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A prospective randomized controlled trial of the comparison of the effect of postoperative pain management of HilumDirect uVATS and conventional uVATS

A prospective randomized controlled trial of the comparison of the effect of postoperative pain management of HilumDirect uVATS and conventional uVATS

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600125345
Enrollment
Unknown
Registered
2026-05-26
Start date
2026-06-01
Completion date
Unknown
Last updated
2026-06-01

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

Trial group:Received HilumDirect uVATS for radical resection of NSCLC
Control group:Received conventional uVATS for radical resection of NSCLC

Sponsors

Peking University First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 79 Years

Inclusion criteria

Inclusion criteria: Primary Inclusion Criteria: 1. Age between 18 and 79 years; 2. Patients with lung cancer requiring radical pulmonary resection; 3. Eastern Cooperative Oncology Group (ECOG) performance status score of 0 or 1; 4. Suspected pulmonary malignancy based on chest computed tomography (CT) or positron emission tomography-CT (PET-CT) scans; 5. Peripheral tumors, defined as tumors located at or distal to the opening of the segmental bronchus; 6. Primary pulmonary tumor without invasion or metastasis to other lung lobes; 7. Preoperative clinical stage T1-3N0-1M0 (according to the 9th edition of the AJCC/UICC TNM staging system), excluding the following types: (1) Cases with involvement of vital organs such as the diaphragm, superior vena cava, or spine; (2) cN1 cases with extranodal extension (CT scan indicating invasion of adjacent bronchi or pulmonary vessels); 8. No previous history of surgery for thoracic malignancies; 9. No prior neoadjuvant radiotherapy, neoadjuvant chemotherapy, or neoadjuvant chemoradiotherapy, and no prior administration of targeted therapy or immunotherapy drugs (a history of chemotherapy or hormonal therapy for malignancies in other parts of the body is permissible); 10. Predicted postoperative forced expiratory volume in 1 second (FEV1) >= 800 ml; 11. American Society of Anesthesiologists (ASA) physical status classification of I to III. Secondary Inclusion Criteria: 1. Surgery performed within 14 days after the initial assessment confirming eligibility based on the primary inclusion criteria; 2. Intraoperative confirmation of the feasibility of radical resection; 3. No intraoperative evidence of malignant pleural effusion or intrathoracic dissemination.

Exclusion criteria

Exclusion criteria: 1. Synchronous double or multiple tumors, or metachronous double or multiple metastatic tumors; 2. Pulmonary tumors requiring pneumonectomy for radical resection; 3. Presence of an active infection requiring systemic antimicrobial therapy; 4. Severe psychiatric disorders; 5. Currently receiving or having recently (within 2 weeks) received continuous corticosteroid or immunosuppressive therapy; 6. Hypertension or diabetes mellitus uncontrolled by systemic medical treatment; 7. A history of severe heart disease, heart failure, or myocardial infarction within the past 6 months, or confirmed episodes of angina pectoris within the past 6 months; 8. Interstitial lung disease, pulmonary fibrosis, or severe emphysema; 9. Postoperative pathological confirmation of lesions other than non-small cell lung cancer (NSCLC).

Design outcomes

Primary

MeasureTime frame
NRS score;

Secondary

MeasureTime frame
Chronic pain;

Countries

China

Contacts

Public ContactZHANG XINING

Peking University First Hospital

xining_bdyy@163.com+86 185 0052 8993

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026