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Ropivacaine + Ketamine

Aga Khan University · FDA-approved active Small molecule

Ropivacaine blocks sodium channels to provide local anesthesia, while ketamine blocks NMDA receptors to provide analgesia and dissociative effects, together reducing pain and anesthetic requirements.

Ropivacaine blocks sodium channels to provide local anesthesia, while ketamine blocks NMDA receptors to provide analgesia and dissociative effects, together reducing pain and anesthetic requirements. Used for Local and regional anesthesia with enhanced analgesia, Perioperative pain management.

At a glance

Generic nameRopivacaine + Ketamine
SponsorAga Khan University
Drug classLocal anesthetic + NMDA receptor antagonist combination
TargetVoltage-gated sodium channels (ropivacaine); NMDA receptor (ketamine)
ModalitySmall molecule
Therapeutic areaAnesthesia and Pain Management
PhaseFDA-approved

Mechanism of action

Ropivacaine is a long-acting amide local anesthetic that reversibly inhibits sodium influx in nerve fibers, preventing action potential propagation and sensory transmission. Ketamine is a non-competitive NMDA receptor antagonist that provides analgesia, amnesia, and dissociation. The combination leverages synergistic analgesic and anesthetic effects, allowing lower doses of each agent and potentially reducing adverse effects associated with higher single-agent doses.

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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