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

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 design

Treatments tested in this trial

  • Anesthesia Maintenance

Treatment groups

100 Participants
are divided into 1 treatment group

Locations

This trial has no locations

Sponsors and collaborators