Evidence map›Paper›PMID 40779077›Full record

Trial reportEuropean journal of orthopaedic surgery & traumatology : orthopedie traumatologie2025

Intrathecal nalbuphine at two doses reduces opioid use and pain after total knee arthroplasty: a randomized controlled trial.

Chawisachon Nonsri, Inthiporn Kositanurit, Apirak Tewaritruangsri, Kornthip Jeephet, Piti Rattanaprichavej, Artit Laoruengthana

Abstract readRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in European journal of orthopaedic surgery & traumatology : orthopedie traumatologie, 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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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

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

6 authors.

Chawisachon NonsriNaresuan University, Phitsanulok, Thailand.
Inthiporn KositanuritNaresuan University, Phitsanulok, Thailand. inthipornk@nu.ac.th.
Apirak TewaritruangsriNakhonpathom hospital, Nakhonpathom, Thailand. kar_ipa@hotmail.com.
Kornthip JeephetNaresuan University, Phitsanulok, Thailand.
Piti RattanaprichavejNaresuan University, Phitsanulok, Thailand.
Artit LaoruengthanaNaresuan University, Phitsanulok, Thailand.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThis study aimed to assess the efficacy of different-dose intrathecal nalbuphine (ITN) in addition to adductor canal block (ACB) and its associated side effects.

methodsThis prospective randomized double-blinded controlled trial recruited 42 patients undergoing TKA at Naresuan University Hospital who received spinal anesthesia and ACB into three groups, each with 14 patients: Group A (control), Group B (additional ITN 0.8 mg), and Group C (additional ITN 1.2 mg). The primary outcome was the numeric rating scale (NRS) at rest and during movement at various time points. The secondary outcomes included the cumulative morphine use (CMU) and side effects.

resultsForty-two patients (group A = 14; group B = 14; group C = 14) were randomized. All patients were analyzed. The group C had significantly lower NRS at rest at 6, 12, 24, and 48 h postoperatively, and significantly lower NRS during movement at 6 and 36 h postoperatively when compared to group A. There was no significant difference in NRS between group C and B, or between group B and A. The group B and C required significantly less CMU than the group A during the first 24, 48, and 72 h after TKA. The side effects, which included nausea, vomiting, drowsiness, respiratory depression, and shivering, were not significantly different among the groups.

conclusionAdditional ITN, both 0.8 and 1.2 mg doses, effectively reduces CMU during the first 72 h after TKA. Given higher-dose ITN up to 1.2 mg provides benefit by further reducing pain scores, without increased side effects. TRIAL REGISTRATION CLINICAL TRIALS: TCTR20241012005, October 12, 2024.

Indexed as

Analgesics, OpioidArthroplasty, Replacement, KneeNalbuphinePostoperative PainAgedAnesthesia, SpinalDose-Response Relationship, DrugDouble-Blind MethodFemaleHumansInjections, SpinalMaleMiddle AgedMorphinePain MeasurementProspective StudiesAnalgesics, OpioidMorphineNalbuphineIntrathecal nalbuphinePain managementPostoperative nausea and vomitingTotal knee arthroplasty

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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.