CholecystitisNCT05775133
Feasibility and Utility of Artificial Intelligence (AI) / Machine Learning (ML) - Driven Advanced Intraoperative Visualization and Identification of Critical Anatomic Structures and Procedural Phases in Laparoscopic Cholecystectomy
A study testing ICG in people with Cholecystitis and Cholelithiasis, run by Activ Surgical at 1 site in United States.
Trial summary
The goal of this study is to evaluate the utility and efficacy of an artificial intelligence (AI) model at identifying structures and phases of surgery compared to traditional white light assessment by trained surgeons. Read more about this study
- Who is it for?
- Ages 18 years and olderHealthy volunteers can take part
- Conditions the study is for
- Cholecystitis, Cholelithiasis, Biliary Dyskinesia
- What is being tested?
- ICG
- Type of treatment
- Injection or infusion, Medical device
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 120 participants
- Where
- 1 siteUnited States
- Study dates
- 1 Aug 2023to Dec 2025
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- All patients age > 18 years old who are planned for elective laparoscopic cholecystectomy; spoken command and literacy in the native language spoken at each participating center; ability to understand and follow study procedures; and having provided signed consent.
- Eligible patients will be screened and assigned as per risk calculator for difficulty of LC
- Diagnosis:
- All patients with clinical suspicion and diagnosis of symptomatic cholelithiasis or cholecystitis planned for cholecystectomy.
- Typical imaging as per standard workup findings including US, CT and/or MRI. Plain radiographs and contrast imaging may be obtained by referring physicians and are helpful for confirming the clinical diagnosis.
- Prior therapy:
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- o Patients with prior surgery are eligible for enrollment.
- Laboratory:
- Hemoglobin > 9 g/dL
- Platelet count ≥75,000/µL (may receive transfusions)
- Normal prothrombin time (PT), partial thromboplastin time (PTT) and international normalized ratio (INR) < 1.5 x upper limit of normal (including patients on prophylactic anticoagulation)
- Liver Function Test
- Renal function: Age-adjusted normal serum creatinine
- Adequate pulmonary function: Defined as no dyspnea at rest, and a pulse oximetry >94% on room air if there is any clinical indication for determination.
Who cannot join
- Non-elective acute cholecystectomy will be excluded.
- Patients assigned to FDA cleared ICG-based visualization are contraindicated for any chronic renal dysfunction, potential drug interaction, history of allergy to ICG or anaphylaxis, and pregnancy.
- Patients eligible for cholecystectomy, exclusion criteria include known allergy to ICG; coagulopathy or known, pre-existing liver disease; pregnancy or breast-feeding; or being of reproductive age with pregnancy possible and not ruled out.
- Patients currently in any investigational agents.
- Adults unable to consent
- Individuals under 18 years of age
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- Pregnant women
- Prisoners
- Vulnerable populations
Trial locations and contacts
1 site in 1 country.
United States1 site, 1 recruiting
- Recruiting
Memorial Hermann Texas Medical Center
Houston, Texas, 77030
Connie Klein, APRN, CBN, 713-486-1338, Connie.Pollard@uth.tmc.edu
Angielyn R Rivera, (713) 486 1350, Angielyn.R.Rivera@uth.tmc.edu
About this study
The goal of this study is to evaluate the utility and efficacy of an artificial intelligence (AI) model at identifying structures and phases of surgery compared to traditional white light assessment by trained surgeons. Surgeons will perform the procedure in their standard practice, while the AI model analyzes data from the laparoscopic camera. Surgeons will be asked to audibly state when they identify structures and enter different phases of the surgical procedure.
The AI will not alter the surgeon's view or be visible to the surgeon, and the surgeon will perform the procedure in the exact same fashion as they typically do.
Read the detailed description
Bile duct injury (BDI) during cholecystectomy is a serious surgical complication with increased risk of early death, serious ongoing morbidities including multiple reinterventions requiring prolonged and repeated hospital stay, and over a billion dollars in additional healthcare costs in US each year. The introduction laparoscopic approach has progressively increased overall laparoscopic cholecystectomy procedure volume, for clearly proven benefits of minimally invasive approach. However, despite the benefits, minimally invasive approach has resulted in increased and persistent incidence of BDI up to 4-folds in some reports.
