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Clinical Trials in China / NCT06476249
Recruiting Observational

Risk Factors for Postoperative Cough in Patients Undergoing Thoracoscopic Lung Resection

NCT06476249 · tracked via the Priya Life Science China tracker
Sponsor
Hematology department of the 920th hospital
Phase
Observational
Started
2024-03-01
Last updated
2024-06-28

Condition(s) studied

Lung Cancer

Investigational drug(s) / intervention(s)

without

without: without

Study summary

Lung cancer, as the main cause of cancer-related deaths in both males and females, is a great risk to human health. Pulmonary resection is the most applicable to early-stage lung cancer diagnoses and considered the best curative options. Coughing is a prominent symptom among postoperative complications, with approximately 18%-50% of patients experiencing persistent coughing after surgery. This study is a prospective observational study and is expected to be carried out in a large tertiary hospital. This cohort is expected to include 1000 participants for three years.

Patients with pulmonary nodules on chest CT will be divided into two groups based on the presence or absence of cough symptoms on admission. The investigators decided whether to include patients in this cohort study strictly based on the inclusion and exclusion criteria. The severity of cough, the trajectory of cough change, and the physiological and social burden caused by cough will be reflected by the results of LCQ-MC, CSS, HARQ, and VAS. LCQ-MC, CSS, HARQ, and VAS are just a few of the questionnaires that are widely used to investigate the cough and severity of the respondent. The included variables included age, gender, Height, Weight, education level, smoking history, alcohol history, preoperative lung function, nodule size, preoperative and postoperative blood routine (such as white blood cell count, neutrophil count, etc.), blood biochemistry (such as C-reactive protein, PCT, etc.), liver and kidney function test results, surgical method, surgical site, operation duration, anesthesia method, anesthesia duration, lymph node dissection, pathological results, chest tube caliber, number of days of catheterization, use of cough drugs, use of non-steroidal anti-inflammatory drugs, Number of days in hospital and number of outpatient visits due to cough.

Eligibility

Sex
ALL
Min age
18 Years
Max age
70 Years
Healthy volunteers
No
Inclusion Criteria: ● Patients aged 18 years or older and less than or equal to 70 years of age who underwent surgery with video-assisted thoracoscopic pneumonectomy. Exclusion Criteria: * Pre-existing cough before surgery (e.g. asthma, taking ACEI Drugs, etc.) * Distant metastasis of tumor * Combined pregnancy or breastfeeding * Combined with other systemic major diseases (such as malignant swelling, chronic liver insufficiency, chronic renal insufficiency, etc.) * Suffering from mental illness * Refusal of follow-up or incomplete clinical information * Poor compliance and other groups considered by the investigator not suitable for inclusion

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
the 920th Hospital of the Joint Logistics Support Force Kunming Yunnan Recruiting

More Hematology department of the 920th hospital trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06476249 on ClinicalTrials.gov ↗ ← All trials in China