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Pulmonary Complications clinical trials

View clinical trials related to Pulmonary Complications.

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NCT ID: NCT06255327 Completed - Clinical trials for Major Abdominal Surgery

Major Abdominal Surgery, Incidence of Pulmonary Complications, ICOUGH Care Program.

Start date: December 26, 2023
Phase: N/A
Study type: Interventional

This study aims to determine the efficacy of a suite of interventions for reducing postoperative pulmonary complications (PPCs) after major abdominal surgery (MAS), participants were subjected to the "I COUGH" care program designed to support their health condition and reduce complications. The study aimed to investigate a simple and inexpensive pulmonary care program that can be easily understood and remembered by patients, their families, and medical staff. To achieve this goal, we chose to implement the I COUGH care program and determine the effectiveness of a range of interventions to reduce PCs after MAS. Two hypotheses identified in the study: H0: The ICOUGH care program reduces the incidence of PPCs after MAS. H1: The ICOUGH care program after MAS does not affect the incidence of PPCs.

NCT ID: NCT02931409 Completed - Clinical trials for Inflammatory Response

Intraoperative PEEP Optimization: Effects on Postoperative Pulmonary Complications and Inflammatory Response

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

The purpose of this prospective randomized controlled trial is to determine the effects of intraoperative lung protective mechanical ventilation using an individual optimal PEEP value on postoperative pulmonary complications and inflammatory response. A total number of 40 patients undergoing open radical cystectomy and urinary diversion will be enrolled and randomized into two groups. Standard lung protective ventilation using a PEEP of 6 cmH2O will be performed in control group and an optimal PEEP value determined during a static pulmonary compliance (Cstat) directed PEEP titration procedure will be applyed in study group. Low tidal volumes (6mL/Kg IBW) and a fraction of inspired oxygen (FiO2) of 0.5 will be applyed in both groups. Procalcitonin kinetics will be monitored during and after surgery until the third postoperative day as well as postoperative pulmonary complications. Clinical condition and extrapulmonary complications will be evaluated by the Sequential Organ Failure Assessment (SOFA) Score and in-hospital stay, 28-days and in-hospital mortality will also be followed.

NCT ID: NCT02627742 Completed - Atelectasis Clinical Trials

Evaluation of The MetaNeb® System to Reduce Postoperative Pulmonary Complications

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

To determine if a therapy regimen including treatment with The MetaNeb® System had a positive impact on the rate of pulmonary complications related to atelectasis and/or secretion retention that occur in high risk post-operative patients. This is a non-randomized facility (or hospital) level pre-post intervention study.

NCT ID: NCT02373475 Completed - Clinical trials for Pulmonary Complications

Effect of Perioperative Lung Protective Strategies on the Occurrence of Postoperative Pulmonary Complications in Patients Undergoing Lumbar Spinal Surgery in the Prone Position

Start date: February 2015
Phase: Phase 4
Study type: Interventional

Postoperative pulmonary complications are main cause of overall perioperative morbidity and mortality in the patients following general anesthesia. A protective ventilation strategy refers to the use of low VT (in the range of 4-8 ml/kg of the predicted body weight) with positive end-expiratory pressure (PEEP), with or without recruitment maneuver. Protective ventilation has been considered the optimal practice in patients suffering from the acute respiratory distress syndrome (ARDS). However, few human studies have assessed how to ventilate healthy lungs in patients undergoing general anesthesia, especially in prone position. Prior studies reported that in the patients undergoing major abdominal surgery in supine position, intraoperative lung protective ventilator settings had the potential to protect against pulmonary complications. Therefore, the investigators planned this study to better specify the effect of intraoperative protective ventilation in surgical patients in the prone position.

NCT ID: NCT01285648 Completed - Lung Cancer Clinical Trials

Study of CPAP as Intervention After Lung Resection

CPAP
Start date: November 2007
Phase: N/A
Study type: Interventional

The aim of this study was to compare the oxygenation index (OI), dyspnea, and pain scale and evaluate the duration of thoracic drainage and pleural air leaks after lung resection in two groups of patients: chest physiotherapy (CP) patients and combined CP and Continuous Positive Airway Pressure (CPAP) patients.

NCT ID: NCT01219972 Completed - Clinical trials for Pulmonary Complications

Pulmonary Complications of Allografts

ALLOPULM
Start date: January 2006
Phase: N/A
Study type: Observational

This is a prognostic study of the late lung complications arising at the patient's having received an allograft of hematopoetic stem cells.

NCT ID: NCT01178567 Completed - Clinical trials for Pulmonary Complications

Comparison of Pulmonary Complications Related to Sleeve Gastrectomy and Gastric Banding

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

Comparison of Pulmonary Complications related to laparoscopic sleeve gastrectomy and laparoscopic adjustable gastric banding.

NCT ID: NCT01042132 Completed - Clinical trials for Systemic Inflammatory Response Syndrome

Intramedullary Femoral Reaming, Human Study

Start date: May 2003
Phase: N/A
Study type: Interventional

To what extent the cardiopulmonary and inflammatory response is affected by initial femoral intramedullary nailing in the already traumatized and inflammatory activated patient was analyzed in the present study with the attention to survey the additional burden of this operative treatment. The patients are monitored with a pulmonary catheter, and blood samples for coagulation, fibrinolysis, complement and cytokine response are withdrawn pre-, per- and postoperatively. The study is partly randomized 1)where delayed intramedullary nailing is compared with primary nailing of the femur, and 2) a new reaming technique (RIA) is compared with a standard reaming technique (TR).

NCT ID: NCT00933595 Completed - HIV Infections Clinical Trials

Longitudinal Studies of HIV-Associated Lung Infections and Complications (Lung HIV)

LHIV
Start date: September 2007
Phase: N/A
Study type: Interventional

The Lung HIV goal is to facilitate the data and specimen collection efforts of eight individual HIV and pulmonary studies that operate under the direction of the NHLBI. The Lung HIV study will build on existing studies to facilitate the start-up of new projects to further the understanding of the relationship between pulmonary disease and HIV infection. There is only one clinical trial being performed in this network at Ohio State University and it will be reported here.

NCT ID: NCT00897247 Completed - Clinical trials for Malignant Mesothelioma

Biomarkers to Detect Mesothelioma Early in Patients Exposed to Asbestos or Vermiculite

Start date: January 2007
Phase: N/A
Study type: Observational

RATIONALE: Studying samples of body fluid and blood from patients who have been exposed to asbestos or vermiculite in the laboratory may help doctors learn more about changes that may occur in DNA and identify biomarkers related to cancer. PURPOSE: This laboratory study is looking for biomarkers to detect mesothelioma early in patients exposed to asbestos or vermiculite.