None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: * ASA physical status 1-3 * Age: 19-80 years * Patients with brachial plexus block and scheduled upper extremity surgery under supervised general anesthesia
Exclusion criteria
Exclusion criteria: * Informed Consent Refusers * Pregnancy * Any contraindication to axillary brachial plexus block (Any contraindication to axillary BPB) * Pre-existing neuropathy involving the surgical limb (Pre-existing neuropathy involving the surgical limb) * systemic use of corticosteroids for 2 weeks or longer within 6 months of surgery (systemic use of corticosteroids for 2 weeks or longer within 6 months of surgery) * Allergy to any medication included in the study protocol, including ropivacaine. Translated with DeepL.com (free version)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| sensory block duration ;motor block duration | — |
Secondary
| Measure | Time frame |
|---|---|
| Time to first analgesic intake after axillary brachial plexus block;Analgesic consumption 24 and 48 hours after surgery;QoR-15 (Quality of recovery-15);Pain score at 8, 24, and 48 hours after surgery (NRS score);Patient satisfaction (7-point Likert’s scale);Quantity and quality of sleep on the day of surgery (numerical rating scale for sleep); Complications related to postoperative nerve block procedure (general local anesthesia toxicity, paresthesia or nerve damage);Complications due to dexamethasone administration (infection or increased blood sugar) | — |
Countries
Korea, Republic of
Contacts
Asan Medical Center