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Funnel Chest clinical trials

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NCT ID: NCT03346876 Recruiting - Surgery Clinical Trials

Autonomic Dysfunction in Patients With Pectus Excavatum.

ADPE
Start date: August 1, 2017
Phase: N/A
Study type: Observational [Patient Registry]

Investigators conducted a pilot study to to evaluate the autonomic function in participants with pectus excavatum before and after Nuss surgery.

NCT ID: NCT03087734 Completed - Funnel Chest Clinical Trials

Evaluation of a New Model of Metallic Bar and Stabilizer for Use in MIRPE

Start date: October 3, 2017
Phase: N/A
Study type: Interventional

Pectus excavatum (PE) is the most common deformity of the chest wall, occurring in approximately 1/1000 people. Currently, surgical treatment by minimally invasive technique is consolidating as preferred technique for the treatment of this condition. In this technique a metal bar is inserted in retrosternal position, pushing the sternum without the necessity of resecting the condral cartilages. Despite the advantages obtained with this technique, it is not without complications and the displacement of the bar is one of the most important. In order to minimize this problem we developed a new model of stabilizers, as well as all necessary instruments for performing minimally invasive surgery. The aim of this study is to compare two surgical groups, one making use of the new oblique stabilizer compared to the conventional perpendicular stabilizer to determine which one has less displacement. Furthermore, this study also aims to assess the full range of instruments developed by a national company, to carry out this type of surgery, which has cost compatible with our economic reality, and that can be accessible to our Public Health patients.

NCT ID: NCT03086499 Completed - Funnel Chest Clinical Trials

Clustering Among the Clinical Profiles of Patients With Pectus Excavatum

PECTUS-cluster
Start date: March 25, 2017
Phase: N/A
Study type: Observational

The primary objective of this study is to describe the relative distances between patient clinical profiles (i.e. patient clustering) in multivariate space.

NCT ID: NCT03073616 Completed - Pectus Excavatum Clinical Trials

Lung Ultrasound for the Postoperative Diagnosis of Pneumothorax in Children

ECO_NUSS
Start date: April 1, 2017
Phase:
Study type: Observational

This study will be conducted to determine the advantages and limitations of sonography compared with chest radiography, in the detection of post procedure iatrogenic pneumothorax in patients underwent to Pectus Excavatum (PE) with Nuss repair.

NCT ID: NCT02958683 Completed - Surgery Clinical Trials

Chest Wall Motion Analysis in Disease

CWM
Start date: July 2011
Phase:
Study type: Observational

Breathing movements, called chest wall motion, are very complex. The investigators are studying how movement of the abdomen, ribs and diaphragm contribute to breathing and how this differs with different diseases in the chest. Breathing movements may help with diagnosis, assessment of severity or assessing the impact of treatments for chest conditions. The investigators are following people who have a chest disease, measuring their chest wall motion and comparing it to their diagnosis and and how their treatment works. Chest wall motion can be measured in different ways at rest and whilst exercising. Small stickers on the chest can be used to reflect infra red light or visible squares of light can be shone onto the chest without using stickers.

NCT ID: NCT02721017 Completed - Pectus Excavatum Clinical Trials

Cryoanalgesia vs. Epidural in the Nuss Procedure

Start date: May 2016
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether cryoanalgesia provides better pain control for minimally invasive pectus excavatum repair (the Nuss procedure) than thoracic epidural.

NCT ID: NCT02552186 Completed - Pectus Excavatum Clinical Trials

Non-invasive Clinical Pectus Index as a Measurement of Severity in Pectus

Start date: September 2015
Phase: N/A
Study type: Interventional

Pectus excavatum (PE), the most common congenital chest wall deformity, requires surgical repair when the degree of deformity is severe. Currently, the Pectus Index (PI) is used to classify PE severity. Calculation of the PI requires cross-sectional imaging of the chest, usually with computed tomography (CT) or Magnetic Resonance Imaging (MRI), to obtain the necessary measurements. However, CT delivers a high dose of ionizing radiation, which carries cumulative long-term risks of malignancy and MRI can be costly. The purpose of this study is to develop a method whereby accurate chest wall measurements can be obtained to quantify PE severity without the need for cross-sectional imaging.

NCT ID: NCT02528656 Recruiting - Pectus Excavatum Clinical Trials

Physiological Assessments During Non Operative Treatment on the Chest Wall Deformities

PECTUS
Start date: January 12, 2015
Phase: N/A
Study type: Interventional

The physiological assessment in non-operative treatment on chest wall deformities, are still unclear today. These functional benefits outweigh the aesthetic benefits associated with anatomical improvement. The functional benefits, ventilation, hemodynamic and neurologic, have never been evaluated. Assessment of Effects on parasympathetic activity of the autonomic nervous system, global health criterion measured by noninvasive methods. Anatomic evaluation, between the initial and final assessment by objective measures 1) of the chest wall by MRI, and 2) of the heart by echocardiography. Noninvasive physiological assessment at rest and during exercise in respiratory function exploration flows and volumes, cardiac function by flow measurement, and overall metabolic function test effort (VO2max). Subjective assessment of functional gain between the initial and final balance sheet, based on EVA scales, valued by patients, parents and doctors.

NCT ID: NCT02441452 Completed - Funnel Chest Clinical Trials

Functional Capacity of Exercise and Lung Function in Patients Submitted Early Rehabilitation

Start date: January 2013
Phase: N/A
Study type: Interventional

The aim of this study was to compare the functional capacity of exercise by six-minute walk test and lung function by spirometry, before and after Nuss procedure in subjects who have undergone the early rehabiliation program with those who were under conventional care. Researchers want to find out if early rehabilitation is a strategy to enhance recovery after Nuss procedure.

NCT ID: NCT02376634 Withdrawn - Scoliosis Clinical Trials

Hypnotherapy in Major Surgical Procedures

Start date: June 2016
Phase: N/A
Study type: Interventional

The purpose of this randomized controlled study is to test the feasibility of clinical hypnotherapy as a perioperative intervention for the reduction of pre-operative anxiety, post-operative pain, and other-related symptoms (nausea, vomiting, spasms, length of stay, self mastery) in children undergoing scoliosis repair or Nuss procedure.