Most major biliary injuries result from unrecognized or unintended perception, either misidentification or misinterpretation of the common bile or hepatic duct as the cystic duct or misidentification of an aberrant bile duct. It is increasingly clear that the routine use of intraoperative cholangiography (IOC) has a significant association with decreased and earlier intraoperative detection of BDI. The recent 'state of the art consensus conference on prevention of bile duct injury during cholecystectomy' in 2018 strongly recommended that documenting the critical view of safety (CVoS) and a liberal use of IOC in anticipated difficult cholecystectomy are highly recommended steps that can potentially mitigate the risk of BDI during laparoscopic cholecystectomy (LC) in patients especially with uncertain anatomy or difficult dissection.
Performing traditional IOC laparoscopically under fluoroscopic guidance however can challenge surgeons' skills, is time-consuming, and requires a learning curve to interpret images. Despite well-known and accepted risk factors for difficult cholecystectomies and potential for BDI, the use of advanced imaging for IOC however remains variable and highly user dependent. The rationale for selective use of IOC is attributable to the fact that the prevalence and incidence of BDI are low that an individual practitioner would infrequently encounter such complication in their daily practice or lifetime of a surgeon to justify a routine use. This is further compounded by the fact that radiation-based fluoroscopic IOC are cumbersome to efficient workflow, utility and cost (need for contrast reagent preparation and injection, potential adverse allergic reactions, risk of radiation exposure, training requirement, need for large capital equipment, space and cost), and variability in proficient analysis.
Recent randomized controlled trials using near-infrared fluorescent cholangiography (NIFC) using indocyanine green (ICG) demonstrated significantly superior visualization of extrahepatic biliary structures during laparoscopic cholecystectomy to white light (WLI) alone. Pre-dissection surgeon detection rates on naked eye were significantly higher (> 1.8 - 3.1 folds) with NIFC use for all 7 biliary structures than traditional WLI alone. However, although similar intergroup differences were observed for all structures, addition of NIFC did not improve additional detection of cystic duct and cystic duct/gallbladder junction after dissection has been done. In addition, increased body mass index was associated with reduced detection of most structures in both groups, especially before dissection. Interestingly, only 2 patients, both in the WLI group, sustained a biliary duct injury.
ActivSightTM is an FDA-cleared device that combines ICG fluorescence for extrahepatic biliary visualization and laser speckle contrast imaging (LSCI) for perfusion detection in a laparoscopic form factor. ActivSightTM allows augmented visualization to any current WLI laparoscopic visualization system displaying both extrahepatic biliary ICG and microperfusion over cystic duct and artery. As a non-significant risk device, ActivSightTM has been used in well over 150 patients for laparoscopic cholecystectomies and bariatric, esophageal, and colorectal procedures, with proven safety and utility. Moreover, ActivSightTM allows raw infrared visualization data for advanced analysis and AI/ML model development.
Surgeons/scientists now have segmented and analyzed different procedural phases of LC, and developed inferencing models and algorithms using artificial intelligence (AI)/machine learning (ML) based on standard WLI procedural videos. Although AI/ML models recognizing different phases of LC procedures can be as accurate as 80-95% on limited trained dataset once structures have been clearly dissected, more relevant and key value would be in identifying critical structures such as bile ducts and arteries before and during, not after surgical dissection has been performed. Early detection and identification of these critical structures before and during dissection of the triangle based on AI/ML trained on computer vision may aid surgeons in performing more effective and safer LC.
ActivSightTM is an FDA 510(k)-cleared optical imaging system based on monochromatic coherent light known as Laser-speckle-contrast imaging (LSCI) and represents a label-free imaging method using coherent monochromatic light where blood flow and tissue perfusion can be detected. A small imaging module that fits between any existing laparoscope and camera systems and a separate light source placed along any current commercial system will deliver objective real-time tissue perfusion and blood flow information intraoperatively. In addition, ActivSightTM can also effectively display with push of button an ICG-based visualization of the biliary tree in real time at equivalent or superior to current commercial products. The innovative form factor of ActivSight enables any laparoscopic system for ICG-based visualization at a fraction of the cost of current competitor with minimal disruption to workflow.
ActivInsightTM is a prototype software feature in ActivSightTM that recognizes procedural phases and critical anatomic structures, namely gallbladder, cystic duct, and cystic artery during LC using AI/ML-based algorithms. The key difference of ActivInsightTM to other models reported in the literature is that ActivInsightTM is trained on dataset annotated using ICG and LSCI in addition to WLI.
