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Vocal Cord Paralysis clinical trials

View clinical trials related to Vocal Cord Paralysis.

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NCT ID: NCT05747859 Completed - Vocal Fold Palsy Clinical Trials

Voice Telerehabilitation

Start date: November 5, 2021
Phase:
Study type: Observational

The aim of the study was to determine functional results of telerehabilitation (TR) in subjects affected by iatrogenic unilateral vocal fold paralysis (UVFP) during the COVID-19 pandemic outbreak. 40 patients with iatrogenic unilateral vocal fold paralysis underwent voice teletherapy with a synchronous approach. A multidimensional assessment by means of videolaryngostroboscopy, acoustic and perceptual analysis and patient self-assessment was carried out before, at the end of teletherapy and six months later.

NCT ID: NCT05285423 Completed - Clinical trials for Bilateral Vocal Cord Paralysis

A Novel Approach for VC Lateralization, With Prolene Suture Stabilized Over Prolene Mesh

Start date: January 1, 2022
Phase: N/A
Study type: Interventional

The larynx performs important functions of the aero-digestive tract, it has a vital role in the control of breathing, phonation, deglutition, and protection of the lower respiratory tract from aspiration. Bilateral Vocal cord paralysis is a challenging and at times debilitating laryngeal dysfunction that has a great social and economic impact on a patient's life. VC Lateralization, if done accurately and up to the expectations of the patient is very rewarding. However different surgical procedures which include cordectomy, arytenoidectomy with or without laser, open surgical methods, and Isshiki type 2 thyroplasty are in practice. Each has its own profile of benefits and disadvantages. Most of them are technically difficult and complex, need specialized equipment, and are out of reach of the general ENT surgeons. The investigator suggests using the Prolene suture stabilized over Prolene mesh for Vocal Cord Lateralization.

NCT ID: NCT04986592 Completed - Clinical trials for Recurrent Laryngeal Nerve Palsy

Predisection Risk Factors for Vocal Cord Palsy After Total Thyroid Surgery

Start date: April 2014
Phase:
Study type: Observational [Patient Registry]

In patients undergoing total thyroidectomy, intraoperative nerve monitoring according to the International Standards Guideline Statement may detect nerves more susceptible to injury. The aim of our study was to evaluate the independent risk factors of vocal cord palsy, including those related to pre-dissection nerve monitoring values. Methods: Prospective observational study in 95 consecutive adult patients undergoing elective total thyroidectomy in Spain. A single experienced phonologist performed a videostroboscopy (VS) exam preoperatively and one week after surgery to assess vocal cord mobility. Each surgical procedure was performed with intermittent intraoperative neuromonitoring. Latency and amplitude values were obtained for the vagal and recurrent laryngeal nerves before surgical dissection and compared with the postoperative VS exam.

NCT ID: NCT04839276 Completed - Clinical trials for Vocal Cord Paralysis

Administration of Platelet-rich Fibrin to Autologous Fat Tissue in Injection Laryngoplasty for Vocal Cord Paralysis

Start date: January 1, 2018
Phase: Phase 4
Study type: Interventional

The study tries to see the effect of using a combination of platelet-rich fibrin (PRF) and autologous fat as a filler for injection laryngoplasty procedures to treat unilateral adductor vocal cord paralysis.

NCT ID: NCT04764604 Completed - Dysphonia Clinical Trials

Evaluating the Feasibility of Acapella® Choice as a Dysphonia Treatment

Start date: December 14, 2020
Phase: N/A
Study type: Interventional

A feasibility study to identify the immediate effect on the voices of patients with voice disorders (muscle tension dysphonia, vocal fold palsy or presbylaryngis) produced by exercising with Acapella Choice as a form of semioccluded vocal tract exercise (SOVTE).

NCT ID: NCT04458818 Completed - Clinical trials for Vocal Cord Paralysis

A Novel Approach for Thyroplasty Type 1, With Prolene Mesh. A Prospective Study.

Start date: May 1, 2020
Phase: N/A
Study type: Interventional

Larynx performs important functions of the aero-digestive tract, it has vital role in control of breathing, phonation, deglutition and protection of lower respiratory tract from aspiration. Vocal cord paralysis is a common and at times debilitating laryngeal dysfunction that has great social and economic impact on patients life. Medialization thyroplasty (MT), if done accurately and up to the expectations of the patient is very rewarding. However different materials with some modifications in the technique of the classical Isshiki type 1 thyroplasty is in practice, each with its own profile of benefits and disadvantages. Most of them are costly and out of reach of general population. In this regard, we aim to test a prolene mesh implant, which is easily available and can be placed with relative ease.

NCT ID: NCT04315415 Completed - Clinical trials for Vocal Cord Paralysis

A Histological Study Evaluating Silk Voice and Crosslinked Hyaluronic Acid

Start date: January 15, 2020
Phase: N/A
Study type: Interventional

The primary study goal is to evaluate the histological characteristic of Silk Voice to evaluate the potential for Silk Voice to deliver long-term results to patients.

NCT ID: NCT03966183 Completed - Clinical trials for Unilateral Vocal Cord Paralysis

Early UVFP Management Based on Neurological Evidences (ION-UVFP) - Preliminary Study

Start date: June 15, 2019
Phase:
Study type: Observational [Patient Registry]

The purpose of this preliminary study is to help clarify our hypotheses for the longitudinal study by investigating the relationship between vocal cord paralysis and central auditory processes and thus the interpretation of auditory inputs into the central nervous system.

NCT ID: NCT03906877 Completed - Clinical trials for Unilateral Vocal Cord Paralysis

Early UVFP Management Based on Neurological Evidences (UVFP = Unilateral Vocal Fold Paralysis)

IONS-UVFP
Start date: November 15, 2019
Phase: N/A
Study type: Interventional

The aim of this study is to understand how early intervention could impact reinnervation of the recurrent laryngeal nerve (which innervates the vocal cord), recovery of mobility of the paralyzed vocal cord and / or vocal recovery in the case of unilateral vocal fold paralysis. To achieve this goal we must therefore carry out a complete outcomes assessment of different intervention methods (voice therapy and injection laryngoplasty), which are offered to UVFP (unilateral vocal fold paralysis) patients in the early stage (< 3 months). Their respective impacts on the central and peripheral nervous system and on the voice quality will be assessed, taking into account factors related to the severity of the paralysis.

NCT ID: NCT03882450 Completed - Dysphagia Clinical Trials

Universal Screening for Vocal Fold Motion Impairment in Children Undergoing Congenital Cardiac Surgery

Start date: January 1, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to determine how often heart or chest surgery in children leads to problems with the movement of the vocal folds.