Clinical value of enhanced recovery after surgery and early enteral nutrition in patients with non-small cell lung cancer after surgery

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR1900027711

Enrollment

Unknown

Registered

2019-11-24

Start date

2019-12-01

Completion date

Unknown

Last updated

2019-11-25

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

Conditions

non-small cell lung cancer

Interventions

EEN group:early enteral nutrition

Control group:No intervention

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) aged >=18 years; (2) cough symptom not experienced within 2 weeks prior to surgery; (3) provided signed informed consent; (4) underwent surgery performed via video-assisted thoracic surgery (VATS); (5) postoperative pathological findings indicative of NSCLC.

Exclusion criteria

Exclusion criteria: (1) conversion to thoracotomy or bleeding of over 1000 ml; (2) underwent pneumonectomy; (3) transfered to ICU after surgery; (4) Receiving preoperative neoadjuvant therapy such as chemotherapy, radiotherapy or immunization; (5) rejected survey or dropped out; (6) lung cancer TNM stage of pT4, pN3 and/or M1.

Design outcomes

Primary

Measure	Time frame
MDASI-LC;numerical rating scale;	—

Countries

China

Contacts

Public ContactPan Xiaojie

Fujian Provincial Hospital

rongjia.lin@163.com+86 0591-87557768

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026