Viewing Study NCT05916599



Ignite Creation Date: 2024-05-06 @ 7:10 PM
Last Modification Date: 2024-10-26 @ 3:01 PM
Study NCT ID: NCT05916599
Status: RECRUITING
Last Update Posted: 2023-06-23
First Post: 2023-05-03

Brief Title: Ultrasound in Evaluation of Preoperative Fluid Management of Hip Fracture Surgery Patients
Sponsor: Gaziosmanpasa Research and Education Hospital
Organization: Gaziosmanpasa Research and Education Hospital

Study Overview

Official Title: Evaluation of Ultrasound on Peroperative Fluid Management in Patients Undergoing Hip Surgery Under Spinal Anesthesia
Status: RECRUITING
Status Verified Date: 2023-06
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Goal directed fluid therapy is a new standard surgical procedure which is successful in patients undergoing hip revision arthroplasty There has been a reduction of postoperative complications most importantly surgery with a decrease inbleeding as well as in hospital and intensive care stays it is related The aim of this study is to evaluate effectiveness of pulmonary ultrasound score and vena cava collapse index measurements in the patients undergoing hip surgery under spinal anesthesia and relation with peroperative fluid management
Detailed Description: Patients who will undergo hip surgery under spinal anesthesia using the closed envelope method it will be randomized and divided into 2 groups

1The inferior vena cava collapse index IVC CI and lung ultrasound score LUS measurements and goal directed fluid therapy will be done 2 Group applying zero balance liquid therapy to patients with conventional methods is planned

1 Patients in the group will be started with fluid replasment at an hourly rate of 2mlkgh and with ultrasound measurement the infused fluid will be evaluated and regulated
2 Crystalloid liquid infusion at a rate of 2mlkghour will be administered to the patients in the group additional fluid replacement will be decided by monitoring bleeding and urinary output zero balance is aimed at patients Both groups were treated with spinal anesthesia in the postoperative period 120 minute IVC CI and the LUS score value will be checked

If the CI is below 50 and the LUS score is below 15 fluid management will be considered as successful

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None