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Group-Based Trajectory Risk Assessment of Postoperative Prolonged Air Leak and Evaluation of a Precision Nursing Intervention Model

Group-Based Trajectory Risk Assessment of Postoperative Prolonged Air Leak and Evaluation of a Precision Nursing Intervention Model

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500115810
Enrollment
Unknown
Registered
2025-12-31
Start date
2026-01-01
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Persistent lung leakage

Interventions

Precision Nursing Group:Trajectory-based Precision Nursing Intervention
Usual Care Group:Standard Perioperative Nursing Care

Sponsors

Zhejiang Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Age: 18-80 years old, gender not limited. 2. Primary lung cancer is confirmed by histopathology or highly suspected. 3. Plan to undergo elective lobectomy (single or double lobectomy; thoracotomy or thoracoscopy are both acceptable); 4. It is expected that the digital thoracic drainage system will be connected after the operation (the thoracic tube should be left in place for more than 24 hours during the cohort stage). 5. Preoperative cardiopulmonary function assessment shows that the patient can tolerate the surgery. 6. The patient or their legal representative signs the informed consent form; 7. Be able to cooperate with the implementation of nursing intervention and follow-up.

Exclusion criteria

Exclusion criteria: 1. Previous history of ipsilateral chest surgery or pleural diseases; 2. Preoperative active thoracic infection/empyema or a large amount of pleural effusion; 3. Extensive pleural dissemination was found during the operation, and it needs to be changed to palliative surgery. 4. Combined with severe cognitive impairment/mental illness/communication disorders, unable to cooperate; 5. End-stage patients with an expected survival period of less than 3 months (measured in the RCT stage); 6. Participate in other clinical trials simultaneously; 7. Other circumstances where the researcher determines that enrollment is not suitable; 8. (Supplementary in the cohort stage) Perioperative death (within 30 days after surgery) or absence of key variables >50% / equipment failure resulting in data inability to obtain.

Design outcomes

Primary

MeasureTime frame
Incidence of Prolonged Air Leak;

Secondary

MeasureTime frame
Total length of hospital stay;Lung Re-expansion;Postoperative pain score;Duration of Chest Tube Placement;

Countries

China

Contacts

Public ContactQuan Yiping

Zhejiang Cancer Hospital

1836763015@qq.com+86 10 88128061

Outcome results

None listed

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