Preoperative Evaluation on Perioperative Complications

CompletedOBSERVATIONAL
Enrollment

1,000

Participants

Timeline

Start Date

October 15, 2023

Primary Completion Date

April 1, 2024

Study Completion Date

April 1, 2024

Conditions
Perioperative Complication
Interventions
OTHER

Observational

Routine laboratory parameters requested from patients; Direct lung Radiograph and Electrocardiography results were evaluated and preoperative consultations and recommendations requested from the patients were recorded. Type of anesthesia, operation performed, operation duration, intraoperative blood and fluid losses, intraoperative and postoperative complications that develop within the first 24 hours, additional problems that develop (pain, postoperative nausea and vomiting, hypothermia, change of consciousness, bleeding and unplanned transfer to the intensive care unit). postanesthesia recovery The length of stay in the room, length of hospital stay, and method of discharge were recorded. The effects of preoperative laboratory, imaging methods and required consultations on intraoperative and postoperative complications in the first 24 hours were evaluated.

Trial Locations (1)

55090

Samsun University, Samsun

All Listed Sponsors
lead

Samsun University

OTHER

NCT06203171 - Preoperative Evaluation on Perioperative Complications | Biotech Hunter | Biotech Hunter