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Perioperative ERAS Based Nursing Intervention for Laryngeal Cancer Patients

Effect of Perioperative ERAS Based Nursing Intervention on Hope Level of Patients With Laryngeal Cancer

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04174950
Enrollment
200
Registered
2019-11-22
Start date
2018-09-14
Completion date
2020-10-31
Last updated
2019-11-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Laryngeal Cancer, Nursing

Keywords

Laryngeal cancer, enhanced recovery after surgery, hope level

Brief summary

To explore the effect of perioperative ERAS based nursing model on the hope level and recovery of patients with laryngeal cancer.

Detailed description

200 patients who were diagnosed with laryngeal cancer and received total or partial laryngectomy were included. They were allocated into experimental and control group. Patients in experimental group were given ERAS based nursing intervention. Control group were given routine nursing intervention. Compare hope level, postoperative recovery, complication between two groups.

Interventions

routine perioperative nursing intervention, including intensive observation of vital signs, preoperative education, postoperative communication and instruction on diet. NPO after the dinner one day before operation. Patients are instructed to NPO 3 days after surgery and patients should stay on the bed for 3 days. Urinary catheter is always kept for 48 hours or more.

OTHERPerioperative Enhanced Recovery After Surgery (ERAS) Based Nursing Model

Establish ERAS nursing team and formulate ERAS nursing intervention. Nothing by mouth (NPO) 6 hours before operation and no water 4 hours before operation. Patients are given fluid food 24 hours after surgery. Urinary catheter is removed within 24 hours after surgery and encourage patient to mobile 24 hours after surgery. Give support to pain control and psychological support. Intensive observation of vital signs, preoperative education, postoperative communication and instruction on diet were also given to patients.

Sponsors

Second Affiliated Hospital, School of Medicine, Zhejiang University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Intervention model description

Participants were allocated into two groups randomly.

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Patients were confirmed as laryngeal cancer by CT scan. * Patients were given total or partial laryngectomy.

Exclusion criteria

* Unconscious or psychiatric patients. * Patients with distant metastasis or recurrence of cancer * Patients with coagulation dysfunction * Patients with severe cardiac, hepatic or renal dysfunction.

Design outcomes

Primary

MeasureTime frameDescription
Hope levelthe day before surgeryHerth Hope Index which have 12 items. Each item is rated from 1 to 4. Score 1 represents lowest level. Score 4 represents highest level. Total score is 48.

Secondary

MeasureTime frameDescription
Ambulation timeDay 3 after surgeryrecord the time of first ambulation
Level of PainDay 3 after surgeryNumerical rating scale is a common pain rating scale. The score ranges from 0 to 10. 0 is no pain, 10 is the most severe pain.
Postoperative complicationDay 30 after surgeryincidence of infection, malnutrition and Viscosity of sputum
Length of stayDay 30 after surgerythe days of hospitalization

Countries

China

Contacts

Primary ContactXuefei Yu, bachelor
2190049@zju.edu.cn13757119590

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026