Management of Moderate to Severe Monotraumatic Pain With Sublingual Sufentanil in an Emergency Situation.
Recruiting now · Phase 3
Conditions studied: Pain Management
In brief
Pain is a common reason for emergency department (ED) visits. However, studies suggest that emergency physicians may not always provide optimal analgesic treatment due to various factors, such as time constraints, demographic factors like gender and age, and concerns about opioid use. As a result, patients with moderate to severe pain often experience long delays before receiving analgesia and may even be discharged with unresolved pain or suboptimal treatment. Additionally, diagnostic procedures for patients with isolated trauma (e.g., clinical examinations, radiographs) can lead to variations in pain levels, making it difficult to assess the effectiveness of analgesia. A commonly used treatment for moderate to severe pain is intravenous opioid administration. However, this approach requires longer wait times, complex titration, and significant resources (beds, nurses, equipment), which may be limited during peak hours. While oral opioids require fewer resources, their delayed onset and limited titratability restrict their use for severe pain. The sublingual sufentanil tablet (30 mcg), delivered via a single-dose applicator, was developed for patients with moderate to severe pain in emergency or outpatient surgical settings. Its unique pharmacokinetic and pharmacodynamic properties could offer advantages in non-invasive acute pain management. Sublingual sufentanil received market authorization in June 2018 for the treatment of moderate to severe acute pain in adults and is already used in many hospitals. However, further studies are needed to confirm its effectiveness and potential superiority in pain management. The objective of this study is to evaluate the effectiveness of 30 mcg sublingual sufentanil in patients admitted for moderate to severe pain due to isolated trauma. This will be compared to the standard pain management protocol used in the Clermont-Ferrand emergency department, focusing on pain score variations using a numerical rating scale (0-10)
Key facts
- Study ID
- NCT06917651
- Run by
- University Hospital, Clermont-Ferrand
- People needed
- 300
- Starts
- 2025-04-22
- Expected to finish
- 2027-04-22
- Last updated by the study team
- 2026-04-28
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Adult patient
- Patient with a pain rating on the Numerical Rating Scale (NRS) ≥ 4
- Pain of monotraumatic origin in the upper or lower limb
- Glasgow Coma Scale = 15
- SaO2 > 95% in ambient air
You may not qualify if…
- Polytrauma
- Analgesic treatment within the 4 hours preceding admission (except paracetamol)
- Woman of childbearing age without effective contraception, declaring pregnancy or at risk of pregnancy, breastfeeding woman, or positive pregnancy test at inclusion
- Patient requiring intravenous access upon admission (e.g., displaced open fracture)
- Contraindication or allergy to any of the molecules in the analgesia protocol
- Refusal to participate
- Known substance abuse or psychiatric disorders
- Known oxygen dependence or COPD
- Not affiliated with social security
- Patient under guardianship, curatorship, deprived of liberty, or under legal protection
- Patient who does not speak or read French
Where it is running
- CHU de Clermont-Ferrand, Clermont-Ferrand — France, France (enrolling)
Full record on ClinicalTrials.gov
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