The Effect of Remote Ischemic Preconditioning on Postoperative Cognitive Dysfunction in Total Knee Replacement
- Conditions
- Knee Osteoarthritis
- Interventions
- Procedure: Remote ischemic preconditioning
- Registration Number
- NCT02478216
- Lead Sponsor
- Konkuk University Medical Center
- Brief Summary
The patients were allocated randomly to receive remote preconditioning group (RIPC group, R) or not (Control group, C) using sealed envelopes with the options inside the sealed envelope of R and C before anaesthesia induction. The registered nurse who did not participate in patient care and was blind to the study performed the all randomization process. All medical staffs who involved the patient care were blind to the study. All data were collected by trained observers who were blind to the study and did not participate in patient care
- Detailed Description
RIPC was performed just after anesthesia induction and before the tourniquet application for the operation site. The tourniquet was applied at the opposite site of thigh in the both groups. The thigh was covered with blanket to conceal the tourniquet inflation and deflation. For R group, 3 cycles of tourniquet inflation for 5 minutes with 2 × systemic systolic arterial blood pressure of arrival at operation room and deflation were performed. For C group, the tourniquet was applied with same manner for R group except inflation pressure of 0 mmHg. The tourniquet pressure according to the randomization was set by the registered nurse who participated in the patients' allocation. The monitor of tourniquet pressure was sealed for blindness.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 72
- patient who was planned to undergo total knee replacement surgery
- emergency operation
- underlying cerebrovascular disease
- underlying peripheral vascular disease
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description R group Remote ischemic preconditioning Remote ischemic preconditioning will be applied.
- Primary Outcome Measures
Name Time Method Incidence of cerebral desaturation during operation time (an expected average of 2 hours) cerebral saturation will be assessed by using near infrared spectroscopy
- Secondary Outcome Measures
Name Time Method Incidence of postoperative delirium up to postoperative 7 days postoperative delirium will be assessed by using CAM method.
Trial Locations
- Locations (1)
Konkuk University Medical Center
🇰🇷Seoul, Korea, Republic of