NCT07660900 Evaluating the Association of Force Feedback With Outcomes After Lung Resection Using the da Vinci Multiport System
| NCT ID | NCT07660900 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Ohio State University |
| Condition | Lobectomy |
| Study Type | OBSERVATIONAL |
| Enrollment | 270 participants |
| Start Date | 2025-09-05 |
| Primary Completion | 2027-06-30 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.
This trial targets 270 participants in total. It began in 2025-09-05 with a primary completion date of 2027-06-30.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
The purpose of this research is to study patient outcomes based on the use of Force Feedback instruments during robotic-assisted lung resection. Force Feedback technology describes the physical forces a surgeon senses when pushing and pulling structures inside the body during robotic-assisted surgery.
Eligibility Criteria
Inclusion Criteria: * Ages 18 years or older * Undergoing robotic-assisted anatomic lung resection (lobectomy or segmentectomy) at The Ohio State University Wexner Medical Center Exclusion Criteria: * Age \< 18 years old * Subject is pregnant or suspected to be pregnant or breastfeeding * ECOG Performance status \> 2 * Do not qualify for ERAS protocol * Undergoing an emergent procedure * Undergoing non-anatomic lung resection * Undergoing pneumonectomy * Previous ipsilateral thoracic surgery (open, video-assisted thoracoscopic or robotic) * Planned to undergo major concomitant surgery for the treatment of a different medical condition than was originally planned * Non-English speaking
Frequently Asked Questions
Who can join the NCT07660900 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, studying Lobectomy. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07660900 currently recruiting?
Yes, NCT07660900 is actively recruiting participants. Visit ClinicalTrials.gov or contact Ohio State University to inquire about joining.
Where is the NCT07660900 trial being conducted?
This trial is being conducted at Columbus, United States.
Who is sponsoring the NCT07660900 clinical trial?
NCT07660900 is sponsored by Ohio State University. The trial plans to enroll 270 participants.