Evaluating patient outcomes in enhanced recovery after surgery nursing
Effect of ERAS Nursing on Self-reported Outcomes of Patients Undergoing Minimally Invasive Lung Cancer Surgery
This study tests if a special nursing program can help patients recover better and faster after minimally invasive lung cancer surgery compared to regular nursing care.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 600 (estimated) |
| Ages | 18 Years to 85 Years |
| Sex | All |
| Sponsor | The Second Hospital of Shandong University Academic / other |
| Locations | 1 site (Jinan, Shandong) |
| Trial ID | NCT05528484 on ClinicalTrials.gov |
What this trial studies
This study evaluates the impact of an Enhanced Recovery After Surgery (ERAS) nursing program on self-reported outcomes for patients undergoing minimally invasive lung cancer surgery. It compares the length of hospital stay, complications, and readmission rates between patients receiving ERAS nursing care and those receiving standard nursing care. The goal is to determine if ERAS nursing can improve recovery metrics for these patients.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 and older who are scheduled for minimally invasive elective lung cancer surgery.
Not a fit: Patients who undergo pneumonectomy that is converted to open surgery or those unable to cooperate due to language barriers or psychological conditions may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved recovery experiences and outcomes for patients undergoing lung cancer surgery.
How similar studies have performed: Other studies have shown positive outcomes with ERAS protocols in various surgical settings, suggesting potential success for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * ≥18years,Minimally invasive elective surgery,cooperate Exclusion Criteria: * Pneumonectomy was performed and converted to open surgery Surgery intensive care, unable to cooperate (language Speech disorders, psychopathology)
Where this trial is running
Jinan, Shandong
- The second hospital of shandong university — Jinan, Shandong, China (Recruiting)
Study contacts
- Study coordinator: ying liu
- Email: liuxia5945@126.com
- Phone: 17660081909
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.