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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05528484
Other study ID # ERAS (PRO)-based study
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date October 1, 2019
Est. completion date August 31, 2027

Study information

Verified date August 2022
Source The Second Hospital of Shandong University
Contact ying liu
Phone 17660081909
Email liuxia5945@126.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

We aimed to evaluate the effect of ERAS nursing program on self-reported outcomes of patients undergoing minimally invasive lung cancer surgery, and compared the differences in length of hospital stay, complications, and readmission rate between ERAS and non-ERAS nursing programs


Recruitment information / eligibility

Status Recruiting
Enrollment 600
Est. completion date August 31, 2027
Est. primary completion date June 1, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 85 Years
Eligibility 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)

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
ERAS nursing
Patients were given education before surgery, fluid and anesthetic drug management during surgery, early ambulation, fluid management and early feeding after surgery, etc
non eras nursing
Patients were under the routine management without eras protocol

Locations

Country Name City State
China The second hospital of shandong university Jinan Shandong

Sponsors (1)

Lead Sponsor Collaborator
The Second Hospital of Shandong University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Self-reported Outcomes of Patients(PRO) Use MD Anderson Symptom Checklist - Lung Cancer Symptom to measure severity and functional status at baseline, daily after surgery, and weekly up to 4 after discharge weekly.
Secondary length of stay (LOS), postoperative cardiopulmonary complications (CPC) and readmission rate (READM) length of stay (LOS), postoperative cardiopulmonary complications (CPC) and readmission rate (READM) From admission to one month after the patient's discharge
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