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NCT04909619 · ClinicalTrials.gov registry record · NA
Suprazygomatic Maxillary Nerve Block in Cleft Palate Outcomes
A NA study, sponsored by Ann & Robert H Lurie Children's Hospital of Chicago.
- Completed
- Registry status
- NA
- Development phase
- 40
- Enrollment target
NCT04909619 is a NA study that has completed, run by Ann & Robert H Lurie Children's Hospital of Chicago. The registered enrollment target is 40 participants.
The verdict
NCT04909619, a NA study, has completed, sponsored by Ann & Robert H Lurie Children's Hospital of Chicago.
- COMPLETED
- Registry status
- NA
- Development phase
- 40 participants
- Enrollment target
Study Summary
Increased pain after cleft palate surgery is the leading cause of increased hospital length of stay, delayed oral intake, readmission, and respiratory compromise. The goal is to improve all outcomes by identifying the most effective evidenced-based method of intra-operative pain control.
Interventions
- PROCEDURE Ultrasound-guided bilateral suprazygomatic maxillary nerve block
- PROCEDURE Local anesthetic infiltration of the palate
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 40 participants |
| Start Date | 2021-03-01 |
| Est. Completion | 2025-06-30 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04909619
The ClinicalTrials.gov registry entry for NCT04909619 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Ann & Robert H Lurie Children's Hospital of Chicago, which has 159 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Ultrasound-guided bilateral suprazygomatic maxillary nerve block is the first listed.
NCT04909619 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT04909619 about?
NCT04909619 is a clinical study titled "Suprazygomatic Maxillary Nerve Block in Cleft Palate Outcomes". Increased pain after cleft palate surgery is the leading cause of increased hospital length of stay, delayed oral intake, readmission, and respiratory compromise. The goal is to improve all outcomes by identifying the most effective evidenced-based method of intra-operative pain control.
What is the current status of trial NCT04909619?
This trial is currently completed. It is a NA study. The enrollment target is 40 participants. The study started on 2021-03-01. Estimated completion is 2025-06-30.
What interventions are being tested in trial NCT04909619?
The interventions under investigation include: Ultrasound-guided bilateral suprazygomatic maxillary nerve block (PROCEDURE), Local anesthetic infiltration of the palate (PROCEDURE).
Who is sponsoring clinical trial NCT04909619?
This trial is sponsored by Ann & Robert H Lurie Children's Hospital of Chicago, which has 159 total clinical trials registered on ClinicalTrials.gov.
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