Status:
COMPLETED
Premedication by Midazolam for Emergency Surgery
Lead Sponsor:
University Hospital, Lille
Conditions:
Anxiety
Eligibility:
All Genders
18-79 years
Phase:
PHASE4
Brief Summary
Preoperative anxiety is a subjective and painful experience and may have adverse psychological consequences and complicate anesthetic management. The aim of the study is to show the effect of premedic...
Eligibility Criteria
Inclusion
- major patient undergoing elective surgery under general anesthesia with tracheal intubation
- Anesthesia state 1 and 2
- preoperative fasting for 6 hours
- information and signed consent
- social security
- non pregnant women
Exclusion
- anesthesia state above 3
- midazolam sensibility
- pregnant or breastfeeding women
- ICU patients
- no consent
- pediatric surgery
- no social security
- no tracheal intubation
- required premedication in placebo group or midazolam sensibility in premedication group
Key Trial Info
Start Date :
July 1 2014
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
January 1 2016
Estimated Enrollment :
59 Patients enrolled
Trial Details
Trial ID
NCT02213302
Start Date
July 1 2014
End Date
January 1 2016
Last Update
February 11 2016
Active Locations (1)
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1
Emergency, University Hopital
Lille, France, 59000