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Search / Trial NCT06088875

Nebulization Versus Spray-as-You-Go Airway Topical Anesthesia Using Dexmedetomidine and Lidocaine Mixture During Awake Flexible Fiberoptic Intubation in Temporomandibular Ankylosis

Launched by TANTA UNIVERSITY · Oct 12, 2023

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

ClinConnect Summary

This clinical trial is studying two different ways to numb the throat during a specific medical procedure called awake flexible fiberoptic intubation for patients with a condition known as temporomandibular ankylosis (TMJ ankylosis). The researchers want to find out whether using a nebulizer (a device that turns liquid medication into a mist) is more effective than a spray method for delivering a mixture of medications called dexmedetomidine and lidocaine. These medications help to make the throat numb to make the intubation process easier and more comfortable.

To participate in this study, individuals must be between 21 and 65 years old, have TMJ ankylosis, and are scheduled for surgery that requires general anesthesia. They should also be in good health according to specific medical guidelines. Participants can expect to receive one of the two methods of anesthesia during their procedure, and their comfort and the effectiveness of the anesthesia will be monitored. It's important to note that this trial is not for everyone; those with certain health conditions or allergies to the study medications cannot participate.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Age from 21to 65 years.
  • Both sexes.
  • American Society of Anesthesiologists (ASA) physical status I or II and scheduled for elective surgery requiring general anesthesia , and known to have Temporomandibular joint ankylosis and expected to be difficult intubation patient due to restriction of jaw mobility and limited mouth opening less than 2 fingers.
  • Exclusion Criteria:
  • History of allergy to dexmedetomidine or lidocaine.
  • History of drug abuse.
  • Concomitant use of medications which may exaggerate the heart rate (HR) response of -dexmedetomidine (e.g. digoxin or β-adrenergic antagonists), HR \<50 beats/min, systolic blood pressure (SBP) \<90 mmHg.
  • Pregnancy.
  • Morbid obesity( BMI more than 35).
  • Patients on anticoagulants, nasal trauma, deformity or polyp, CSF rhinorrhea, fracture base skull.
  • Cardiac and/or respiratory disease, reactive airway disease, hepatic or renal disorders.

About Tanta University

Tanta University is a prestigious academic institution located in Egypt, dedicated to advancing medical research and education. As a clinical trial sponsor, Tanta University leverages its extensive resources and expertise to conduct innovative research initiatives aimed at improving health outcomes. The university collaborates with a network of healthcare professionals, researchers, and institutions to facilitate rigorous clinical trials across various medical disciplines. Committed to ethical standards and scientific integrity, Tanta University strives to contribute to the global body of knowledge while fostering the next generation of medical professionals.

Locations

Tanta, El Gharbia, Egypt

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported