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Thyroid Diseases clinical trials

View clinical trials related to Thyroid Diseases.

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NCT ID: NCT04879355 Recruiting - Thyroid Nodule Clinical Trials

Spinal Needles in Ultrasound-guided Fine Needle Aspirations From Thyroid Nodules

Start date: November 1, 2021
Phase: N/A
Study type: Interventional

This is a multicentre, two-arm, randomised and controlled trial. Adults with thyroid nodules suspected of malignancy are to be included consecutively. A total of 350 patients are randomly assigned 1:1 to have FNA with a spinal (25G) or a conventional (25G) needle. The primary outcome is the rate of diagnostic cytological samples according to the Bethesda system. Secondary outcomes are diagnostic accuracy, patient's experienced pain and complication rates.

NCT ID: NCT04873531 Completed - Thyroid Diseases Clinical Trials

Feasibility of Neostigmine for Intraoperative Neuromonitoring in Thyroid Surgery

Start date: May 10, 2021
Phase: N/A
Study type: Interventional

For successful intraoperative neuromonitoring (IONM), adequate reversal of neuromuscular blocking agent is a prerequisite in thyroid surgery with . The aim of this study is to investigate the feasibility of neostigmine just after tracheal intubation on the IONM in thyroid surgery.

NCT ID: NCT04868045 Withdrawn - Thyroid Cancer Clinical Trials

Study of Resistance to Thyroid Hormone After Long-term Exposure in People With Thyroid Cancer

Start date: April 27, 2021
Phase: Phase 1
Study type: Interventional

The purpose of this study is to find out whether people who have had thyroid cancer develop resistance to treatment with thyroid hormones after having received high doses of thyroid drugs for many years.

NCT ID: NCT04857086 Recruiting - Clinical trials for Differentiated Thyroid Cancer

The Initial Management in Patients With Differentiated Thyroid Cancer in the Real World in China

Start date: December 30, 2020
Phase:
Study type: Observational

- To find out the gap between real-world clinical practice and guideline recommendations in initial management of DTC patients - To observe the characteristics of patients who achieved and did not achieve TSH target value after five year follow-up - To assess response to initial therapy in patients who undergo total or neartotal thyroidectomy and RAI remnant ablation after five year follow-up (according to an modified dynamic risk stratification system) - To observe the recurrence status after five year follow-up

NCT ID: NCT04853680 Recruiting - Thyroid Cancer Clinical Trials

Effect of Anti-adhesion Barrier on the Voice Quality After Thyroidectomy.

Start date: July 1, 2021
Phase: N/A
Study type: Interventional

To determine whether the use of anti-adhesion barrier after thyroid surgery can prevent the voice changes after surgery, using objective voice-related indicators.

NCT ID: NCT04845867 Not yet recruiting - Thyroid Clinical Trials

Thyroid HEmorrhage DetectOr Study

HEDOS
Start date: July 1, 2021
Phase:
Study type: Observational [Patient Registry]

After thyroid surgery, 0.6 to 4% of patients develop postoperative bleeding. 90% of this postoperative bleeding occurs within the first 48 hours. Most of the time, the complications are rapidly progressing and require immediate attention. Up to 0.6% of patients with postoperative bleeding die. In a clinical study with postoperative pressure measurements it could be shown that postoperative bleeding without interruption leads to a continuous increase in pressure in the neck, as is observed when coughing and pressing. Systematic invasive pressure measurement in the thyroid compartment after surgery might detect a continuous increase in pressure which is often caused by a growing haematoma, indicating serious post-surgery bleeding at a much earlier time compared to state of the art diagnostic workflow. n routine clinical care, detection of serious haemorrhage depends on the patients alerting symptoms even if post-operative intermittent monitoring of vital parameters and wound conditions is performed according to current medical guidelines [18] and local instructions. Device-based, continuous haemorrhage detection within 36 to 48 hours after surgery would allow to objectively measure an increase in cervical pressure before symptoms occur, i.e. early detection of risk leading to timely therapeutic actions. Thus, the risk of serious complications like hypoxic brain damage and death caused by post-operative haemorrhage is minimized. In addition, the intervention team would be able to fine-tune necessary actions during the rescue procedure based on objective pressure values, e.g. the decision to open cutaneous sutures immediately or later in the operation theatre, and therefore reduce additional perioperative morbidity and increase patients' safety.

