A Study to Explore the Early Subjective Evaluation and Objective Recovery in Lung Cancer Patients Undergoing Sublobar Resection Versus Lobectomy

Guangzhou Medical University

Status: Enrolling

Conditions: Sublobar Resection; Lung Cancer (Diagnosis); Lobectomy

Study type: Observational

Funder types: Other

Identifiers

NCT07288710

GMU-LC-202511

Details and patient eligibility

About

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.

Enrollment: 300 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. adult patients (age ≥ 18 years)
2. American Society of Anesthesiologists (ASA) grade of III or below
3. scheduled for VATS from March to December 2023

Exclusion criteria

1. age <18 years
2. inability or poor compliance to use wearable devices
3. lack of smartphone
4. incomplete digital device data during hospitalization
5. patients with lymph node or distant metastasis

Trial design

300 participants in 2 patient groups

Sublobar Resection Group

Description:

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

Description:

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.