Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 7:51 PM
Ignite Modification Date:
2025-12-24 @ 7:51 PM
NCT ID:
NCT01161004
Eligibility Criteria:
Inclusion Criteria:
* patients scheduled to receive general anesthesia with muscle relaxation
Exclusion Criteria:
* contra-indication to the administration of propofol, remifentanil, rocuronium and to the use of the Bispectral Index or NeuroSense monitor
* known drug allergy or hypersensitivity to a drug used in the study
* history of central brain injury
* patient treated with a psychotropic agent
* patient with a pacemaker
* severe renal insufficiency
* treatment by toremifene, flucloxacillin or fusidic acid in the preoperative or immediate postoperative period
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT01161004
Study Brief:
Protocol Section:
NCT01161004