Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Ethicon Endo-Surgery
Age
Any age
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Adult and pediatric participants satisfying the following criteria will be considered eligible for enrollment in this study (procedures may be performed with or without a robot): Primary procedure where the ECHELON 3000 Stapler and reload system is planned to be used for tissue transection per the instructions for use (IFU) in either of the following, a) Laparoscopic Sleeve Gastrectomy; b) Lung resection procedures (VATS or open)
Adult participants- Willingness to give consent and comply with all study-related evaluations and visit schedule
Pediatric participants- The participant's parent/legal guardian must be willing to give permission for the participant to participate in the study and provide documented informed consent for the participants. In addition, assent must be obtained from pediatric participant who possess the intellectual and emotional ability to comprehend the concepts involved in the study. If the pediatric participant is not able to provide assent (due to age, maturity and/or inability to intellectually and/or emotionally comprehend the study), the parent/legal guardian's documented informed consent for the participant will be acceptable for the participant to be included in the study
You may not be if
Physical or psychological condition which would impair study participation
Procedure is a revision/reoperation for the same indication or same anatomical location
A procedure where surgical stapling is contraindicated
Concurrent treatment with medications that the investigator deems could have influence on wound healing
Enrollment in a concurrent interventional clinical study that could impact the study endpoints
