Clinical trial · Interventional
VATS Lobectomy for Clinical Stage IB or II Lung Cancer
Feasibility of VATS(Video-Assisted Thoracoscopic Surgery) Lobectomy for Clinical Stage IB or II Non-Small Cell Lung Cancer
NCT00425022CI-TRIAL-00000590unknownPhase 2ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
To examine the feasibility of VATS lobectomy for clinical stage IB or II non-small cell lung cancer. Success is defined as VATS lobectomy without conversion. If success rate over 90%, VATS lobectomy is considered as feasible procedures for clinical stage IB or II non-small cell lung cancer
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Carcinoma, Non-Small-Cell Lung | Lung Non-Small Cell Carcinoma | ALIAS | 0.90 |
| Thoracic Surgery, Video-Assisted | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| thoracoscopy | Procedure | — | UNRESOLVED |
Design
Arms and outcomes
Arms (0)
[]Primary outcomes (3)
- measure
- To examine the feasibility of VATS lobectomy for clinical stage IB or II non-small cell lung cancer.
- measure
- Success is defined as VATS lobectomy without conversion.
- measure
- If success rate over 90%, VATS lobectomy is considered as feasible procedures for clinical stage IB or II non-small cell lung cancer
Secondary outcomes (5)
- measure
- To evaluate the number of dissected lymph nodes and the rate of contamination during lymph node dissection according to the lymph node stations under VATS
- measure
- To estimate the reccurrence rate (locoregional and distant metastasis)
- measure
- To estimate the overall survival
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 80 Years
Show eligibility criteria text
Inclusion Criteria: 1. Histologic or cytologic diagnosis of non-small cell lung cancer. 2. Clinical stage IB or II, according to the American Joint Committee on Cancer (AJCC). 3. Tumor ≤ 6 cm in size amenable to surgical resection. 4. Including clinical IB or II NSCLC after neoadjuvant therapy 5. Performance status of 0-1 on ECOG scale. 6. At least 18 years old. 7. Patient compliance that allows adequate follow-up. 8. Medical fitness of patients adequate for radical NSCLC surgery. 9. Adequate organ function including the following:Adequate hematologic function: WBC count ³ 4,000/uL, absolute neutrophil count (ANC) ³ 1,500/uL, platelet count ³ 100,000/uL, and hemoglobin ³ 10 gm/dL.Adequate hepatic function: bilirubin £ 1.5 x UNL, ALT or AST £ 2.5 x UNL.Adequate renal function: creatinine £ 1.5mg/dL. 10. Signed informed consent from patient or legal representative. 11. Patients with reproductive potential must use an approved contraceptive method during and for 3 months after the study. Females with childbearing potential must have a negative urine hCG test within 7 days prior to study enrollment. Exclusion Criteria: 1. Metastatic disease in workup 2. Any T3, T4 lesion or N2, N3 lesion 3. Concurrent administration of other tumor therapy, including radiotherapy, immunotherapy except chemotherapy. 4. Active uncontrolled infection. 5. Serious concomitant disorders that would compromise the safety of patient or compromise the patient's ability to tolerate therapy. 6. Significant neurological or mental disorder. 7. Previous history of malignancy in any organ 8. Pregnant or nursing.
References
Publications (0)
Data not yet available
No reference posted for this study.