Effect of Fentanyl With Topical Levobupivacaine With Nasal Packing in Endoscopic Nasal Surgery

Analgesia During Removal of Nasal Pack After Nasal Surgery Clinical Trial

— fentanyl  

Official title:

Effect of Fentanyl With Topical Levobupivacaine With Nasal Packing in Endoscopic Nasal Surgery

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04410588
• Other study ID #: marwawael
• Status: Recruiting
• Phase: Phase 2
• Start date: June 20, 2020
• Est. completion date: August 2021

Study information

• Verified date: July 2021
• Source: Assiut University
• Contact: Marwa M Abdelrady
• Phone: 01006805857
• Email: marwarady-2012[@]hotmail.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

the Investigators aim to study the effect of fentanyl with topical levobupivacaine with nasal packing in endoscopic nasal surgery

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 75
• Est. completion date: August 2021
• Est. primary completion date: July 1, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 60 Years

Eligibility

Inclusion Criteria:1. All patients in the age of 18-60 year 2. ASA I-II 3. Undergoing elective nasal endoscopic surgery

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Exclusion Criteria:

1. Patients will also be excluded if any perioperative cardiovascular or respiratory event occurred which the anaesthetist with clinical responsibility for the patient thought would make the study intervention clinically unacceptable.

2. unsatisfactory preoperative peripheral arterial oxygen saturation.

3. Unsatisfactory preoperative hemoglobin level.

4. Neurological or psychiatric disease.

Related Conditions & MeSH terms

• Analgesia During Removal of Nasal Pack After Nasal Surgery

Intervention

Drug:
• Fentanyl + Topical Levobupivacaine
in nasal packing
• levobupivacaine
in nasal packing

Locations

Country	Name	City	State
Egypt	Wael	Assiut	Asyut

Sponsors (1)

Lead Sponsor	Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	postoperative pain by visual analoge score	assessment of pain on removal of nasal packing after endoscopic nasal surgery by VAS score. The Visual Analogue Scale (VAS) (0, no discomfort and no pain; 10, a high level of discomfort and maximum pain)	24 houres postoperative pain assessment