A Prospective, Single-Arm Multi-Center Study of the HARMONIC® 1100 Shears in Select Devices
Completed · Not applicable
Conditions studied: Pediatric Procedures, Adult Hepato-pancreato-biliary (HPB) Procedures, Adult Lower Gastrointestinal Procedures, Adult Gastric Procedures, Adult Gynecological Procedures, Adult Urological Procedures, Adult Thoracic Procedures
In brief
This prospective, single-arm, multi-center study will collect clinical data in a post-market setting for the pediatric population (general surgical procedures) and adult population (general, gynecological, urological, and thoracic surgical procedures). Investigators will perform each procedure using the device in compliance with their standard surgical approach and the HARMONIC 1100 Shears and Generator G11 instructions for use.
Key facts
- Study ID
- NCT05039021
- Run by
- Ethicon Endo-Surgery
- People needed
- 265
- Starts
- 2021-07-29
- Expected to finish
- 2024-03-12
- Last updated by the study team
- 2025-04-30
Who can join
Age: any. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Pediatric population:
- Non-emergent procedure (general) where at least one vessel is planned to be transected by the HARMONIC 1100 Shears per the IFU;
- Less than 18 years of age at the time of procedure; and
- The subject's parent/legal guardian must be willing to give permission for the subject to participate in the study and provide written informed consent for the subject. In addition, assent must be obtained from pediatric subjects who possess the intellectual and emotional ability to comprehend the concepts involved in the study. If the pediatric subject 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 written informed consent for the subject will be acceptable for the subject to be included in the study.
- Adult population:
- Elective procedure (general, gynecological, urological, or thoracic) where at least one vessel is planned to be transected by the HARMONIC 1100 Shears per the IFU;
- Willingness to give consent and comply with all study-related evaluations and visit schedule; and
- At least 18 years of age.
You may not qualify if…
- Preoperative
- Physical or psychological condition which would impair study participation;
- Female subjects, of childbearing age, who are pregnant; or
- Enrollment in a concurrent interventional clinical study that could impact the study endpoints.
- Intraoperative
- The HARMONIC 1100 Shears were not attempted to be used for at least one single vessel transection during the surgical procedure.
Where it is running
- Baptist Health — Jacksonville, Florida, United States
- Indiana University — Indianapolis, Indiana, United States
- IU Health University Hospital — Indianapolis, Indiana, United States
- Riley Hospital for Children at Indiana University Health — Indianapolis, Indiana, United States
- Centre Hospitalier de l'Universite de Montreal — Montreal, Canada
- Toronto General Hospital — Toronto, Canada
- Western General Hospital — Edinburgh, Scotland, United Kingdom
Full record on ClinicalTrials.gov
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