NCT07232394Completed
Early Feeding and Mobilization in Thoracic Surgery
The Impact of Early Feeding and Mobilization on Rehabilitation in Thoracic Surgery: A Prospective Randomized Controlled Trial
Source: ClinicalTrials.gov · Last updated 27 Oct 2026
Brief summary (registry, in English)
This study evaluates the safety and effectiveness of an innovative care assessment tool for early feeding and mobilization following thoracic surgery, based on the Enhanced Recovery After Surgery (ERAS) protocol. The aim is to improve postoperative recovery by helping healthcare providers implement a structured, evidence-based plan for early feeding and activity. The study will compare the new care model (ERAS-based) with traditional postoperative care. The investigators will focus on outcomes like recovery quality, complications, hospital stay, and medication use. This research aims to provide solid evidence for integrating early feeding and mobilization into routine thoracic surgery recovery, potentially improving patient comfort, reducing recovery time, and lowering complications.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 300 (actual)
- First submitted
- 13 Nov 2025
- Start date
- 1 Jan 2026
- Primary completion date
- 1 Jun 2026
- Lead sponsor
- Jianxing He
- Diseases
- Lung cancer
- NCT number
- NCT07232394
What you commit to
- Study type: Interventional
- Participants enrolled: 300
- From 1 Jan 2026 to the primary completion date, 1 Jun 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Requirement to convert to open surgery during the procedure;
Other illness
- Patients with cognitive impairment, mental illness, or other conditions that may affect the study;
- Lung cancer with metastasis to other organs;
- Failure to sign the informed consent form.
Who the study is looking for
- Aged 18 to 75 years, with no gender restrictions;
- Planned for elective thoracoscopic surgery, in good physical condition, able to undergo surgery and anesthesia (ASA classification no more than class III), and confirmed suitable for surgery after joint assessment by the medical and nursing team;
- No severe cognitive impairment or mental illness, able to cooperate with nursing staff and follow intervention measures;
- Normal function of major organs;
- The patient has provided informed consent to participate in the study and signed the informed consent form.
Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| The First Affiliated Hospital of Guangzhou Medical University Coordinator of this site? Confirm its status | Guangzhou | China | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.