Safety of Spinal Anesthesia in Patients With Tibial Shaft Fracture: A Single-center Randomized, Controlled Trial.
General anesthesia
+ Spinal anesthesia
+ General anesthesia
Leg Injuries+1
+ Wounds and Injuries
+ Fractures, Bone
Supportive Care Study
Summary
Study start date: March 1, 2012
Actual date on which the first participant was enrolled.For some of the patients RA may be even more safe than GA. According to a large meta-analysis RA reduces the risk of several complications versus GA. Risk of deep vein thrombosis is reduced by 44% Risk of pulmonary embolism is reduced by 55 % Risk of major bleeding is reduced by 50% Risk of post operative pneumonia is reduced by 39% Risk of post operative respiratory is reduced by 59% It is generally thought that RA is safer than GA for example in patients with heart or pulmonary diseases. It is also known that the use of RA reduces postoperative need of opioids, which leads to improved respiratory function and reduced post operative disorientation, delirium and nausea. Purpose of the study: Our purpose is to gain more information of the safety of RA in patients with tibial fracture. Our hypothesis is that RA is equally safe with GA. Implementation: Research begins with a pilot study in which RA is compared with GA. There are about 65 tibial fractures operated in our centre every year. We randomize patients to GA group (n=25) and spinal anaesthesia group (n=25). We presume that RA is equally safe with GA. However, power analysis has been made presuming that RA will increase the risk of ACS. We calculated the sample size by assuming that the compartment pressure in RA group is 10 mmHg higher than in the GA group. GA will be inducted by fentanyl, propofol and rocuronium. GA will be maintained by sevofluran, fentanyl and rocuronium. Spinal-anaesthesia will be performed by using hyperbaric bupivacaine. The dose is 10-15 mg, depending on the needs of the patient. This will maintain RA in lower extremities for 2-4 hours, which is enough to operate a tibial shaft fracture. In both study groups the post-operative pain will be treated by intravenous and peroral oxycodone and paracetamol. Monitoring and ethics: Clinical examination every hour in recovery room (oedema, temperature, cutaneous sensation, distal pulses) Continuous pressure-measurement of anterior compartment in the operated leg for 24 hours Local oxygen metabolism measured by near-infrared spectroscopy in the operated leg for 24 hours Patients will be monitored in the recovery room for 24 hours after operation. Blood tests (creatine kinase and myoglobin) will be drawn before operation, when arriving in recovery room, 6 hours and 24 hours after operation in each patient.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.50 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Supportive Care Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Inclusion Criteria: Patients with a unilateral tibial shaft fracture which needs to be operated are included. Exclusion Criteria: refusal of the patient severe, generalized atherosclerosis massive obesity marked mental retardation, dementia bilateral tibial shaft fracture polytrauma, such as head injury bleeding diathesis aortic stenosis infection at the injection site certain medications affecting bleeding sepsis hypovolemia conversion to general anaesthesia due to technical difficulties anesthesiologist has a strong opinion towards GA/RA foreign patient and marked translation difficulties
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
Active ComparatorGroup II
Active ComparatorStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location