NCT ID: NCT04842994 Recruiting - Clinical trials for Malignant Neoplasm of Thyroid Gland

Trial on Intraoperative Neuromonitoring (IONM) in Thyroid Cancer Surgery.

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

Scientific objectives: Primary objective: • To assess if the use of IONM can decrease the rates of temporary RLN palsy after thyroid cancer surgery Secondary objectives: - To assess if the use of IONM can decrease permanent RLN palsy rates in patients with thyroid cancers - To assess voice parameters in patients with RLN palsy Methodology: All patients undergoing total thyroidectomy with or without central compartment neck dissection, for thyroid cancers, will be eligible for participation. After confirmation of eligibility and obtaining informed consent, all patients will undergo preoperative screening procedures. Fibreoptic laryngoscopy (FOL) examination will be done to document function of the vocal cords. Preoperative voiceevaluation, GRBAS voice scale assessment and Voice Related Quality of Life (VR-QOL) assessment will be performed for all patients. Patients will then be randomized in a 1:1 ratio to receive IONM or not during surgery. Patients will be stratified as per predefined stratification factors. After surgery, endpoint assessment of vocal cord mobility will be done with a FOL study, by an assessor blinded to the randomization arm. Voice evaluation, GRBAS scale assessment and VR QOL assessment will also be done. An event will be defined as any vocal fold paresis/palsy. Patients without the event will be followed up for 6 months while patients with the event will be followed up for 2 years to assess recovery of vocal cord function and changes in speech parameters. All patients with vocal cord paresis/palsy will be given speech and swallowing rehabilitation

NCT ID: NCT04842942 Recruiting - Surgery Clinical Trials

The Safety and Feasibility of Transoral Endoscopic Thyroidectomy Vestibular Approach

Start date: December 1, 2019
Phase: Phase 1
Study type: Interventional

This is a single center, prospective case series designed to assess the safety and feasibility of TOETVA in a small cohort of patients at University Health Network Toronto. Included patients will undergo a TOETVA-procedure in stead of the standard open surgical procedure.

NCT ID: NCT04821336 Completed - Thyroid Cancer Clinical Trials

Cholesterol Metabolites Analysis in Human Thyroid and Iodine Resistance

OXYTHYR
Start date: April 15, 2021
Phase:
Study type: Observational

The study team previously shown that a cholesterol metabolite, dendrogenin A (DDA) differentiates anaplastic thyroid cancer cell lines and that its mRNA expression is diminished in human radioiodine refractory thyroid cancer samples. The team aim to quantify via mass spectrometry and immunohistochemistry DDA and other cholesterol metabolites in thyroid cancer versus healthy thyroid tissue human samples.

NCT ID: NCT04794257 Recruiting - Surgery Clinical Trials

NerveTrend vs. i-IONM in Prevention of Recurrent Laryngeal Nerve Events During Bilateral Thyroid Surgery.

Start date: April 1, 2021
Phase: N/A
Study type: Interventional

The aim of this study is to compare two distinct modes of NIM Vital application in thyroid surgery: i-IONM vs. NerveTrend mode with respect to prevalence of early postoperative RLN injury. The hypothesis explored in this study is that NerveTrend mode may be more accurate than conventional i-IONM mode in intraoperative identification of impending neural injury and in prognostication of postoperative glottis function in monitored bilateral thyroid surgery. Hence, NerveTrend mode may be considered a bridge between i-IONM and c-IONM modes, and particularly in health care environments with limited financial resources it can be considered a substantial step forward representing a modern alternative to the c-IONM technique and providing benefits over conventional i-IONM mode. A prospective, randomized study with 2 arms: i-IONM vs. NeveTrend mode (n=132 patients and 264 nerves at risk, each). The primary outcome measure is prevalence of recurrent laryngeal nerve (RLN) injury (%) on postoperative day 1 assessed by direct laryngoscopy.