Clinical trial · Interventional
Duet TRS Used in Pulmonary Resections
A Prospective, Multi-Center Evaluation of Endo GIA Staplers With Endo GIA Single Use Loading Units (SULUs) With Duet TRS TM in a Pulmonary Resection
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): Sponsor is no longer pursuing this study
Summary
Brief summary (as posted)
The objectives of this clinical trial are to estimate the incidence and duration of air leaks and the incidence of prolonged air leaks (defined as \> 5 days by the Society for Thoracic Surgery) when using the ENDO GIA Staplers with ENDO GIA Single Use Loading Units (SULUs) buttressed with Duet TRS TM in an anatomic pulmonary resection via Video Assisted Thoracoscopic Surgery (VATS). Anatomic pulmonary resection is defined as either a lobectomy or segmental resection. Results of the study will be compared to contemporary literature for a similar population.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Lung Cancer | Malignant Lung Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Duet TRS | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Duet TRS
- description
- This is a single arm study.
- interventionNames
- Device: Duet TRS
Primary outcomes (1)
- measure
- The primary objectives of this clinical trial are to estimate the incidence and duration of air leaks and the incidence of prolonged air leaks (defined as > 5 days)in an anatomic pulmonary resection.
- timeFrame
- intra-operative and 1 month follow up
Secondary outcomes (1)
- measure
- The secondary objectives are length of hospital stay, duration of chest tube following surgery and need for Heimlich valve at discharge.
- timeFrame
- discharge and 1 month follow up
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * The patient must be 18 years of age or older * The patient must be scheduled to undergo segmentectomy or lobectomy via Video Assisted Thoracoscopic Surgery (VATS) for a lung nodule suspicious for or clinically proven to be primary lung cancer * The patient must be able to tolerate general anesthesia and have cardiopulmonary reserve to tolerate the procedure * The patient must be willing and able to comply with all study requirements and have understood and signed the informed consent. Exclusion Criteria: * The patient is pregnant or breastfeeding * The patient is scheduled to undergo sleeve lobectomy, wedge resection, bi-lobectomy, pneumonectomy or Lung Volume Reduction Surgery (LVRS), or lung biopsy for suspected interstitial lung disease * The patient has received pre-operative chemotherapy or radiation therapy for the lung cancer that will be resected * The patient is scheduled to receive intra-operative brachytherapy * The patient has other severe illnesses that would preclude surgery such as unstable angina or myocardial infarction within 3 months * Re-operative surgery is excluded if it is on the same side as the previous surgery * The patient requires chest wall reconstruction
References
Publications (0)
Data not yet available