The Relationship Between Personality Traits and Perioperative Anesthetic Drug Consumption (NCT06093789) | Clinical Trial Compass
CompletedNot Applicable
The Relationship Between Personality Traits and Perioperative Anesthetic Drug Consumption
Turkey (Türkiye)90 participantsStarted 2023-11-01
Plain-language summary
In this study, we aimed to examine the association between personality traits and amount of anesthetic drug consumption,of the patients who will receive sedoanalgesia for the oocyte retrieval procedure. As well as determining the anxiety scores in the preoperative period, the time to reach the desired sedation level, hemodynamic parameters in the perioperative period, peripheral oxygen saturation, EtCO2 value, postoperative pain, postanesthetic recovery, analgesic drug need, unconscious movement, and patient satisfaction.
Who can participate
Age range
18 Years – 50 Years
Sex
FEMALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* 18- 50 year-old elective patients who signed the informed consent form from ASA I-II patients scheduled for oocyte retrieval.
* Patients with sufficient education and mental capacity to complete in assessment scales and questionnaires.
* Patients without neurological disorders, psychological illnesses, or drug or alcohol abuse
* Patients without stimulant drug and alcohol consumption
* Absence of significant cardiovascular, respiratory, kidney or liver disease.
Exclusion Criteria:
* Psychiatric or neurological disorder
* Psychiatric drug use or alcohol consumption
* Pregnancy
* Presence of severe cardiac, hepatic or cerebrovascular disease
* History of allergy to local anesthetics or systemic opioids
* History of chronic pain
* Patients who are unable to evaluate scales and questionnaires
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Propofol consumption
Timeframe: from the beginning to the end of the transvaginal oocyte retrieval procedure)