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Thoracotomy clinical trials

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NCT ID: NCT04443556 Completed - Postoperative Pain Clinical Trials

Effect of Continue RISS Block in Thoracotomy

Start date: August 31, 2020
Phase: N/A
Study type: Interventional

Thoracotomy is one of the most painful surgery. Acute postoperative pain increases postoperative morbidity and prolongs hospital stay and also may lead to developing a chronic pain syndrome. This study aimed to assess the efficacy of continuous rhomboid intercostal and subserratus plane (RISS) block by inserting a catheter under direct vision for controlling acute thoracotomy pain.

NCT ID: NCT04242160 Completed - Trauma Clinical Trials

Comparison of Two Resuscitative Thoracotomy Techniques

Start date: November 19, 2018
Phase: N/A
Study type: Interventional

Resuscitative thoracotomy (RT) is a life saving procedure for patients who have suffered cardiac arrest or are at significant risk of cardiac arrest following significant trauma. The procedure is ideally performed by a surgeon, but in some circumstance must be performed by non-surgical specialists such as Emergency Medicine physicians. The purpose of this study was to evaluate the optimal RT technique taught to non-surgical specialists in an educational human cadaver lab. The objective was to compare time to successful completion of two different RT techniques; (1) Left Anterolateral Thoracotomy (LAT) and (2) Modified Clamshell Thoracotomy (MCT). The investigators hypothesized that the non-surgical specialist time to successful completion for the MCT would be shorter than for the LAT.

NCT ID: NCT03839160 Completed - Anesthesia Clinical Trials

The Efficacy of Serratus Anterior Plane Block (ESAPB) for Thoracotomy: a Prospective Study

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

Thoracotomy is considered the most painful surgical procedure. Ultrasound-guided serratus anterior plane block (SAPB) is a relatively new truncal block method treating thoracotomy pain. In this study, investigators aim to ascertain the efficacy of SAPB in thoracotomy.

NCT ID: NCT03281213 Completed - Postoperative Pain Clinical Trials

Acute Postthoracotomy Pain - Impact of Gender

Start date: July 1, 2010
Phase: N/A
Study type: Observational

Adequate analgesia in thoracic surgery is essential to prevent severe postoperative complications, especially respiratory problems. Current knowledge about gender-related differences in pain states generally more frequent and intense pain and more demand for analgesics in women. Results about postsurgical pain in particular are very inconclusive. The investigators tried to find out if gender has an influence on postthoracotomy pain and analgesics requirement.

NCT ID: NCT02073760 Completed - Sepsis Clinical Trials

Optimizing Prevention of Healthcare-Acquired Infections After Cardiac Surgery (HAI)_2

Start date: June 2014
Phase:
Study type: Observational

The investigators will conduct qualitative interviews of hospital personnel regarding HAI prevention practices, and use coded data from these interviews to assist in developing standardized practices.

NCT ID: NCT01698203 Completed - Pain Clinical Trials

Continuous Wound Catheter Analgesia Associated With Intravenous Morphine PCA After Thoracotomy

Start date: October 14, 2012
Phase: Phase 4
Study type: Interventional

Objective: Epidural analgesia is the gold standard for post-thoracotomy pain relief but is contraindicated in certain patients. An alternative is continuous wound catheter analgesia. We will investigate whether ropivacaine, administered through a wound catheter placed by the surgeon, will reduce postoperative pain. Methods: In a randomized double-blind study, adult patients with a wound catheter placed by the thoracic surgeon after thoracotomy will be randomly assigned to receive through this catheter, either a 0.1 mL/kg bolus of 0.75% ropivacaine, followed by a continuous infusion of 0.2% ropivacaine at 10 mL/h for 48 h, or saline at the same scheme of administration. Patients will also benefit from patient-controlled analgesia with intravenous morphine (bolus 1 mg, lockout time 7 min), paracetamol, and nefopam. The primary endpoint will be total morphine consumption. Secondary endpoints will be pain intensity on a visual analog scale at rest and on coughing and side effects during the first 48 postoperative hours. Surgeons, anesthesiologists, and all the nurses and caring staff involved in this study will be blinded. Solutions of saline and ropivacaine will be prepared identically by the central pharmacy, without any possible identification of the product.

NCT ID: NCT01274871 Completed - Chronic Pain Clinical Trials

Sensory Changes From Chest Drains

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

Does chest drains contribute to the post thoracotomy pain syndrome

NCT ID: NCT01076894 Completed - Thoracotomy Clinical Trials

Thoracotomy: Intercostal Nerve Block Versus Epidural Anesthesia

Start date: February 2007
Phase: N/A
Study type: Interventional

Postoperative pain and consecutive reduction of pulmonary function after thoracic surgery still is a major clinical problem and challenge in anesthesia. Thoracic epidural anesthesia is commonly considered to be the "gold standard" for postoperative pain control and restoration of pulmonary function after thoracic surgery. Thus, the aim of the present study is to investigate whether an intercostal nerve block with ropivacaine plus intravenous PCA with morphine is as effective as thoracic epidural anesthesia with respect to postoperative pain control and pulmonary

NCT ID: NCT00976313 Completed - Thoracotomy Clinical Trials

Does Thoracic Epidural Analgesia Influence Urinary Micturition by Patients Undergoing Thoracic Surgery?

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

Under the influence of epidural analgesia, patients may not feel the urge to urinate, which can result in urinary retention and bladder overdistension. The use of a transurethral catheter is associated with significant morbidity such as patient discomfort, urinary tract infections, urethral trauma and stricture. Urodynamic changes under thoracic epidural anaesthesia are still unknown. The aim of this study is to compare lower urinary tract function before and during thoracic epidural analgesia within segments T2 to T10 for postoperative pain treatment in patients undergoing thoracotomy or sternotomy.

NCT ID: NCT00910949 Completed - Chronic Pain Clinical Trials

Sensory Perception After Thoracotomy

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

The study will investigate characteristics of chronic pain after thoracotomy