RecruitingPhase 3NCT07274254

Lidocaine for Opioid Sparing in Vaso-occlusive Crisis of Sickle Cell Disease


Sponsor

Nantes University Hospital

Enrollment

104 participants

Start Date

Jul 3, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of the study is to determine whether adding lidocaine to standard of care in pain management during severe vaso-occlusive crisis has an effect on the cumulative opioid consumption expressed as morphine milligram equivalent.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Lidocain, a drug called Placebo, and others for people with vaso-occlusive pain episode in sickle cell disease. The study is currently recruiting participants at 11 locations. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGLidocain

Lidocaine hydrochloride 20 mg/mL, solution, 20 mL ampoule for IV administration (25 ampoules) Administration : parenteral route on peripheral or central venous catheter. - Bolus of 1.5 mg/kg bolus dur

DRUGPlacebo

Placebo is 20 mL ampoules of sodium chloride (NaCl 0.9%) for injection Administration : parenteral route on peripheral or central venous catheter. * Bolus of 1.5 mg/kg bolus during 30 minutes, with a maxium dose of 180 mg (18mL) * Immediately followed by a continuous infusion of 1 mg/kg/h (max 120mg/h = 12mL/h) during 72 hours.

DRUGStandard of care

Standard of care


Locations(11)

CHU Bordeaux

Bordeaux, France

CHU Lille

Lille, France

CHU La Timone

Marseille, France

CHU de Nantes

Nantes, France

CHU Orléans

Orléans, France

Hôpital Tenon APHP

Paris, France

CHU Poitiers

Poitiers, France

CHU Rouen

Rouen, France

Oncopole Toulouse

Toulouse, France

CHRU Tours - Hôpital Bretonneau

Tours, France

CHU Guadeloupe

Les Abymes, Guadeloupe

View Full Details on ClinicalTrials.gov

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NCT07274254


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