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Thyroidectomy clinical trials

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NCT ID: NCT01146431 Recruiting - Thyroidectomy Clinical Trials

Memory During Inhalation Anesthesia Performed With or Without Bispectral Index (BIS) in Patients Undergoing Thyroidectomy

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

The purpose of this study is 1) to investigate whether the use of BIS as a guide to the administration of inhaled anesthetic (sevoflurane or desflurane) compared with the use of hemodynamic parameters (blood pressure and heart rate) would affect the occurrence of implicit memory and /or dreams recall and 2) to check whether the occurrence of implicit memory and/or dreams recall is related with MAC (Minimal Alveolar Concentration) of inhalational anesthetics and/or preoperative anxiety levels.

NCT ID: NCT01126060 Completed - Thyroidectomy Clinical Trials

Efficacy of Fibrin Sealant to Reduce the Amount of Post-thyroidectomy Drain

Start date: February 2010
Phase: Phase 3
Study type: Interventional

Fibrin sealant has been studied to reduce post-thyroidectomy drain and hospital stay as well. However, no strong evidence from well-designed clinical trials is available. Harmonic scalpel is a ultrasonic vibrating scissors which makes it easy to cut and coagulate the tissues, thus reducing op time and postoperative drain, which is important to minimize hospital stay. The investigators hypothesized that fibrin sealant combined with harmonic scalpel-assisted procedure could guarantee no-drain postoperative care in total thyroidectomy with anterior compartment neck dissection.

NCT ID: NCT01082458 Completed - Thyroidectomy Clinical Trials

Comparison of Lidocaine and Remifentanil for the Effect on Responses to the Endotracheal Tube During Emergence From General Anesthesia

Start date: February 2010
Phase: N/A
Study type: Interventional

Target concentration infusion(TCI) of remifentanil (2.0ng/ml) suppresses the cough induced by endotracheal tube more effectively than intravenous administration of lidocaine (1.5mg/kg).

NCT ID: NCT01075269 Active, not recruiting - Surgery Clinical Trials

Postoperative Distress and Cosmetic Outcomes After Open Versus Robotic Thyroidectomy

Robot1
Start date: April 2009
Phase: N/A
Study type: Observational

Robotic assistance during thyroid surgery has been utilized clinically in Korea since late 2007. Robotic thyroidectomy has also been validated for surgical management of the thyroid gland. Compared with endoscopic thyroidectomy, the use of a robot in an endoscopic approach via the axilla provides a broader view of the thyroid bed, albeit from a lateral, as opposed to the conventional anterior, perspective. The wrist action of a surgical robot also provides a greater degree of movement than afforded by the use of simple endoscopic instruments, and tremor is eliminated. Although several reports on operative outcomes of the robotic technique have appeared, no prospective trials comparing the clinical results of robotic with conventional open thyroidectomy have been described. We therefore designed a prospective trial comparing outcomes, including postoperative distress and patient satisfaction, between patients undergoing robotic and conventional open thyroidectomy.

NCT ID: NCT01039714 Recruiting - Clinical trials for Vitamin D Deficiency

Vitamin D Levels and Postoperative Hypocalcemia After Total Thyroidectomy

Start date: December 2009
Phase: N/A
Study type: Observational

Hypocalcemia is one of the most frequent complications of total thyroidectomy, a procedure used for benign as well as malignant conditions of the thyroid gland. Postoperative hypocalcemia is usually caused by hypoparathyroidism. Vitamin D is implicated in calcium metabolism as it increases intestinal calcium transport and regulates parathormone production. Aim of the present study is to evaluate preoperative vitamin D levels as a prognostic factor for postoperative hypocalcemia and hypoparathyroidism.

NCT ID: NCT00892164 Completed - Thyroidectomy Clinical Trials

Thyroid Surgery With the New Harmonic Scalpel or the Electrothermal Bipolar Vessel Sealer

Start date: August 2008
Phase: N/A
Study type: Interventional

The objective of this study is to compare the results of total thyroidectomy using the new harmonic scalpel device to that with the electrothermal bipolar vessel sealer.

NCT ID: NCT00888303 Recruiting - Postoperative Pain Clinical Trials

Single Dose Steroid Before Thyroidectomy for Benign Disease to Improve Postoperative Nausea, Pain, and Vocal Function

Start date: January 2009
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the efficacy of 8 mg of dexamethasone administered prior surgery, to reduce pain, postoperative nausea and vomiting and to improve vocal function after thyroidectomy for benign disease.

NCT ID: NCT00784407 Completed - Thyroidectomy Clinical Trials

Thyroid Surgery With the New Harmonic Scalpel: a Prospective Randomized Study

Start date: February 2008
Phase: N/A
Study type: Interventional

The objective of this study is to compare the results of total thyroidectomy using the new harmonic scalpel device (FOCUS) to that with the previously available harmonic scalpel device (HARMONIC ACE).

NCT ID: NCT00520338 Completed - Postoperative Pain Clinical Trials

Celecoxib for Reducing Morphine Requirement After Thyroid Surgery: A Randomized Controlled Trial

Start date: August 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether celecoxib is effective in the treatment postoperative pain after thyroidectomy. The research hypothesis: There is a difference in postoperative morphine consumption in the first 24 hours after thyroidectomy between patients who received celecoxib or placebo.

NCT ID: NCT00472446 Completed - Thyroidectomy Clinical Trials

Cervical Block in Thyroid Surgery

Start date: January 2006
Phase: Phase 2/Phase 3
Study type: Interventional

The study investigates the impact on post-operative pain of the superficial cervical block with bupivacaine combined with subcutaneous infiltration of the incisional area in thyroid surgery under general anesthesia. In addition, cost savings using the cervical block are evaluated (due to reduced length of hospital stay). The study is prospective, randomized, double blind, and placebo-controlled. The study is performed at the Department of Surgery, Cantonal Hospital of St. Gallen.