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The trial was designed as a single-center, non-interventional, prospective observational study to explore the role of a multimodal digital device in analyzing subjective and objective recovery in lung cancer patients undergoing sublobar resection versus lobectomy.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Sublobar Resection Group | Patients in this group underwent sublobar resection (including segmentectomy or wedge resection). The decision for patients to receive this surgical procedure was similarly based on their routine clinical assessment, disease characteristics, physician's recommendation, and informed consent. It was not a result of randomization or active intervention by the investigators. This study will prospectively observe the post-operative recovery and prognosis of these patients, comparing them to the lobectomy group. | ||
| Lobectomy Group | Patients in this group underwent standard lobectomy. The decision for patients to receive this surgical procedure was based on their routine clinical assessment, diagnosis, disease staging, physician's recommendation, and informed consent. It was not a result of randomization or active intervention by the investigators. This study will prospectively observe the post-operative recovery and prognosis of these patients. |
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| Measure | Description | Time Frame |
|---|---|---|
| Electronic patient-reported outcomes | The electronic patient-reported outcomes questionnaire includes pain, cough, shortness of breath, restless sleep, fatigue, drowsiness, walking difficulties, activity limitation, and distress(0 = no symptom, 10 = most severe). | From 1 day prior to surgery through hospital discharge (assessed up to 15 days). |
| Measure | Description | Time Frame |
|---|---|---|
| Length of Hospital Stay | Total number of days spent in the hospital from admission to discharge. | From the day of surgery until the day of discharge, assessed up to 15 days. |
| Surgical Time | Duration of the surgery measured in hours. |
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Inclusion Criteria:
Exclusion Criteria:
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All patients with histopathologically confirmed lung cancer were consecutively recruited
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Department of Thoracic Surgery and Oncology, The First Affiliated Hospital of Guangzhou Medical University | Guangzhou | Guangdong | China |
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| During the surgical procedure (from anesthesia induction until skin closure). |
| Number of Lymph Nodes Dissected | The total count of lymph nodes harvested during the surgical procedure. | During the surgical procedure (from anesthesia induction until skin closure). |
| ID | Term |
|---|---|
| D008175 | Lung Neoplasms |
| D004194 | Disease |
| ID | Term |
|---|---|
| D012142 | Respiratory Tract Neoplasms |
| D013899 | Thoracic Neoplasms |
| D009371 | Neoplasms by Site |
| D009369 | Neoplasms |
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
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