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Remifentanil+Lidocaine

The First Affiliated Hospital of Zhengzhou University · FDA-approved active Small molecule

Remifentanil is an opioid agonist that binds mu receptors to provide analgesia and sedation, while lidocaine is a local anesthetic that blocks sodium channels to provide local pain relief.

Remifentanil is an opioid agonist that binds mu receptors to provide analgesia and sedation, while lidocaine is a local anesthetic that blocks sodium channels to provide local pain relief. Used for Intraoperative analgesia and sedation during general anesthesia, Local anesthesia during surgical procedures.

At a glance

Generic nameRemifentanil+Lidocaine
SponsorThe First Affiliated Hospital of Zhengzhou University
Drug classOpioid analgesic + Local anesthetic combination
TargetMu-opioid receptor (remifentanil); Voltage-gated sodium channels (lidocaine)
ModalitySmall molecule
Therapeutic areaAnesthesia, Pain Management
PhaseFDA-approved

Mechanism of action

Remifentanil is a potent synthetic opioid that acts as a mu-opioid receptor agonist, providing rapid-onset analgesia and sedation with quick offset due to rapid metabolism by non-specific plasma esterases. Lidocaine is a local anesthetic that blocks voltage-gated sodium channels in nerve fibers, preventing the initiation and propagation of action potentials to produce local anesthesia. The combination provides both systemic analgesia/sedation and local anesthetic effects.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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