Evidence map›Paper›PMID 38874739›Full record

Trial reportDrugs in R&D2024

Efficacy of Co-Crystal of Tramadol-Celecoxib (CTC) in Patients with Acute Moderate-to-Severe Pain: A Pooled Analysis of Data from Two Phase 3 Randomized Clinical Trials.

Richard Langford, Eugene R Viscusi, Adelaida Morte, Jesús Cebrecos, Mariano Sust, José María Giménez-Arnau, Oscar de Leon-Casasola

2 registry-linked trialsAbstract readClinical Trial, Phase IIIRandomized Controlled Trial
In one paragraph

Trial report in Drugs in R&D, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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.

NCT02982161 phase3completednot on this map

A Randomized, Double-Blind, Multicenter, Placebo- and Active Comparator-Controlled Study to Evaluate Efficacy and Safety of MR308 in the Treatment of Acute Pain After Third Molar Tooth Extraction (STARDOM1).

TypeinterventionalSponsorMundipharma Research GmbH & Co KGRan2016 to 2018Enrolled818ConditionsAcute PainArmsMR308, Tramadol, Placebo
NCT03108482 phase3completednot on this map

A Randomized, Double-blind, Active- (Tramadol and Celecoxib) and Placebo-controlled, Parallel Groups, Phase 3 Clinical Trial to Establish the Efficacy of Co-crystal E-58425 for the Management of Moderate to Severe Post-surgical Pain After Bunionectomy.

TypeinterventionalSponsorEsteve Pharmaceuticals, S.A.Ran2017 to 2017Enrolled637ConditionsAcute Post-surgical PainArmsCo-crystal E-58425 (Tramadol/Celecoxib), Tramadol (Ultram®), Celecoxib (Celebrex®), Placebo
3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
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

7 authors.

Richard LangfordThe London Clinic, London, W1G 6BW, UK. richard.langford@me.com.ORCID http://orcid.org/0000-0002-8703-067X
Eugene R ViscusiDepartment of Anesthesiology, Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, PA, USA.ORCID http://orcid.org/0000-0003-0260-4396
Adelaida MorteESTEVE Pharmaceuticals S.A., Barcelona, Spain.ORCID http://orcid.org/0000-0002-3897-8966
Jesús CebrecosESTEVE Pharmaceuticals S.A., Barcelona, Spain.ORCID http://orcid.org/0000-0003-0238-8638
Mariano SustESTEVE Pharmaceuticals S.A., Barcelona, Spain.ORCID http://orcid.org/0000-0003-1908-9271
José María Giménez-ArnauESTEVE Pharmaceuticals S.A., Barcelona, Spain.ORCID http://orcid.org/0009-0003-2675-4919
Oscar de Leon-CasasolaDepartment of Anesthesiology, University of Buffalo/Roswell Park Cancer Institute, Buffalo, NY, USA.ORCID http://orcid.org/0000-0002-0837-9196

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesNew acute pain medications are needed that provide effective analgesia while minimizing side effects and opioid exposure. Clinical trials of co-crystal of tramadol-celecoxib (CTC) have demonstrated an improved benefit/risk profile versus tramadol or celecoxib alone. We pooled data from two phase 3 clinical trials to evaluate the efficacy of CTC 200 mg twice daily (BID) in acute moderate-to-severe pain.

methodsEfficacy data were pooled from STARDOM1 [acute pain following oral surgery (NCT02982161)] and ESTEVE-SUSA-301 [acute pain following bunionectomy (NCT03108482)]. The primary efficacy outcome was sum of pain intensity difference from 0 to 48 h (SPID

resultsA total of 344 patients received CTC 200 mg BID, 342 received tramadol 50 or 100 mg four times a day, 181 received celecoxib 100 mg BID, and 172 received placebo. The least-squares mean difference in SPID

conclusionsThis pooled analysis reinforces the efficacy profile of CTC versus tramadol and, given that CTC permits lower daily tramadol dosing and thereby reduces unnecessary opioid use, this highlights its improved benefit/risk profile and its potential for the management of moderate-to-severe pain.

Indexed as

Acute PainAnalgesics, OpioidCelecoxibTramadolAdultAgedClinical Trials, Phase III as TopicDrug CombinationsFemaleHumansMaleMiddle AgedPain MeasurementTreatment OutcomeAnalgesics, OpioidCelecoxibDrug CombinationsTramadol

Identifiers

PMID38874739
PMCPMC11315862

What OpenQuestion holds

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Registered trials

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.