Status:
UNKNOWN
Perioperative Lignocaine and Sleep Disturbance
Lead Sponsor:
University of Liege
Conditions:
Sleep Disturbance
Eligibility:
MALE
18-65 years
Phase:
PHASE4
Brief Summary
The aim of this clinical trial is to study the effect of an intravenous infusion of lidocaïne in a multimodal analgesic protocol on the architecture sleep during the first postoperative night.
Detailed Description
To study the effect of lidocaïne, we plan to include 40 patients, randomized in 2 groups, undergoing open prostate surgery in this randomized placebo-controlled trial. Before anesthesia induction, th...
Eligibility Criteria
Inclusion
- Radical prostatectomy
Exclusion
- BMI \> 30
- Neurologic/psychiatric diseases or therapeutics, seizyres
- Cardiac disease, second or third degree atrioventricular block
- Obstructive sleep apnea syndrome
- History of liver or renal insufficiency
- and any contraindication to the anesthetic protocol of the study.
Key Trial Info
Start Date :
December 1 2017
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 1 2018
Estimated Enrollment :
40 Patients enrolled
Trial Details
Trial ID
NCT03317912
Start Date
December 1 2017
End Date
December 1 2018
Last Update
October 23 2017
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