Eligibility Module

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 @ 7:48 PM
Ignite Modification Date: 2025-12-24 @ 7:48 PM
NCT ID: NCT01901003
Eligibility Criteria: Inclusion Criteria: * male or female aged 18 to 70 years or more; * About a weight greater than 45 kg; * Subject to benefit from a scheduled surgery under general anesthesia; * Topic respecting the ambivalence clause defined below: 1. Having no cons-indication to the use of benzodiazepines; 2. Having no known allergy to benzodiazepines; 3. May be a candidate for the prescription of premedication; * Topic able to complete a self-administered questionnaire; * Subject has signed a written informed consent and agreeing to abide by the instructions of the Protocol Exclusion Criteria: * \- Topic of over 70 years; * Topic 45 kg or less; * Topic demanding to receive anxiolytic premedication; * Subject severe respiratory insufficiency; * Topic minor, pregnant or breastfeeding, about not being affiliated to the social security system; * Topic for which surgery is performed under local anesthesia; * Subject unable to perform only a self-administered questionnaire (inability to read French, severe cognitive impairment); * Subject to which the scheduled surgery may cause postoperative cognitive dysfunction (intracranial surgery, extracorporeal circulation); * Topic scheduled for obstetrical surgery or outpatient; * Subject treated with antipsychotic (neuroleptic or lithium); * Subject with cognitive impairment already documented (Alzheimer, dementia, neurological sequelae); * Subject active consumer of narcotics; * Subject has not signed informed consent.
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Maximum Age: 70 Years
Study: NCT01901003
Study Brief:
Protocol Section: NCT01901003