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Surgery, Thoracic clinical trials

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NCT ID: NCT03488459 Completed - Pain, Postoperative Clinical Trials

Influence of Preoperative Support on Anxiety, Pain and Satisfaction With Postoperative Analgesia

Start date: March 1, 2012
Phase: N/A
Study type: Interventional

The aim of this study was to analyze a relationship between information support provided by an interdisciplinary team and the levels of anxiety, pain and satisfaction with postoperative analgesia in children and adolescents subjected to thoracic surgeries.

NCT ID: NCT03444636 Completed - Pain, Postoperative Clinical Trials

Multimodal Analgesia in Children and Adolescents After the Ravitch Procedure and Thoracotomy

Start date: March 2, 2015
Phase: Phase 4
Study type: Interventional

The study was performed in patients aged 6-18 years after the Ravitch procedure and thoracotomy. The primary aim of the study was to evaluate the efficacy and safety of pain control provided by the multimodal approach that involves the continuous infusion ropivacaine with fentanyl vs. bupivacaine with fentanyl through thoracic epidural catheter. Secondary aims were to identify the determinants of acute post-operative pain at rest, during deep breathing and coughing.

NCT ID: NCT03393702 Completed - Pain, Postoperative Clinical Trials

Pain Control in Children and Adolescent After Thoracic Surgery: The Effect of Gabapentin

Start date: May 9, 2017
Phase: Phase 4
Study type: Interventional

The study is performed in patients aged 5-18 years after thoracic surgery. The primary aim of this trial is to determine whether the use of gabapentin as a component of multimodal analgesic regiments reduces pain scores following thoracic surgery in pediatric patients. The secondary objective of the trial are to evaluate whether the use of gabapentin reduces postoperative anxiety scores and consumption of ropivacaine with fentanyl, decreases side-effects, and improves patient satisfaction.

NCT ID: NCT03347578 Completed - Clinical trials for Complication, Postoperative

Diaphragmatic Echography After Thoracic Surgery

OLVDD
Start date: February 2016
Phase:
Study type: Observational

The investigator evaluated diaphragmatic function in patients undergoing thoracic surgery. Diaphragmatic displacement was evaluated before surgery, 2 and 24 hours after surgery. Also, preoperative spirometry and postoperative spirometry were collected (24 hours after surgery).