 2.2 ± 0.04. These results indicate there was no statistically significant difference in pain relief among the three groups. Additionally, none of the groups required rescue pain medication, and no adverse events were reported in any group. Conclusion: The results demonstrate that the three treatment groups achieved similar levels of pain relief within the observed timeframe, offering no significant advantage in terms of speed or extent of pain reduction. Nonetheless, additional studies are warranted to explore the potential synergistic effects of combining paracetamol with NSAIDs via various administration routes, as well as to assess possible adverse events, and the necessity for supplemental analgesia.

Indexed as

AcetaminophenAnalgesics, Non-NarcoticAnti-Inflammatory Agents, Non-SteroidalDiclofenacExtremitiesPainPain ManagementAdolescentAdultAgedDouble-Blind MethodDrug SynergismDrug Therapy, CombinationHumansMaleMiddle AgedAcetaminophenAnalgesics, Non-NarcoticAnti-Inflammatory Agents, Non-SteroidalDiclofenac

Identifiers

PMID41623940
PMCPMC12859818

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Registered trials

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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.