Trials / Completed
CompletedNCT05834023
Bupivacaine Versus Bupivacaine Plus Lidocaine in Infraclavicular Block
Comparison Between Bupivacaine 0.5% Versus Bupivacaine 0.25% Plus Lidocaine 1% in Ultrasound-guided Infraclavicular Block: a Prospective Randomized Controlled Trial
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 40 (actual)
- Sponsor
- Hospital de San Carlos Dr. Benicio Arzola Medina · Academic / Other
- Sex
- All
- Age
- 18 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
In this study, the investigators will compare two different anesthetic solutions in the infraclavicular block in patients having forearm, wrist, and hand surgery. The solutions will be bupivacaine 0.5% versus bupivacaine 0.25% plus lidocaine 1%, both associated with epinephrine 5 mcg/ml and dexamethasone 4 mg. The main objective of this investigation is to demonstrate that using higher concentrations of bupivacaine alone results in a significant block duration increase compared with the mixture of bupivacaine and lidocaine.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Bupivacaine-Lidocaine | Infraclavicular block with 35 ml of the following anesthetic solution: Bupivacaine 0.25% + Lidocaine 1% + dexamethasone 4 mg + epinephrine 5 mcg/ml |
| DRUG | Bupivacaine | Infraclavicular block with 35 ml of the following anesthetic solution: Bupivacaine 0.5% + dexamethasone 4 mg + epinephrine 5 mcg/ml |
Timeline
- Start date
- 2023-05-02
- Primary completion
- 2023-12-29
- Completion
- 2024-01-05
- First posted
- 2023-04-27
- Last updated
- 2024-01-17
Locations
1 site across 1 country: Chile
Source: ClinicalTrials.gov record NCT05834023. Inclusion in this directory is not an endorsement.