Trials / Completed
CompletedNCT06427551
Volume Effect in Peng Block for Total Hip Replacement
Peng Block in Total Hip Replacement: Effects of Anesthetic Volume on Clinical Outcome and Postoperative Complications
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 120 (actual)
- Sponsor
- Azienda Ospedaliero, Universitaria Pisana · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This study is to investigate whether a different volume of ropivacaine, with the same prescribed dosage based on body weight, can affect block efficacy, duration and side effects in the first 24 hours postoperatively.
Detailed description
patients were divided into 3 groups on the basis of the volume of anesthetic given to perform the block. in every patient was assessed the nrs, the side effects, if any, and the need for analgesic drugs in the first 24 hour after surgery
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Ropivacaine | The local anesthetic was dosed on the patient's weight (50-59kg: 120mg, 60-61kg: 140mg, 70-79kg: 160mg, ≥80kg: 180mg) |
Timeline
- Start date
- 2022-01-01
- Primary completion
- 2024-01-30
- Completion
- 2024-01-30
- First posted
- 2024-05-24
- Last updated
- 2024-05-24
Locations
1 site across 1 country: Italy
Source: ClinicalTrials.gov record NCT06427551. Inclusion in this directory is not an endorsement.