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Thyroidectomy clinical trials

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NCT ID: NCT02377882 Completed - THYROIDECTOMY Clinical Trials

The Optimal Dosage of Rocuronium for Intraoperative Neuromonitoring During Thyroid Surgery

IONM
Start date: January 2009
Phase: N/A
Study type: Observational

The investigators tried to explore an alternative non-depolarizing muscle relaxant (rocuronium) and its optimal dosage to replace succinylcholine for IONM during thyroid surgery.Time frame of outcome measure was during 30 to 70min after rocuronium injection. Specific time points at which the will be assessed and for EMG signals will be presented.

NCT ID: NCT02208505 Completed - Thyroidectomy Clinical Trials

Antitussive Effect of Single-dose Dexmedetomidine With Low-dose Remifentanil Infusion

Start date: February 2014
Phase: Phase 4
Study type: Interventional

After thyroid surgery, the incidence and severity of coughing is important because it may cause serious complications, such as bleeding in the surgical field, laryngospasm, and cardiovascular disturbance. Several studies have shown that the single-dose of dexmedetomidine is effective for reducing cough and agitation during emergence from general anesthesia. To test the hypothesis that single-dose of dexmedetomidine combined with a low-dose remifentanil infusion during emergence from general anaesthesia could reduce coughing as good as high-dose remifentanil infusion, we will evaluate the efficacy on cough suppression and reduction of side effect of remifentanil using non-inferiority trial.

NCT ID: NCT02136459 Completed - Thyroidectomy Clinical Trials

Non-neural Vocal Changes After Thyroidectomy

Start date: October 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to test the investigators hypothesis that intubation with a smaller ETT would lead to reduced postoperative vocal impairment and laryngoscopic evidence of laryngeal trauma than intubation with a standard size ETT.

NCT ID: NCT02122367 Recruiting - Thyroidectomy Clinical Trials

Study of Stroke Volume Variation and Pleth Variability Index as Predictors of Fluid Responsiveness

Start date: April 2014
Phase: Phase 4
Study type: Interventional

Appropriate indices to guide fluid therapy are essential for effective hemodynamic management during the perioperative period. Values derived from respiratory changes in arterial pressure waveform or plethysmographic waveform such as stroke volume variation and pleth variability index have been demonstrated to be able to predict fluid responsiveness in surgical or critically ill patients. Their ability to predict fluid responsiveness can be affected by factors that influence the arterial tone or the compliance of the respiratory system by position change. The aim of this prospective trial is to investigate the ability of stroke volume variation and pleth variability index to predict fluid responsiveness in the reverse trendelenberg position.

NCT ID: NCT01801033 Withdrawn - Hypothyroidism Clinical Trials

Effects of Thyroid Hormone Enzyme Blocking on Hypothyroidism

Start date: January 4, 2013
Phase: N/A
Study type: Observational

Background: - Hypothyroidism is a condition caused by the loss of function of the thyroid gland. The thyroid gland produces two hormones, T4 and T3. These hormones control the metabolism and function of many organs. Lack of energy, depression, and constipation are common symptoms of hypothyroidism. T4 is converted into T3, the active form of thyroid hormone, by two enzymes called deiodinases. People with hypothyroidism are treated with a synthetic T4 hormone, which the enzymes convert to T3. This treatment is usually effective, but some people continue to have symptoms even after treatment. Some researchers think that this may be caused by a problem with the enzymes that convert T4 into T3. They want to look at how the enzymes regulate the levels of T4 and T3 in the blood. They will do so by using a drug that blocks the action of one of the two enzymes. Objectives: - To look at how thyroid hormone enzyme blocking affects hypothyroidism treatment medication. Eligibility: - Individuals at least 18 years of age who have hypothyroidism and are on thyroid hormone replacement therapy. Design: - The study consists of one screening visit, 9 days of inpatient hospital admission, and a follow-up visit 2 weeks after discharge. - Participants will be screened with a physical exam and medical history. They will provide blood samples. - Participants will receive balanced-diet meals to take home for the 2 days before they enter the hospital. They will continue this diet while in the hospital. - During the inpatient stay, participants will be monitored with regular blood tests. They will have the following procedures: - Continued thyroid hormone replacement for all 9 days. - Drug to block thyroid enzyme for 7 days. - Metabolism test, with room temperature changes, on days 1, 2, 5, 8, and 9. - Measurements of body fat on days 2, 5, and 8. - Blood glucose tests on days 1 and 9. - Muscle contraction tests on days 1, 2, 4, 5, 8, and 9. - Heart imaging studies on days 2, 5, and 8. - Optional skeletal muscle and fat tissue biopsies on days 1 and 9. - There will be a follow-up visit 2 weeks after leaving the hospital. Participants will have a final physical exam and provide blood samples.

NCT ID: NCT01607242 Recruiting - Thyroidectomy Clinical Trials

Impact of Total Thyroidectomy on Voice and Swallowing

Start date: March 2012
Phase: N/A
Study type: Observational

Purpose of this study is to evaluate the outcome of total thyroidectomy on vocal and swallowing function.

NCT ID: NCT01189292 Completed - Thyroid Diseases Clinical Trials

Preoperative Single-dose Steroid Application for the Treatment of Nausea and Vomiting After Thyroid Surgery

tPONV
Start date: January 2011
Phase: Phase 3
Study type: Interventional

The study is to compare the postoperative recovery, as determined by postoperative nausea and vomiting (PONV) after preoperative application of single-dose dexamethasone versus saline in patients undergoing partial or total thyroidectomy.

NCT ID: NCT01171079 Completed - Thyroidectomy Clinical Trials

Use of an Oxidized Regenerated Cellulose After Thyroid Surgery: A Prospective, Randomized Study

ORC
Start date: n/a
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effects and safety of oxidized, regenerated cellulose as an absorbable adhesion barrier after thyroidectomy.

NCT ID: NCT01163045 Completed - Thyroidectomy Clinical Trials

Intraoperative Neuromonitoring of the Recurrent Laryngeal Nerve Versus Neurostimulation

Start date: January 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate if intraoperative neuromonitoring associated to neurostimulation of recurrent laryngeal nerve reduce the rate of recurrent laryngeal palsy respect to neurostimulation alone.

NCT ID: NCT01149239 Completed - Thyroidectomy Clinical Trials

The Effect of Preoperative Anxiety Level on the Induction Dose of Propofol and Minimum Alveolar Concentration (MAC) Hour of Sevoflurane During Thyroidectomy

Start date: June 2010
Phase: N/A
Study type: Observational

This study is to evaluate the level of anxiety, and to check the correlation of induction dose and the amount of sevoflurane to keep anesthetic depth in in female patients undergoing thyroidectomy.