Clinical Trials Directory

Trials / Completed

CompletedNCT03047070

Lidocaine in ERAS for FESS

Lidocaine Infusion in Functional Endoscopic Sinus Surgery

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
43 (actual)
Sponsor
Assiut University · Academic / Other
Sex
All
Age
20 Years – 50 Years
Healthy volunteers
Not accepted

Summary

Functional endoscopic sinus surgery (FESS) is a commonly performed procedure. It is known that bleeding during FESS can affect directly to the visibility of safe landmarks and surgical outcomes.

Detailed description

Functional endoscopic sinus surgery (FESS) is a commonly performed procedure in the head and neck field. It is known that bleeding during FESS can affect directly to the visibility of safe landmarks and surgical outcomes. Use of vasoactive drugs to control bleeding is not without pitfalls. Systemic effects of epinephrine may constitute a potential hazard in patients with hypertension, ischemic heart disease, anemia, preexistent liver or renal damage and endocrine dysfunction (hyperthyroidism, pheochromocytoma and diabetes mellitus). Lidocaine is a prototypical local anesthetic, but it also has systemic effects that are mediated by inhibitory effects on N-methyl-d-aspartate receptors and leukocyte priming. Consequently, systemic lidocaine is antiinflammatory, analgesic, and antihyperalgesic. Randomized clinical trials, however, have produced mixed results. Several studies have shown reduction in postoperative opioid consumption and pain scores, whereas others have failed to show a benefit.

Conditions

Interventions

TypeNameDescription
DRUGLidocaineIV Lidocaine infusion
DRUGNormal salineIV normal saline infusion

Timeline

Start date
2017-02-09
Primary completion
2021-12-31
Completion
2021-12-31
First posted
2017-02-08
Last updated
2022-04-28

Locations

2 sites across 1 country: Egypt

Source: ClinicalTrials.gov record NCT03047070. Inclusion in this directory is not an endorsement.