Trials / Terminated
TerminatedNCT03691935
Erector Spinae Plane Block (ESPB): in Patients Undergoing Surgery Through a Flank or Anterior Subcostal Incision.
Erector Spinae Plane Block (ESPB): A New Technique for Perioperative Pain Control in Patients Undergoing Surgery Through a Flank or Anterior Subcostal Incision.
- Status
- Terminated
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 20 (actual)
- Sponsor
- Milton S. Hershey Medical Center · Academic / Other
- Sex
- All
- Age
- 18 Years – 85 Years
- Healthy volunteers
- Not accepted
Summary
Using a randomized double-blinded study design, the study goal is to evaluate the superiority of Erector Spinae Plane block (ESPB) in the peri-operative pain management of patients undergoing surgery through a flank or anterior subcostal incision as compared to the standard of care of using IV and oral opiates.
Detailed description
40 subjects will be randomized in to 2 groups, with 20 in each group. * Group 1. Erector spinae plane block (ESPB) (containing Ropivacaine) * Group 2. Sham Erector spinae plane block. (SESPB) (with normal saline)
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Ropivacaine | Erector Spinae Block with ropivacaine infusion with standard of care analgesics for perioperative pain control |
| DRUG | Normal saline | Erector Spinae Block with saline infusion with standard of care analgesics for for perioperative pain control |
Timeline
- Start date
- 2018-09-28
- Primary completion
- 2024-01-19
- Completion
- 2024-02-02
- First posted
- 2018-10-02
- Last updated
- 2025-02-10
- Results posted
- 2025-02-10
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT03691935. Inclusion in this directory is not an endorsement.