Sphenopalatine Ganglion Block for Nasal Surery

Postoperative Delirium Clinical Trial

Official title:

Efficacy of Suprazygomatic Approach of Sphenopalatine Ganglion Block for Nasal Surery

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04168879
• Other study ID #: ACCA
• Status: Completed
• Phase: N/A
• Start date: November 10, 2021
• Est. completion date: December 10, 2023

Study information

• Verified date: May 2024
• Source: Assiut University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

nasal surgery carries many perioperative challenges, intraoperative bleeing and its effect on surgical field i the main intraoperative concern an postoperative agitation and its serious complications is the main postoperative challenge.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 108
• Est. completion date: December 10, 2023
• Est. primary completion date: December 10, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 55 Years

Eligibility

Inclusion Criteria:

• patient written consent
• elective surgery
• age 18 - 55 year old

Exclusion Criteria:

• patient refusal
• emergency surgery

Related Conditions & MeSH terms

• Emergence Delirium
• Postoperative Delirium

Intervention

Drug:
• Bupivacaine 0.5% Preservative-Free Injectable Solution
1.5 ml of Bupivacaine 0.5% Preservative-Free Injectable Solution used to block the sphenopalatine ganglion by ultrasound guided suprazygomatic approach
• normal saline
1.5 ml of normal saline is delivered to the sphenopalatine ganglion by ultrasound guided suprazygomatic approach

Locations

Country	Name	City	State
Egypt	Faculty of Medicine	Asyut

Sponsors (2)

Lead Sponsor	Collaborator
Assiut University	saeid metwaly abouelyazid elsawy

Country where clinical trial is conducted

Egypt, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	intraoperative bleeding	suction and weight of surgical gauze used was measured and calculated	2 hours
Primary	Postoperative emergence agitation	ramsy hunt sedation agitation score used during emergence from anesthesia	2 hour
Secondary	postoperative opioid consumption	total amount of opioid analgesia in first 24 hours postoperative	24 hour
Secondary	surgical field quality	Boezaart score was be used	2 hours
Secondary	consumed inhalational anesthesia	mean anesthesia MAC intraoperative	2 hours
Secondary	postoperative pain	using VAS ; scale from 0 to 10 . where 0 is no pain and 10 is worst pain	2 hours