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Head and Neck Disorder clinical trials

View clinical trials related to Head and Neck Disorder.

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NCT ID: NCT06054178 Not yet recruiting - Clinical trials for Head and Neck Disorder

Identification of Nerves Using Fluorescein Sodium

Start date: May 2024
Phase: Phase 2
Study type: Interventional

The purpose of this study is to see if there is benefit in using an IV contrast (sodium fluorescein) called AK-Fluor® to identify nerves during head and neck surgery.

NCT ID: NCT04803032 Completed - Surgery Clinical Trials

Trident Landmark as a Safe and Easy Method for Facial Nerve Trunk Identification During Superficial Parotidectomy

Start date: January 1, 2018
Phase: N/A
Study type: Interventional

The parotid has a close relationship with the extra temporal course of the facial nerve. The study aimed to evaluate the accuracy and safety of trident landmark during superficial parotidectomy in the identification of the facial nerve trunk.

NCT ID: NCT04023474 Completed - Clinical trials for Head and Neck Disorder

Platelet-Rich Fibrin in the Healing of Regional and Free Flaps

Start date: December 16, 2019
Phase: N/A
Study type: Interventional

Determine if the use of platelet-rich fibrin (PRF) versus historical treatment methods improves the post-operative management of healing complications from flap donor sites.

NCT ID: NCT03320278 Completed - Clinical trials for Difficult Intubation

The Evaluation of Simplified Predictive Intubation Difficulty Score.

Start date: October 2016
Phase:
Study type: Observational [Patient Registry]

Difficult intubation is considered one of the most important obstacle increasing mortality in anesthesiology. Airway assessment tests are proceeded to overcome these difficulties in the pre-anesthetic evaluation. In this study, the Simplified Predictive Intubation Difficulty Score (SPIDS) and Thyromental Height Measurement (TMH) were chosen as primary methods to predict difficult intubation. The ear-nose-throat (ENT) and Plastic Surgery patients were planned to enroll this study to assess the effectiveness of these tests in predicting difficult intubation in Maltepe University Hospital and Sisli Hamidiye Etfal Governmental Hospital. The SPIDS of volunteers will be calculated according to their previous knowledge of difficult intubation, airway pathologies, head and neck movements, mouth opening, modified Mallampati test and thyromental distance. TMH value will be measured with ASIMETO depth device. Finally, the SPIDS and TMH values will be statistically compared to predict difficult intubation which is determined with difficult intubation score (IDS).

NCT ID: NCT02416752 Completed - Pain Clinical Trials

Effect of Remifentanil on the Recovery Profile After Prolonged Head and Neck Surgery

Start date: August 2011
Phase: N/A
Study type: Observational

Opioid tolerance in the perioperative period is inevitable especially with ultra-short acting agents such as remifentanil. Existing evidence had shown that opioid induced hyperalgesia due to neuroplastic changes in the central as well as peripheral nervous system leads to sensitization of pro-nociceptive pathways. However there has been a controversy of occurrence of such tolerance following the use of remifentanil and the quality of recovery as compared to conventional opioids. The investigators evaluated the occurrence of opioid tolerance and other significant adverse effects with remifentanil in subjects undergoing head and neck surgeries. The investigators studied ASA physical status I and II adult subjects undergoing elective head and neck procedures, under general anesthesia with minimum expected duration of 2 hours. The remifentanil infusion was used in one group and intermittent boluses of morphine or fentanyl administered in another group. They were evaluated for immediate post-operative pain by using numerical rating scale (NRS), the opioid consumption, post-operative nausea, vomiting, other significant adverse effects of remifentanil and the time to discharge from PACU.