Clinical trial · Observational
Use of a New Stapling Device in General Thoracic Surgery
NCT05143541CI-TRIAL-00062941completedResults postedClinicalTrials.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)
The goal of this study was to test the safety and efficacy of this stapler in our general thoracic surgery practice.
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 |
|---|---|---|---|
| Thoracic Cancer | Malignant Thoracic Neoplasm | ALIAS | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| AEON Endostapler | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- label
- AEON Endostapler
- description
- Stapling performed with AEON Endostapler
- interventionNames
- Device: AEON Endostapler
Primary outcomes (3)
- measure
- Number of Participants With Product Malfunction
- timeFrame
- Within surgery, up to 8 hours
- description
- Number of participants with product malfunction. Product malfunction means any occurrence during the surgery where the stapler does not perform as intended.
- measure
- Number of Participants With Intraoperative Staple Line Bleeding
- timeFrame
- Within surgery, up to 8 hours
- description
- Number of participants with intraoperative staple line bleeding
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Patients undergoing planned VATS or open lung resection surgery (lobectomy or wedge resection) Exclusion Criteria: * Active bacterial or fungal infection * Prior history of VATS or open lung surgery * Use of staple line reinforcement material (buttress) * Patients under the age of 18 on the date of the surgery * Any female patient who is pregnant * Scheduled concurrent surgical procedure other than lobectomy or wedge resection (central venous access - e.g., port placement, mediastinoscopy with lymph node sampling, and VATS lymphadenectomy are allowed)
References
Publications (0)
Data not yet available
No reference posted for this study.