Overview
Sufentanil is an opioid analgesic that is used as an adjunct in anesthesia, in balanced anesthesia, and as a primary anesthetic agent. It is administered by the intravenous, epidural and sublingual routes. Also known as Dsuvia, the sublingual form is used for the management of acute pain in adults that is severe to warrant the use of an opioid analgesic in certified medically supervised healthcare settings, including hospitals, surgical centers, and emergency departments . Consideration may be made in the future for the use of the sublingual form in the US military in cases where analgesia is required immediately . The sublingual form, manufactured by AcelRx Pharmaceuticals, Inc. (AcelRx), was approved on November 2, 2018 . This route of administration is intended to be a simple, effective, non-invasive analgesic option to enable healthcare professionals to rapidly manage acute pain without difficult intravenous or epidural administration , .
Indication
The indications for this drug are as follows:
Associated Conditions
- Acute Pain
- Severe Acute Pain
Research Report
A Comprehensive Monograph on Sufentanil (DrugBank ID: DB00708): Pharmacology, Clinical Use, and Risk Management
Section 1: Executive Summary
Sufentanil is a potent, small-molecule synthetic opioid analgesic belonging to the 4-anilidopiperidine class of drugs. As a thienyl derivative of its parent compound, fentanyl, it represents one of the most powerful opioids utilized in modern clinical practice.[1] Its pharmacological profile is defined by an exceptionally high affinity and selectivity for the μ-opioid receptor, resulting in an analgesic potency estimated to be 5 to 10 times that of fentanyl and 500 to 1,000 times that of morphine.[1] This extreme potency, combined with high lipophilicity, facilitates a rapid onset of action, making it a cornerstone of anesthetic and analgesic practice in specific, high-acuity medical environments.[4]
The clinical applications of sufentanil are highly specialized and reflect its unique pharmacodynamic and pharmacokinetic properties. It is primarily administered intravenously as an analgesic adjunct to maintain balanced general anesthesia or as a primary anesthetic agent, particularly in major surgical procedures such as cardiovascular and neurosurgery, where its ability to ensure hemodynamic stability by attenuating the sympathetic stress response is highly valued.[3] Additionally, it is used via the epidural route, typically in combination with a local anesthetic like bupivacaine, to provide effective analgesia during labor and vaginal delivery.[5] A significant innovation in its delivery is the development of a sublingual tablet formulation (Dsuvia®, Dzuveo®), approved for the management of severe, acute pain exclusively within certified, medically supervised healthcare settings.[6]
Clinical Trials
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Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2023/12/26 | Phase 3 | Not yet recruiting | |||
2023/11/03 | N/A | Completed | |||
2023/10/19 | Not Applicable | Recruiting | |||
2023/10/13 | Not Applicable | Recruiting | Centre Hospitalier Universitaire de Nīmes | ||
2023/10/05 | N/A | Completed | Poznan University of Medical Sciences | ||
2023/09/18 | Phase 4 | Completed | |||
2023/09/14 | Phase 4 | Recruiting | Hairong Chen | ||
2023/09/14 | Phase 2 | Recruiting | Maternal and Child Health Hospital of Hubei Province | ||
2023/08/21 | Not Applicable | Completed | |||
2023/06/13 | Phase 2 | Completed | Maternal and Child Health Hospital of Hubei Province |
FDA Drug Approvals
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Health Canada Drug Approvals
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CIMA AEMPS Drug Approvals
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Philippines FDA Drug Approvals
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UK EMC Drug Information
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