Trials / Completed
CompletedNCT06087549
PENG Block vs. ESP Block for Pediatric Hip Surgery
PENG Block vs. ESP Block for Pediatric Hip Surgery. A Randomized, Prospective Double-blinded Clinical Trial.
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 90 (actual)
- Sponsor
- Poznan University of Medical Sciences · Academic / Other
- Sex
- All
- Age
- 2 Months – 12 Years
- Healthy volunteers
- Not accepted
Summary
The study compares the effectiveness and safety of the pericapsular nerve blockade vs. ESPB in pediatric patients who underwent hip surgeries.
Detailed description
The study compares the effectiveness and safety of the pericapsular nerve blockade vs. ESPB in pediatric patients who underwent hip surgeries. In addition, we aim to determine the optimal volume of local anesthetics needed to achieve a satisfactory level of analgesia.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Pericapsular nerve group block using 0.2% ropivacaine | Unilateral ultrasound guided pericapsular nerve block using 0.5mL/kg 0.2% Ropimol (max 20mL) |
| DRUG | Erector Spinae Plane Block using 0.2% ropivacaine | Unilateral ultrasound guided erector spinae block using 0.5mL/kg 0.2% Ropimol (max 20mL) |
| OTHER | Standard care | No erector spinae block and no pericapsular nerve group block |
Timeline
- Start date
- 2023-10-17
- Primary completion
- 2024-02-23
- Completion
- 2024-02-23
- First posted
- 2023-10-17
- Last updated
- 2024-02-28
Locations
1 site across 1 country: Poland
Source: ClinicalTrials.gov record NCT06087549. Inclusion in this directory is not an endorsement.