Non-Small Cell Lung Cancer (NSCLC) Clinical Trial
Official title:
Comparison of Two Techniques of Video Assisted Thoracic Surgery (VATS) Uniportal Lobectomies Through the Transcervical and Standard Intercostal Approaches for Clinical Stage I Non-Small Cell Lung Cancer (NSCLC) in the Prospective Randomized Single-institutional Trial
| NCT number | NCT03997799 |
| Other study ID # | 01/2019 |
| Secondary ID | |
| Status | Recruiting |
| Phase | N/A |
| First received | |
| Last updated | |
| Start date | June 10, 2019 |
| Est. completion date | July 31, 2023 |
Aim of the study is to compare safety and tolerance of two techniques of Video Assisted Thoracic Surgery (VATS) uniportal lobectomies in the prospective randomized single-institutional trial. One arm is a uniportal lobectomy performed through the transcervical approach with elevation of the sternum, the other arm will utilize a standard uniportal intercostal approache. There will be 10 patients in each group. Patients in clinical stage cI-III (T1-3N0-2M0) Non-Small Cell Lung Cancer (NSCLC). The results will be compared for time of the procedure, number of conversions to multi-portal VATS and/or open thoracotomy, duration and volume of chest drainage, amount of postoperatve pain, time of hospitalization and the number of resected lymph nodes and metastatic nodes. Accrual of patients is planned to complete within 12 months.
| Status | Recruiting |
| Enrollment | 20 |
| Est. completion date | July 31, 2023 |
| Est. primary completion date | June 10, 2019 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years to 85 Years |
| Eligibility | Inclusion Criteria: - Patients with histologically, or cytologically proven clinical stage I (cI) NSCLC Exclusion Criteria: - Patients with more advanced NSCLC than clinical stage I (cI) NSCLC - Severe atherosclerotic lesions of the innominate artery and the aortic arch and previous cardiac surgery. - Severe pleural adhesions and calcified intrapulmonary nodes after previous tuberculosis are also technical obstacles for this kind of surgery. |
| Country | Name | City | State |
|---|---|---|---|
| Poland | Pulmonary Hospital | Zakopane |
| Lead Sponsor | Collaborator |
|---|---|
| Pulmonary Hospital Zakopane |
Poland,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | time of the procedure | duration of the operation in minutes | 4 weeks | |
| Primary | number of conversions to multi-portal VATS and/or open thoracotomy | number of conversions to multi-portal VATS and/or open thoracotomy | 4 weeks | |
| Primary | duration of chest drainage | duration of chest drainage in days | 4 weeks | |
| Primary | volume of chest drainage | volume of chest drainage in ml | 4 weeks | |
| Primary | amount of postoperatve pain | 1.pain intensity 0-100 mm VAS scale measured every 4 hours on standard ruler beginning from the end of the surgery.
The visual analogue scale (VAS) is commonly used as the outcome measure for such studies. It is usually presented as a 100-mm horizontal line on which the patient's pain intensity is represented by a point between the extremes of "no pain at all" and "worst pain imaginable." Its simplicity, reliability, and validity, as well as its ratio scale properties, make the VAS the optimal tool for describing pain severity or intensity. |
up to 72 hours after the end of surgery | |
| Primary | time of hospitalization | time of hospitalization in days | 4 weeks | |
| Primary | number of resected lymph nodes | number of resected lymph nodes | 4 weeks | |
| Primary | number of resected metastatic nodes | number of resected metastatic nodes | 4 weeks |
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