Trials / Completed
CompletedNCT04306133
PENG Block Combined to Wound Infiltration for Hip Replacement
Pericapsular Nerve Group (PENG) Block Combined to Wound Infiltration vs. Wound Infiltration Alone for Postoperative Analgesia After Total Hip Replacement: a Prospective Controlled Trial
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 60 (actual)
- Sponsor
- Campus Bio-Medico University · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This study analyze the effect of Pericapsular Nerve Group (PENG) Block combined to wound infiltration for analgesia after elective hip replacement. Half of participants will receive a PENG Block combined with wound infiltration, while the other half will receive wound infiltration alone.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | PENG block | After performing spinal anesthesia, PENG block with 20 mL of 0.375 % Ropivacaine will be executed as described by Giron-Arongo et al with a low frequency curvilinear probe. A 22G 80 mm needle (Stimuplex Ultra 360, Braun ) will be used. |
| PROCEDURE | Wound Infiltration | At the end of operation, the surgeon will perform wound infiltration with 20 mL of 0.375 % Ropivacaine. |
Timeline
- Start date
- 2020-03-09
- Primary completion
- 2020-12-24
- Completion
- 2020-12-31
- First posted
- 2020-03-12
- Last updated
- 2021-04-06
Locations
1 site across 1 country: Italy
Source: ClinicalTrials.gov record NCT04306133. Inclusion in this directory is not an endorsement.