Evaluation Of The Effects Of Changes In Operating Table Position On Perfusion Index And Spinal Anesthesia
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-65
SponsorEnes Celik
About this trial
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 criteria
Qualifiers
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.
Disqualifiers
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
Trial design
Treatments tested in this trial
- Not listed
Trial groups
150 Participants
are grouped into 2 trial groupsSponsors and collaborators
Enes Celik
Lead sponsor
Mardin Artuklu University
Sponsor institution
Source ClinicalTrials.gov