Trials / Completed
CompletedNCT02589288
Adductor Canal Block: Continuous Infusion Versus Automatic Intermittent Bolus
Adductor Canal Block: Continuous Infusion Versus Automatic Intermittent Bolus For Postoperative Analgesia After Day-Case Anterior Cruciate Ligament Reconstruction
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 80 (actual)
- Sponsor
- ASST Gaetano Pini-CTO · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The aim of this prospective, randomized , blinded study is to compare two different infusion techniques (continuous VS intermittent automatic bolus) to assess the effects of postoperative analgesia after Day-Case anterior cruciate ligament (ACL) reconstruction.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Continuous Infusion of ropivacaine 0.2% | Postoperative continuous infusion of Ropivacaine 0,2% at 6 ml/h and 4 ml PCA bolus, lockout 20 minutes via electronic infusion pump (Micrel device, Greece). |
| PROCEDURE | Automatic Intermittent Bolus of ropivacaine 0.2% | Postoperative Automatic Intermittent Bolus of 6 ml Ropivacaine 0,2% every hour and 4 ml PCA bolus, lockout 20 minutes via electronic infusion pump (Micrel device, Greece). |
Timeline
- Start date
- 2015-11-01
- Primary completion
- 2016-12-01
- Completion
- 2017-03-01
- First posted
- 2015-10-28
- Last updated
- 2017-08-14
Locations
1 site across 1 country: Italy
Source: ClinicalTrials.gov record NCT02589288. Inclusion in this directory is not an endorsement.