NCT02734511View on ClinicalTrials.gov

Efficiency and Safety of a Procedural Sedation by Propofol on Terminally Ill Patients With Refractory Pain

PHASE3CompletedINTERVENTIONAL
Enrollment

20

Participants

Timeline

Start Date

May 19, 2017

Primary Completion Date

September 26, 2019

Study Completion Date

September 26, 2019

Conditions
Refractory Pains
Interventions
DRUG

sedation with propofol

induction with propofol at 20mg/kg/h. Then, when the patient is sleeping, dosage is decreased to 6 mg/kg/h

Trial Locations (1)

06200

CHU de Nice - Hôpital de l'Archet, Nice

All Listed Sponsors
lead

Centre Hospitalier Universitaire de Nice

OTHER

NCT02734511 - Efficiency and Safety of a Procedural Sedation by Propofol on Terminally Ill Patients With Refractory Pain | Biotech Hunter | Biotech Hunter