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Clinical Trials in Turkey / NCT07400185
Starting soon Observational

Evaluation Of The Effects Of Changes In Operating Table Position On Perfusion Index And Spinal Anesthesia

NCT07400185 · tracked via the Priya Life Science Turkey tracker
Sponsor
Enes Celik
Phase
Observational
Started
2026-02-05
Last updated
2026-02-11

Condition(s) studied

Perfusion IndexPosition Differences

Study summary

The aim of this observational study is to investigate how table position affects the development of block in patients undergoing spinal anesthesia. Perfusion index measurements will be used to answer this question. Patients who will undergo perfusion index measurement during surgery will be included in the study. These patients will be compared with patients whose anesthesiologists chose not to position them on the operating table. The study is planned to continue for approximately 40 days, and the data collected during this period will be used for evaluation.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Patients who will undergo lower extremity surgery within the specified time frame, are in ASA 1-3 risk group, have no additional medical conditions, and will receive spinal anesthesia. Exclusion Criteria: * Patients under 18 and over 65 years of age Patients who have received anesthesia other than spinal anesthesia Patients with peripheral artery disease Patients with nail polish, etc. on their nails

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Mardin Artuklu University Training and Research Hospital Mardin Artuklu

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07400185 on ClinicalTrials.gov ↗ ← All trials in Turkey