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Lung Cancer clinical trials

View clinical trials related to Lung Cancer.

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NCT ID: NCT04739696 Active, not recruiting - Breast Cancer Clinical Trials

Developing a Virtual Stress Management Intervention for Spousal/Partnered Caregivers of Solid Tumor Cancer Patients.

eCare
Start date: February 5, 2021
Phase: N/A
Study type: Interventional

This randomized control trial will investigate the ability of an effective stress management psychoeducation program for employed caregivers to mitigate psychological distress and pathophysiology in spousal or partnered caregivers of patients' diagnosis with a solid tumor cancer of any stage. It is expected that improving caregiver status will have reduced depressive symptoms.

NCT ID: NCT04736173 Active, not recruiting - Lung Cancer Clinical Trials

Study Comparing the Combination Domvanalimab and Zimberelimab With Pembrolizumab in Untreated Locally Advanced or Metastatic PD-L1-High Non-Small Cell Lung Cancer

ARC-10
Start date: February 8, 2021
Phase: Phase 3
Study type: Interventional

This is a phase 3 study to evaluate zimberelimab (AB122) combined with domvanalimab (AB154) compared to pembrolizumab in front-line, PD-L1-high, locally advanced or metastatic NSCLC.

NCT ID: NCT04735614 Completed - Lung Cancer Clinical Trials

Physical Stabilization in Post-VATS

Start date: January 27, 2021
Phase: N/A
Study type: Interventional

Background: Post-video-assisted thoracic surgery (VATS) pain remains an open issue, though most patients experience less acute pain after VATS than thoracotomy. So far, there was no gold standard regarding pain control post-VATS. Objective: To conduct a randomized controlled trial assessing the effect of physical thoracic stabilization on post-VATS pain control. Method: The investigators aimed to recruit 40 patients with operable lung cancer in the outpatient clinic from January to December 2021. The patients will be randomized into the intervention or control group. The intervention group will receive physical thoracic stabilization with POSTHORAX ThoraxBelt after the surgery, whereas the control group will have standard care. The follow-up period will last for 6 months.

NCT ID: NCT04735341 Completed - Lung Cancer Clinical Trials

Prospective Post-market Data Collection for Ion Endoluminal System to Understand CT to Body Divergence

Start date: December 9, 2020
Phase:
Study type: Observational

The goal of this study is to collect post-market data for the Ion Endoluminal System to understand CT to body divergence.

NCT ID: NCT04734145 Active, not recruiting - Lung Cancer Clinical Trials

Using e-Nose Technology to Identify Early Lung Cancer

Start date: January 25, 2021
Phase:
Study type: Observational

The purpose of this study is to test the ability of a new technology called breathprinting, or electronic nose (e-nose), to detect early-stage lung cancer. Additionally, researchers also want to see if the e-nose technology is more effective at diagnosing lung cancer if the tumor size is larger.

NCT ID: NCT04733430 Recruiting - Lung Cancer Clinical Trials

LALUCA Research Platform A Prospective Analysis of Lung Cancer Diagnosis and Management in Clinical Practice

LALUCA
Start date: April 17, 2020
Phase:
Study type: Observational [Patient Registry]

This is a prospective analysis of the diagnosis and treatment of lung cancer in a real-world setting. The aim of the project is to establish a clinical platform to collect representative data on molecular testing, sequence of systemic tumor therapy and other therapies, and disease progression of patients with lung cancer. A special focus will be on molecular biomarker testing and reflex NGS testing. Another aim of the registry is the collection of quality indicators in lung cancer care. The results of the register will be used to describe the current state of care and to develop it further for the future.

NCT ID: NCT04731909 Recruiting - Lung Cancer Clinical Trials

Toripalimab Combined With Anlotinib, Etoposide and Platinum in the Treatment of Extensive-stage Small Cell Lung Cancer

Start date: October 1, 2018
Phase: N/A
Study type: Interventional

To evaluates the effectiveness and safety of Toripalimab combined with Anlotinib and chemotherapy for the first-line treatment of ES-SCLC, and maintenance therapy are Toripalimab combined with Anlotinib.

NCT ID: NCT04730453 Recruiting - Lung Cancer Clinical Trials

ENB-guided Ablation Therapy Combined With VATS in the Treatment of MPLC

Start date: July 24, 2020
Phase:
Study type: Observational

The study is designed as a prospective trial whose purpose is to evaluate the effectiveness and safety of ENB-guided ablation therapy combined with VATS in the treatment of multiple primary lung cancers (MPLC).

NCT ID: NCT04722432 Completed - Lung Cancer Clinical Trials

Evaluation of Deployment Capability and Accuracy of an Outside the Scope (OTS), Detachable Catheter System for Ablation of Peripheral Lung Lesions: An Ex-Vivo Human Lung Model Study

Start date: October 16, 2020
Phase: N/A
Study type: Interventional

A novel OTS detachable probe system carried outside and along the flexible bronchoscope has been developed. Using this novel system, the operator can deploy the probe in the target bronchus and lesion and completely detach the scope from the probe.

NCT ID: NCT04722393 Completed - Lung Cancer Clinical Trials

Lung Resection and Pulmonary Rehabilitation

Start date: October 1, 2017
Phase: N/A
Study type: Interventional

Lung cancer is the most common cancer in the world and surgical resection remains the gold standard curative treatment in early stage non-small cell lung cancer. However, surgery itself is the direct cause of pulmonary function impairment, which dramatically reduces patients tolerance to exercise and their quality of life. Pulmonary rehabilitation (PR) complements surgical treatment and improves patients' exercise and functional capacity, decreases dyspnea, improves health status. Our aim is to examine the effectiveness of PR applied after lung resection in patients with lung cancer, 2- To determine whether the respiratory exercise training given to patients who could not participate in the PR program is effective.