Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
This is an investigational combination therapy of lidocaine and magnesium sulfate evaluated in a Phase 4 randomized, double-blind, placebo-controlled trial conducted by the University of Wisconsin, Madison. The study (ClinicalTrials.gov identifier NCT01342510) was designed to test whether pretreatment with intravenous lidocaine (50 mg) combined with magnesium sulfate (0.25 g) would have an additive effect in reducing propofol injection pain compared to monotherapies or saline placebo. Lidocaine is a local anesthetic that blocks voltage-gated sodium channels, while magnesium sulfate acts as an NMDA receptor antagonist and vasodilator. The trial concluded that the combination did not provide additional benefit over lidocaine alone for reducing propofol injection pain.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on lidocaine + magnesium sulfate.