Intraoperative Hyperspectral Imaging for Laparoscopic Surgery (NCT06700317) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Intraoperative Hyperspectral Imaging for Laparoscopic Surgery
40 participantsStarted 2025-02-01
Plain-language summary
The study aims to evaluate the use of the HyperSnap Surgical System (HSS1) during laparoscopic surgeries, specifically in bowel resections and cholecystectomies.
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
A) Cholelithiasis or cholecystitis with indications for laparoscopic surgery (cholecystectomy)
* Adult patients aged 18 years and over
* Common bile duct diameter \< 8mm as assessed using ultrasound
* Patients able to provide written informed consent
B) Colorectal cancer requiring elective bowel resection via a laparoscopic approach.
* Adult patients aged 18 years and over
* Patients who are scheduled for elective laparoscopic colon cancer resection
* Patients able to provide written informed consent
Exclusion Criteria:
A) Cholelithiasis or cholecystitis with indications for laparoscopic surgery (cholecystectomy)
* Patients under 18 years of age
* Patients with a history of previous abdominal surgery and multiply scarred abdomen
* Common bile duct diameter ≥ 8mm as assessed using ultrasound
* Patients unable to provide written informed consent
* Patients who are pregnant
B) Colorectal cancer requiring elective bowel resection via a laparoscopic approach.
* Patients under 18 years of age
* Patients with a history of previous abdominal surgery and multiply scarred abdomen
* Patients unable to provide written informed consent
* Patients undergoing emergency surgery
* Patients who are pregnant
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Device safety
Timeframe: From enrollment to end of follow up (30 days)