Last reviewed · How we verify

lidocaine+adjunct tramadol

Bagcilar Training and Research Hospital · Phase 3 active Small molecule

Lidocaine is a local anesthetic that blocks sodium channels to prevent nerve impulses, while tramadol is a weak opioid agonist that also inhibits serotonin and norepinephrine reuptake.

Lidocaine is a local anesthetic that blocks sodium channels to prevent nerve impulses, while tramadol is a weak opioid agonist that also inhibits serotonin and norepinephrine reuptake. Used for Postoperative pain, acute pain, chronic pain.

At a glance

Generic namelidocaine+adjunct tramadol
Also known astramadol
SponsorBagcilar Training and Research Hospital
Drug classLocal anesthetic, weak opioid agonist
TargetVoltage-gated sodium channels, mu-opioid receptor, serotonin transporter, norepinephrine transporter
ModalitySmall molecule
Therapeutic areaPain management
PhasePhase 3

Mechanism of action

Lidocaine's mechanism of action is primarily through the blockade of voltage-gated sodium channels, preventing the initiation and transmission of nerve impulses. Tramadol, on the other hand, acts as a weak agonist at the mu-opioid receptor, as well as an inhibitor of the serotonin and norepinephrine transporters, leading to increased levels of these neurotransmitters in the synaptic cleft.

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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