Effects of Patients' Hormone Levels on Sedoanalgesia
Observation of the Effect of Patients' Hormone Levels on Sedoanalgesia in Oocyte Pcik-Up: Prospective Observational Study
1 other identifier
observational
100
0 countries
N/A
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Jan 2026
Shorter than P25 for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
May 26, 2025
CompletedFirst Posted
Study publicly available on registry
January 30, 2026
CompletedStudy Start
First participant enrolled
January 30, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
April 30, 2026
CompletedJanuary 30, 2026
December 1, 2025
1 month
May 26, 2025
January 28, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Anesthetic consumptiom
the amount of propofol needed to provide adequate depth of anaesthesia in mg/kg/minute
intraoperative
Secondary Outcomes (3)
Pulse oximeter
intraoperative
hearth rate changes
intraoperative
Blood pressure changes
intraoperative
Study Arms (1)
OPU patients
patients progesteron estrogen levels and progesteron/estrogen ratios
Interventions
the amount of propofol required to achieve depth of anaesthesia in mg/kg/minute
Eligibility Criteria
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
You may qualify if:
- 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
You may not qualify if:
- Lack of patient approvel
- Diagnosed psychiatric disorder
- Use of drugs affecting the central nervous system
- Presence of chronic pain syndrome
- History of continuous analgesic use due to chronic pain
- Hepatic and/or renal insufficiency
- BMI\>30
- Changing the method of anaesthesia for any reason
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Related Publications (1)
Lee J, Lee J, Ko S. The relationship between serum progesterone concentration and anesthetic and analgesic requirements: a prospective observational study of parturients undergoing cesarean delivery. Anesth Analg. 2014 Oct;119(4):901-905. doi: 10.1213/ANE.0000000000000366.
PMID: 25036373RESULT
Study Officials
- STUDY CHAIR
Halide Hande Şahinkaya, MD
Izmir City Hospital, Anesthesiology and Reanimation Department
- STUDY CHAIR
Tuba Kuvvet Yoldaş, MD
Izmir City Hospital, Anesthesiology and Reanimation Department
- STUDY CHAIR
Zeki Tuncer Tekgul, Prof. Dr.
Izmir City Hospital, Anesthesiology and Reanimation Department
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER GOV
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- MD
Study Record Dates
First Submitted
May 26, 2025
First Posted
January 30, 2026
Study Start
January 30, 2026
Primary Completion
March 1, 2026
Study Completion
April 30, 2026
Last Updated
January 30, 2026
Record last verified: 2025-12