Evidence map›Paper›PMID 40181005›Full record

Trial reportScientific reports2025

Pain control following impacted mandibular third molar surgery: a comparison of the effectiveness of two different protocols.

Kamis Gaballah, Tuleen Eldohaji, Maha El Tannir, Roula Shaban, Ruaa Habib, Kamran Ali

2 registry-linked trialsAbstract readRandomized Controlled TrialComparative Study
In one paragraph

Trial report in Scientific reports, 2025. 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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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.

NCT06514222 early_phase1unknown statusnot on this map

Pain Control Following Impacted Mandibular Third Molar Surgery: A Comparison of the Effectiveness of Two Different Protocols

TypeinterventionalSponsorUniversity of SharjahRan2024 to 2024Enrolled56ConditionsPost Operative Pain, Impacted Third Molar ToothArmsParacetamol and Ibuprofen. The combination of the Paracetamol and Ibuprofen will be given together every 8 hours, Paracetamol and Ibuprofen. The combination of the Paracetamol and Ibuprofen will be given alternatively every four hours
NCT07554963 phase4not yet recruitingnot on this mapstarted 2026, after this paper: background citation

Effect of Preoperative 4 mg Submucosal Dexamethasone on Postoperative Discomfort After Impacted Mandibular Third Molar Surgery: A Randomized Controlled Trial

TypeinterventionalSponsorHayat Abad Medical Complex, PeshawarRan2026 to 2026Enrolled268ConditionsImpacted Mandibular Third Molar, Postoperative Pain, TrismusArmsDexamethasone, No intervention
3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. 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

6 authors.

Kamis GaballahDepartment of Oral and Craniofacial Sciences, College of Dental Medicine, University of Sharjah, Sharjah, United Arab Emirates. kyounus@sharjah.ac.ae.ORCID https://orcid.org/0000-0002-6823-1388
Tuleen EldohajiIntern Dentists, University Dental Hospital, University of Sharjah, Sharjah, United Arab Emirates.
Maha El TannirIntern Dentists, University Dental Hospital, University of Sharjah, Sharjah, United Arab Emirates.
Roula ShabanIntern Dentists, University Dental Hospital, University of Sharjah, Sharjah, United Arab Emirates.
Ruaa HabibIntern Dentists, University Dental Hospital, University of Sharjah, Sharjah, United Arab Emirates.
Kamran AliQU Health College of Dental Medicine, Qatar University, Doha, 2713, Qatar.ORCID https://orcid.org/0000-0002-3122-6729

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The use of multimodal analgesia is a common practice in clinical settings, where a combination of drugs with different mechanisms of action is used to enhance the effectiveness of an analgesic and reduce its adverse effects. This study aimed to compare the efficacy of concurrent ibuprofen and paracetamol with alternate administration in the management of postoperative pain after the surgical removal of impacted mandibular third molars. A single-center, double-masked, parallel-group, randomized controlled clinical trial involved 56 patients undergoing scheduled surgical extraction of impacted mandibular third molars. Patients were randomly assigned to either Group A (Control), where they were instructed to take one tablet of ibuprofen 400 mg and two tablets of paracetamol 500 mg together every 8 h for 48 h, or Group B (Study), where they were instructed to take one tablet of ibuprofen 400 mg and two tablets of paracetamol 500 mg alternatively every 4 h for 48 h. The primary outcome measure was the intensity of postoperative pain, which was evaluated using a Visual Analogue Scale (VAS) ranging from 0 to 10. The secondary outcome measure was the timing of the onset of the analgesic effect, the duration of pain relief, the frequency of rescue drug administration, and the time interval between taking the recommended medication and the need for rescue medication. Investigators involved in analyzing the patients' responses were blinded to the pain control regime used by the participants. Pain intensity during the first 48 h after the extractions showed that most participants experienced "some pain," including 50% in Group A and 35.7% in Group B. The percentage of patients reporting "no pain" was higher in group B than in group A, although the difference was not statistically significant (p = 0.495). More than half of the participants (53%) in group A reported needing an extra dose in the 48-hour follow-up period, while 85% in group B reported pain relief (p = 0.002). When correlating the mean pain score to the complexity level, in patients with moderate complexity of extraction, higher pain scores were recorded in group B. The findings of this study show that the combination of Paracetamol and Ibuprofen are well-tolerated and effective option for post operative pain after surgical removal of mandibular third molars. Use of Paracetamol and Ibuprofen alternatively in the first 48 h showed a more effective pain control compared to concurrent use of these medications. However given the small sample size and patients recruited from a single center, multicenter studies with a bigger sample size and stratified complexity groups would enhance the generalizability of the findings.This trial protocol was registered with ClinicalTrials.gov (Registration No: NCT06514222 dated 23/07/2024).

Indexed as

AcetaminophenIbuprofenMolar, ThirdPain ManagementPostoperative PainTooth ExtractionTooth, ImpactedAdolescentAdultAnalgesics, Non-NarcoticDouble-Blind MethodFemaleHumansMaleMandiblePain MeasurementAcetaminophenAnalgesics, Non-NarcoticIbuprofenIbuprofenPainParacetamolPostoperative careThird molar surgery

Identifiers

PMID40181005
PMCPMC11969014

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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.