Self-reported Outcomes of Patients in ERAS Nursing

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-85
SponsorThe Second Hospital of Shandong University

About this trial

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

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

≥18years,Minimally invasive elective surgery,cooperate

Disqualifiers

Pneumonectomy was performed and converted to open surgery

Trial design

Design model

Parallel

Treatments tested in this trial

  • ERAS nursing

    Procedure/Surgery

    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

    Procedure/Surgery

    Patients were under the routine management without eras protocol

Treatment groups

600 Participants
are divided into 2 treatment groups
Group A: ERAS groupExperimental treatment 1 intervention
Group B: non-eras groupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Self-reported Outcomes of Patients(PRO)

Use MD Anderson Symptom Checklist - Lung Cancer Symptom to measure severity and functional status

Time frame
at baseline, daily after surgery, and weekly up to 4 after discharge weekly.

Secondary outcomes

1

length of stay (LOS), postoperative cardiopulmonary complications (CPC) and readmission rate (READM)

length of stay (LOS), postoperative cardiopulmonary complications (CPC) and readmission rate (READM)

Time frame
From admission to one month after the patient's discharge

Other outcomes

Sponsors and contacts

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