Risk Factors for Postoperative Cough in Patients Undergoing Thoracoscopic Lung Resection

ConditionLung Cancer
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-70
SponsorHematology department of the 920th hospital

About this trial

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 criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

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.)

Trial population

The participants in this study are from the 920th Hospital. Patients aged 18 years or older and less than or equal to 70 years of age who underwent surgery with video-assisted thoracoscopic pneumonectomy.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • without

    Other intervention

    without

Treatment groups

1,000 Participants
are divided into 2 treatment groups
Group A: cough1 intervention
Group B: Uncough1 intervention

Trial outcomes

Primary outcomes

1

The score value of Mandarin Chinese version of the Leicester Cough Questionnaire

Mandarin Chinese version of the Leicester Cough Questionnaire is a globally recognized questionnaire for assessing the severity of cough

Time frame
On the 3rd,1 month and Half a year postoperatively
2

The score value of visual analogue scale

The score value of visual analogue scaleis a globally recognized questionnaire for assessing the severity of cough

Time frame
On the 3rd, 7th, 11th, 15th, 1 month, and half a year after surgery, respectively

Secondary outcomes

1

The score value of Hull airway reflux questionnaire

The score value of visual analogue scaleis a globally recognized questionnaire for assessing the severity of cough

Time frame
On the 3rd,1 month and Half a year postoperatively

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.