An observational study in Anesthesia and Infertility, sponsored by Ondokuz Mayıs University. Completed at 1 site in Turkey. Open to female participants aged 18 Years to 50 Years. Per ClinicalTrials.gov, last updated 2025-04-01.
Sponsored by Ondokuz Mayıs University · Observational
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.
Different personality traits, anxiety disorders, depression, and somatoform disorders are frequently encountered in women with infertility problems. Although there are many studies evaluating the relationship of anxiety with variables such as hemodynamic parameters, need for anesthetic medication, recovery times, postoperative pain and analgesic requirements, the relationship between personality traits and these variables has not been investigated.
In our study, considering that the anesthesia needs of these patients with a stressful negative factor such as infertility may be at different levels, preoperative evaluation of the patients with a personality questionnaire will provide better perioperative management, a better quality recovery and possibly a higher quality oocyte aspiration. In this study, it was aimed to investigate the amount of anesthetic agent consumption, recovery times, postoperative pain scores, analgesic requirements, involuntary movement, time to reach sufficient sedation depth, and patient satisfaction of patients thought to have sedation.
All patients will fill out Personality Belief Scale-Short Form (PBQ-S1) and Beck Anxiety Scale one day before the procedure and they will be registered.
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This study's enrollment of 90 is below the median of 200 across 714 observational studies indexed under Infertility.
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Female patients between 18-50 ages who will undergo oocyte pick up procedure with sedation
Exclusion Criteria:
patients who will receive sedoanalgesia for the oocyte retrieval procedure.
Other: PBQ-S1
All patients will fill out Personality Belief Scale-Short Form (PBQ-S1) and Beck Anxiety Scale one day before the procedure and they will be registered.
Propofol consumption
mg, from the beginning to the end of the transvaginal oocyte retrieval procedure
Time frame: from the beginning to the end of the transvaginal oocyte retrieval procedure)
Time until the Ramsey Sedation Score of 4 is reached
The period elapsed after the patient is transported to the operating table and the sedation protocol begins.
Time frame: -The period of time starting with the propofol injection until the Ramsey Sedation Score of 4
Amount of propofol (mg) used until the required sedation depth is reached
The amount of iv propofol administered until the Ramsey Sedation Score of 4 is obtained
Time frame: The period of time starting with the propofol injection until the Ramsey Sedation Score of 4
Systolic, diastolic and, mean Blood pressure (mm/Hg)
It will be monitored and documented every 5 minutes during the procedure.
Time frame: every 5 minutes during the procedure
Heart rate (beats/min)
It will be monitored and documented every 5 minutes during the procedure.
Time frame: every 5 minutes during the procedure.
Peripheral oxygen saturation (%)
(%): It will be monitored and documented every 5 minutes during the procedure.
Time frame: every 5 minutes during the procedure
Number of Involuntary movement during the procedure
The presence of involuntary movement will be documented during the procedure.
Time frame: during the procedure.
Postoperative pain (visual analog scale)
Pain status will be evaluated based on visual analog scale (VAS) at rest and after movement.every 30-minute intervals for one hour in the recovery room. Each VAS is scores 0-10 (0=no pain, 10=unbearable pain)
Time frame: After the procedure,every 30 minutes up to 1 hour
Analgesic consumption
The analgesic agents administered to the patients throughout the postoperative period will be documented.
Time frame: postoperatively up to 2 hours
Postoperative recovery time
The time until the Modified Aldrete Score reaches 9 points will be determined.
Time frame: postoperatively up to 2 hours
The incidences of post-operative nausea and vomiting (PONV)
the presence of nausea and vomiting will be recorded for 24 hours after procedure
Time frame: the time from the end of the procedure until discharge
Undesirable events and interventions
Bradycardia, hypotension, airway obstruction, hypoxia will be documented throughout the perioperative phase with the intervention.
Time frame: time between start of procedure and discharge
This study is completed, as verified in Mar 2025. You cannot join it, but the record below documents what was studied.
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Ondokuz Mayıs University