Evaluation Of The Effects Of Changes In Operating Table Position On Perfusion Index And Spinal Anesthesia
Perfusion
1 other identifier
observational
150
1 country
1
Brief 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.
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 Feb 2026
Shorter than P25 for all trials
1 active site
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
February 3, 2026
CompletedStudy Start
First participant enrolled
February 5, 2026
CompletedFirst Posted
Study publicly available on registry
February 10, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 15, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
April 20, 2026
CompletedFebruary 11, 2026
February 1, 2026
2 months
February 3, 2026
February 9, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
perfusion index
The amount of increase over time will be recorded according to the basal perfusion index value.
5 min
Study Arms (2)
neutral group
Patients will be included who are positioned so that the operating table is neutral.
tilt group
Patients will be positioned on the operating table with an incline towards the side they will be operated on.
Eligibility 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.
You may qualify if:
- 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.
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Enes Celiklead
Study Sites (1)
Mardin Artuklu University Training and Research Hospital
Mardin, Artuklu, 47100, Turkey (Türkiye)
Related Publications (1)
Tapar H, Karaman S, Dogru S, Karaman T, Sahin A, Tapar GG, Altiparmak F, Suren M. The effect of patient positions on perfusion index. BMC Anesthesiol. 2018 Aug 17;18(1):111. doi: 10.1186/s12871-018-0571-z.
PMID: 30115011BACKGROUND
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- ANESTHESIOLOGIST
Study Record Dates
First Submitted
February 3, 2026
First Posted
February 10, 2026
Study Start
February 5, 2026
Primary Completion
April 15, 2026
Study Completion
April 20, 2026
Last Updated
February 11, 2026
Record last verified: 2026-02