Condition: Spinal Anesthesia Induced Hypotension · Geriatric · Internal Jugular Vein · Sponsor: Dr Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital
Spinal anesthesia-induced hypotension is a common and clinically significant complication in geriatric patients. Accurate preoperative assessment of intravascular volume status may help identify patients at risk. Internal jugular vein (IJV) ultrasonography is a noninvasive and easily applicable bedside method that reflects venous volume status. This prospective observational study aims to evaluate the role of preoperative IJV ultrasonographic measurements in predicting hypotension following spinal anesthesia in geriatric patients. Patients aged 65 years and older undergoing elective surgery under spinal anesthesia will be included. Preoperative IJV diameter, cross-sectional area, and collapsibility index will be measured using ultrasonography. Hemodynamic parameters will be monitored intraoperatively, and the occurrence of hypotension after spinal anesthesia will be recorded. The predictive value of IJV ultrasonographic parameters for post-spinal hypotension will be analyzed
This description comes directly from the study's public registry record.
Aylin N Gultekin, MD · +90 538 875 65 40 · aylinnilkondiloglu@gmail.com
Guldeniz ARGUN, phD · +90 533 623 0405 · guldargun@yahoo.com
Always discuss trial participation with your own doctor first.
| Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital | Ankara, YENİMAHALLE, Turkey (Türkiye) | Recruiting |
Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.
We email about this public record only. Unsubscribe anytime with one click. Never medical advice.
This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.
Source record: clinicaltrials.gov/study/NCT07411313