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NCT04567407 · ClinicalTrials.gov registry record · Phase 4
Bilateral Continuous Erector Spinae Blocks for Post-Sternotomy Pain Management
A Phase 4 study, sponsored by Boston Children's Hospital.
- Completed
- Registry status
- Phase 4
- Development phase
- 45
- Enrollment target
NCT04567407 is a Phase 4 study that has completed, run by Boston Children's Hospital. The registered enrollment target is 45 participants.
The verdict
NCT04567407, a Phase 4 study, has completed, sponsored by Boston Children's Hospital.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 45 participants
- Enrollment target
Study Summary
To evaluate the efficacy of bilateral continuous erector spinae blocks (BESB) for postoperative analgesia in children and adolescents undergoing cardiac surgical procedures via sternotomy in the Early Recovery After Surgery (ERAS) program in a single arm, open label, interventional study.
Interventions
- DRUG Bilateral erector spinae blocks using ropivacaine
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 45 participants |
| Start Date | 2020-09-22 |
| Est. Completion | 2022-01-22 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04567407
The ClinicalTrials.gov registry entry for NCT04567407 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 45 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Boston Children's Hospital, which has 462 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Bilateral erector spinae blocks using ropivacaine is the first listed.
NCT04567407 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT04567407 about?
NCT04567407 is a clinical study titled "Bilateral Continuous Erector Spinae Blocks for Post-Sternotomy Pain Management". To evaluate the efficacy of bilateral continuous erector spinae blocks (BESB) for postoperative analgesia in children and adolescents undergoing cardiac surgical procedures via sternotomy in the Early Recovery After Surgery (ERAS) program in a single arm, open label, interventional study.
What is the current status of trial NCT04567407?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 45 participants. The study started on 2020-09-22. Estimated completion is 2022-01-22.
What interventions are being tested in trial NCT04567407?
The interventions under investigation include: Bilateral erector spinae blocks using ropivacaine (DRUG).
Who is sponsoring clinical trial NCT04567407?
This trial is sponsored by Boston Children's Hospital, which has 462 total clinical trials registered on ClinicalTrials.gov.
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