Ultrasonography Clinical Trial
Official title:
Midline Versus Paramedian Approaches for Ultrasound-assisted Spinal Anesthesia: a Randomized Controlled Trial
Verified date | December 2019 |
Source | Seoul National University Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Ultrasound has emerged as an useful tool for neuraxial blockade. The aim of this study is to compare the efficacy and safety between the midline approach and paramedian approach for ultrasound-assisted spinal anesthesia in adult patients.
Status | Completed |
Enrollment | 112 |
Est. completion date | October 9, 2018 |
Est. primary completion date | October 8, 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Adult patients scheduled to undergoing elective orthopedic surgery under spinal anesthesia, with ASA physical status classification I, II, III Exclusion Criteria: - Patients with contraindication to spinal anesthesia (coagulopathy, local infection, allergy to local anesthetic) - Patients with morbid cardiac diseases - Pregnancy - Patients with previous history of lumbar spinal surgery - Patients with anatomical abnormality of lumbar spine |
Country | Name | City | State |
---|---|---|---|
Korea, Republic of | Seoul National University Hospital | Seoul |
Lead Sponsor | Collaborator |
---|---|
Seoul National University Hospital |
Korea, Republic of,
Kallidaikurichi Srinivasan K, Iohom G, Loughnane F, Lee PJ. Conventional Landmark-Guided Midline Versus Preprocedure Ultrasound-Guided Paramedian Techniques in Spinal Anesthesia. Anesth Analg. 2015 Oct;121(4):1089-96. doi: 10.1213/ANE.0000000000000911. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | the number of needle passes | the number of forward advancements of the spinal needle in a given interspinous space, i.e., withdrawal and redirection of spinal needle without exiting the skin | Intraoperative (from the first insertion of needle to patient's skin, until the completion of spinal anesthetic injection) | |
Secondary | Number of spinal needle insertion attempts | the number of times the spinal needle was withdrawn from the skin and reinserted | Intraoperative (from the first insertion of needle to patient's skin, until the completion of spinal anesthetic injection) | |
Secondary | Time for identifying landmarks | time from placement of the ultrasound probe on the skin to the completion of markings. | intraoperative (time taken for establish the landmark, from start of US scanning to completion of scanning | |
Secondary | Time taken for performing spinal anesthetic | time from needle insertion to the completion of injection | Intraoperative (from insertion of the needle to the completion of injection) | |
Secondary | dermatome level of sensory block | thoracic dermatome level of sensory block assessed by loss of cold sensation tested with 2% chlorhexidine swab | 20 minutes after the completion of spinal anesthetic injection | |
Secondary | Incidence of radicular pain, paraesthesia, and blood tapping in the spinal needle | Incidence of radicular pain, paraesthesia, and blood tapping in the spinal needle during the spinal anesthesia procedure | Intraoperative (from the first insertion of needle, until the completion of spinal anesthetic injection) | |
Secondary | Periprocedural pain | 11-point verbal rating scale (0=no pain, 10=most pain imaginable) | Patients will be asked immediately after the completion of spinal anesthesia | |
Secondary | Periprocedural discomfort score | 11-point verbal rating scale (0=no discomfort, 10=most discomfort imaginable) | Patients will be asked immediately after the completion of spinal anesthesia | |
Secondary | Patient satisfaction score of spinal anesthesia procedure | 11-point verbal rating scale (0=very unsatisfied, 10=very satisfied) | Patients will be asked immediately after the completion of spinal anesthesia |
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