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NCT05234216: COMFORT
Comparison of a Comfort Scale and a Numerical Pain Scale on Opioid Consumption After Surgery
NA trial testing Informed consent in Pain Management in 885 participants. Completed in 1 July 2022.
1 July 2022
Quick facts
| Lead sponsor | Rennes University Hospital |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 885 |
| Start date | 9 May 2022 |
| Primary completion | 1 July 2022 |
| Estimated completion | 1 July 2022 |
| Sites | 29 locations across France, Lebanon |
Drugs / interventions tested
- Informed consent
- Surgery
- Comfort scale
- Pain
- Questionnaires
Conditions studied
- Pain Management — all drugs for Pain Management →
- Analgesia — all drugs for Analgesia →
Sponsor
Rennes University Hospital
Who can join
18 and older, any sex, with Pain Management or Analgesia. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The objective is to show that the use of therapeutic communication tools, in this case a comfort scale, a low cost and simple to implement method, can reduce pain and therefore the consumption of opioids in the postoperative care unit. Our hypothesis is that the use of a comfort scale will lead to significant postoperative opioid sparing, and consequently to a decrease in the opioid-related side effects The aim of this study is to compare postoperative opioid consumption between patients whose pain is assessed by a numerical verbal scale and those assessed with a comfort scale.
Publications & conference data
2 peer-reviewed publications reference this trial (live from Europe PMC):
-
Effect of a comfort scale compared with a pain numerical rate scale on opioids consumption in postanaesthesia care unit: the COMFORT study.
Fusco N, Meuret L, Bernard F, Musellec H, et al · · 2024 · cited 2× · PMID 39244480 · DOI 10.1016/j.bja.2024.06.029 -
Comfort-Focused Assessment and Patient-Reported Experience After Regional versus General Anaesthesia: Post Hoc Analysis of a Cluster-Randomised Trial.
Maurice-Szamburski A, Rozier R, Fusco N, Meuret L, et al · · 2026 · PMID 41177344 · DOI 10.1016/j.accpm.2025.101660
Verify or expand the search:
- PubMed search for NCT05234216
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
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Other recruiting trials for Pain Management
Currently open trials in the same condition.
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Other Rennes University Hospital trials
Trials by the same sponsor.
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT05234216 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Rennes University Hospital
- Last refreshed: 23 September 2022
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05234216.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing