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lidocaine+adjunct tramadol
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 name | lidocaine+adjunct tramadol |
|---|---|
| Also known as | tramadol |
| Sponsor | Bagcilar Training and Research Hospital |
| Drug class | Local anesthetic, weak opioid agonist |
| Target | Voltage-gated sodium channels, mu-opioid receptor, serotonin transporter, norepinephrine transporter |
| Modality | Small molecule |
| Therapeutic area | Pain management |
| Phase | Phase 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
- Postoperative pain, acute pain, chronic pain
Common side effects
- Dizziness
- Nausea
- Vomiting
- Headache
- Drowsiness
Key clinical trials
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |
Competitive intelligence
For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:
- lidocaine+adjunct tramadol CI brief — competitive landscape report
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