Ignite Creation Date:
2024-05-06 @ 3:54 PM
Last Modification Date:
2025-12-16 @ 5:12 PM
Study NCT ID:
NCT04797559
Status:
None
Last Update Posted:
2023-08-14 00:00:00
First Post:
2021-03-10 00:00:00
Brief Title:
SZMN Blocks for Pain Control in Pediatric Patients Undergoing T&A
Sponsor:
Stanford University
Organization:
Stanford University
Study Overview
Official Title:
Suprazygomatic Maxillary Nerve (SZMN) Blocks for Pain Control in Pediatric Patients Undergoing T&A: Randomized Controlled Trial ]
Status:
None
Status Verified Date:
2023-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
SZMN
Brief Summary:
Patients between 6 months and 18 years undergoing T\&A surgical procedures will be reviewed for potential study enrollment. If participants agree to participate, they will be randomized into either the suprazygomatic maxillary nerve (SZMN) block treatment cohort or the control cohort i.e standard of care.
After anesthesia induction, patients randomized into the SZMN- treatment group will receive a bilateral single injection SZMN block under general anesthesia in the operating room. The injection will occur near the temples above the cheek bones.
Participants enrolled into the control group will receive standard of care with no changes to their anesthetic or surgical care. Both groups will be asked for their verbal pain scores in the PACU and we will track their opioid consumption throughout the next few days after their procedure.
After anesthesia induction, patients randomized into the SZMN- treatment group will receive a bilateral single injection SZMN block under general anesthesia in the operating room. The injection will occur near the temples above the cheek bones.
Participants enrolled into the control group will receive standard of care with no changes to their anesthetic or surgical care. Both groups will be asked for their verbal pain scores in the PACU and we will track their opioid consumption throughout the next few days after their procedure.
Detailed Description:
Patients between 6 months and 18 years undergoing TA surgical procedures will be reviewed for potential study enrollment If participants agree to participate they will be randomized into either the suprazygomatic maxillary nerve SZMN block treatment cohort or the control cohort ie standard of care
After anesthesia induction patients randomized into the SZMN- treatment group will receive a bilateral single injection SZMN block under general anesthesia in the operating room The injection will occur near the temples above the cheek bones
Participants enrolled into the control group will receive standard of care with no changes to their anesthetic or surgical care Both groups will be asked for their verbal pain scores in the PACU and we will track their opioid consumption throughout the next few days after their procedure
After anesthesia induction patients randomized into the SZMN- treatment group will receive a bilateral single injection SZMN block under general anesthesia in the operating room The injection will occur near the temples above the cheek bones
Participants enrolled into the control group will receive standard of care with no changes to their anesthetic or surgical care Both groups will be asked for their verbal pain scores in the PACU and we will track their opioid consumption throughout the next few days after their procedure
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None