Effects of Patients' Hormone Levels on Sedoanalgesia

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18-45
SponsorIzmir City Hospital

About this trial

Investigastors hypothesis is that the need for anaesthetic agents is less in patients with high progesterone levels and more in patients with high estrogen levels.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Between 18-45 years old

ASA-I ASA-II patients who were sedated for oocyte pick-up between 1 June 2025 and 1 September 2025 at Izmir City Hospital

Patients whose hormone levels were measured in the preoperative period due to surgical indication and registered in the hospital data processing system

Disqualifiers

Lack of patient approvel

Diagnosed psychiatric disorder

Use of drugs affecting the central nervous system

Presence of chronic pain syndrome

Trial population

Between 18-45 years old * ASA-I ASA-II patients who were sedated for oocyte pick-up between 1 June 2025 and 1 September 2025 at Izmir City Hospital * Patients whose hormone levels were measured in the preoperative period due to surgical indication and registered in the hospital data processing system

Trial design

Design model

Other

Time perspective

Cross-sectional

Treatments tested in this trial

  • Anesthesia Maintenance

    Drug

    the amount of propofol required to achieve depth of anaesthesia in mg/kg/minute

Treatment groups

100 Participants
are divided into 1 treatment group
Group A: OPU patients1 intervention

Trial outcomes

Primary outcomes

1

Anesthetic consumptiom

the amount of propofol needed to provide adequate depth of anaesthesia in mg/kg/minute

Time frame
intraoperative

Secondary outcomes

1

Pulse oximeter

pulse oksimeter values at the begining, 10 minutes later and final

Time frame
intraoperative
2

hearth rate changes

Heart rate (bp/min) at the begining, 10 minutes later, final

Time frame
intraoperative
3

Blood pressure changes

Blood pressure values (mm/Hg) at the begining, 10 minutes later, final

Time frame
intraoperative

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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