Ignite Creation Date:
2024-05-06 @ 10:08 AM
Last Modification Date:
2024-10-26 @ 12:25 PM
Study NCT ID:
NCT03171090
Status:
COMPLETED
Last Update Posted:
2019-10-29
First Post:
2017-05-25
Brief Title:
Efficacy of Bilateral Ultrasonic Guided Sphenopalatine Ganglion Block in Maxilofacial Cancer Surgeries
Sponsor:
Assiut University
Organization:
Assiut University
Study Overview
Official Title:
Efficacy of Bilaterally Ultrasonic Guided Sphenopalatine Ganglion Block for Perioperative Pain Management in Maxilofacial Cancer Surgeries
Status:
COMPLETED
Status Verified Date:
2019-10
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:
None
Brief Summary:
Patients will be randomly allocated according to computer - generated tables to one of two groups group A ultrasonic guided sphenopalatine block using local anasthetic group B ultrasonic guided sphenopalatine block using saline Before induction anesthesia the following will be assessed time needed to perform the technique time till onset of the block distribution of the block Opthalmic Maxillary Mandibular by needle brickIntra and post- operatively the following will be assesse the quality of operative filed every 30 min intra-operatively using a pre- defined average category scale ACS from 0 to 5 End tidal Sevo Flurane concentration will be recorded intra- operatively every 5 minutes The total amount of Nitroglycerine used to achieve the target MAP and frequency of propranolol usage will be recordedemergence time postoperative VAS score and amount of meperdine used for rescue analgesia
Detailed Description:
None
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