Clinical Trial

Effect of Spinal and General Anesthesia on Frontal QRS Axis in Patients Undergoing Total Knee Arthroplasty

Study acronym: TDP-QRS
Completed
View on ClinicalTrials.gov →
Summary
This prospective observational study aims to compare the effects of spinal and general anesthesia on frontal QRS axis in patients undergoing elective total knee arthroplasty. Adult patients aged 18 years and older with ASA physical status I to III will be included. Participants will be grouped according to the anesthesia technique applied in routine clinical practice. Standard 12-lead electrocardiography will be obtained preoperatively and postoperatively, and frontal QRS axis values will be recorded using the automatic measurements of the ECG device. The primary objective is to evaluate the preoperative-to-postoperative change in frontal QRS axis and to compare this change between patients receiving spinal anesthesia and those receiving general anesthesia. Demographic and perioperative variables, including comorbidities, intraoperative fluid administration, blood pressure, oxygen saturation, heart rate, and tourniquet time, will also be recorded. This study is designed to provide clinical information about the potential effects of anesthesia technique on cardiac electrical activity in patients undergoing total knee arthroplasty.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2026-04-20.
Trial Details
NCT Number NCT07551648
Lead Sponsor Elazıg Fethi Sekin Sehir Hastanesi
Conditions Total Knee Arthroplasty, Electrocardiographic Changes
Enrollment 140 participants
Start Date 2025-09-04
Primary Completion 2026-03-03 (estimated)
Study Completion 2026-03-10 (estimated)
Updated on ClinicalTrials.gov 2026-06-04