A Study of Smoking Cessation Patterns in Participants Undergoing Lung Surgery (CHAMPION)

Johnson & Johnson (J&J)

Status: Completed

Conditions: Lung Neoplasms; Pulmonary Disease, Chronic Obstructive

Treatments: Other: No intervention

Study type: Observational

Funder types: Industry

Identifiers

NCT04313361

NOPRODLUC4001 (Other Identifier)

CR108767

Details and patient eligibility

About

The purpose of this study is to assess the current smoking status and smoking cessation attempts among smokers or recent smoking quitters during the perioperative period, to describe postoperative pulmonary complications (PPCs) and other postoperative complications (PCs) following a lung surgery, and to describe the smoking cessation methods and services patients received from their health care professionals (HCPs) and participant's satisfaction among participants with lung cancer, chronic obstructive pulmonary disorder (COPD), a pulmonary lesion (example, nodule, or ground glass opacity) or other pulmonary conditions who are admitted to the thoracic surgical unit of the participating hospitals in China.

Enrollment: 290 patients

Sex: All

Ages: 40 to 80 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Participants who have been scheduled for an elective lung surgery by the treating physician's judgement, due to the following conditions: known lung cancer, COPD, a pulmonary lesion (example. nodule, ground glass opacity) or other pulmonary conditions
• Smokers who are or were smoking on average no fewer than 5 cigarettes per day for equal or more than 3 years within 3 months prior to the scheduled surgery, or recent smoking quitters with a history of smoking on average no fewer than 5 cigarettes per day for equal or more than 3 years, who quit smoking between 3 months and 5 years prior to the scheduled surgery
• Being willing to participate the study and sign the participant informed consent form (ICF)

Exclusion criteria

• Participants who have emergency lung surgery due to accident or injury
• Participants are not likely to be able to complete the 6-month follow-up after the lung surgery

Trial design

290 participants in 1 patient group

Smokers or Recent Smoking Quitters who Have lung Surgery

Description:

The enrolled eligible participants, that is smokers or recent smoking quitters, will be assessed for the current smoking status and smoking cessation attempts during the perioperative period, to describe postoperative complications (PCs) including postoperative pulmonary complications (PPCs) following a lung surgery, and to describe the smoking cessation methods and services participants received from their health care professionals (HCPs) and participant's satisfaction among participants with lung cancer, chronic obstructive pulmonary disorder (COPD), a pulmonary lesion (example nodule, ground glass opacity) or other pulmonary conditions who are admitted to the thoracic surgical unit of the participating hospitals in China.

Treatment:

Other: No intervention