In this trial, the investigators propose to first validate and then test the precision and accuracy of ActivInsightTM in detecting critical phases and structures and compare the performance of the algorithms to those based on models developed using WLI only and traditional surgeon's naked eye detection during LC in pre-and mid-dissection phases. To eliminate any bias, the investigators will connect a secondary screen blinded to the main operating surgeon screens so that real-time function of the AI/ML is not visible to operating surgeons, to perform real-time analysis and comparison of routine use of advanced augmented visualization versus current WLI visualization alone with or without computer vision-based AI/ML.
- Conditions
- Cholecystitis, Cholelithiasis, Biliary Dyskinesia
- Being tested
- ICG
- Keywords
- artificial intelligence, laparoscopy, laparoscopic surgery
- Medical subject headings
- Cholecystitis, Cholelithiasis, Biliary Dyskinesia
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
ICGDevice
Patient will receive a standard dose of indocyanine green (ICG) 45 minutes prior to surgery. ActivSight will be used during laparoscopic cholecystectomy - the surgeon will perform the procedure in their standard fashion.
Video data will be analyzed in real-time by Activ Surgical's ActivInsight surgical artificial intelligence platform to identify anatomic structures and surgical phase. The surgeon will be blinded to this information, and will see the standard screens and information they do when performing the procedure in a non-study setting.
| Study group | Role | What they receive |
|---|---|---|
| Indocyanine green (ICG) | Experimental | Patients in this arm will receive an intravenous injection of indocyanine green (ICG) 45 minutes prior to the start of surgery. This will be used to visualize the biliary anatomy using ActivSight, a device that is FDA 510(k)-cleared for this indication.
The surgeon will perform the procedure in their standard fashion using ActivSight.
ActivInsight artificial intelligence will be used to analyze the surgical video in real time to identify anatomic structures and phases of surgery. Receives: Device: ICG |
| Non-Indocyanine Green (Non-ICG) | No intervention | The surgeon will perform the procedure in their standard fashion without the use of ICG. ActivInsight artificial intelligence will be used to analyze the surgical video in real time to identify anatomic structures and phases of surgery. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Precision and accuracy
Precision and accuracy of AI/ML model at identifying procedural phases and critical anatomic structures in laparoscopic cholecystectomy (LC).
Precision will be calculated as True Positives / (True Positives + False Positives)
Accuracy will be calculated as (True Positives + True Negatives) / Total Samples
"True Positive" will be when the AI correctly identifies a procedural phase or critical anatomic structure. "False Positive" will be when it incorrectly labels a procedural phase or critical anatomic structure as the phase or structure of interest. "True Negatives" will be when the AI model correctly labels the phase or structure as not the label of interest.
Accuracy and precision will be determined for each of the following labels:
- each of three procedural phases (pre-, intra-, and post-gallbladder dissection)
- each of seven biliary structures: gallbladder, cystic duct, common hepatic duct, common bile duct, cystic artery, region of interest, danger zone
Measured: Immediately after each procedure
Secondary outcomes (4)
Length of procedure
Augmented display of the critical anatomic structures and procedural phases using indocyanine green (ICG) and laser speckle contrast imaging (LSCI) may detect the structures and procedural phases earlier than LC performed using standard WLI display alone
Measured: Immediately after each procedure
Conversion rate to open procedure
Routine augmented visualization and identification of the critical phases and structures may potentially reduce current conversion rate.
Measured: Immediately after each procedure
Complication rate
Comparison of complication rate between augmented visualization and WLI groups
Measured: One month after each procedure
Length of hospital stay
Comparison of hospital stay length between augmented visualization and WLI groups
Measured: One month after each procedure
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted20 Mar 2023
- Study start1 Aug 2023
- Primary completionDec 2025 (estimated)
- Study completionDec 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for CholecystitisStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Diagnosis
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 120 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Activ Surgical
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Peter Kim, MD, PhD, Principal investigator, Activ Surgical
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05775133
- Sponsor's protocol ID
- 20220620
- Status last verified
- Feb 2024
- First submitted
- 23 Feb 2023
- Last updated
- 21 Feb 2024
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- Yes
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 21 Feb 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Feasibility and Utility of Artificial Intelligence (AI) / Machine Learning (ML) - Driven Advanced Intraoperative Visualization and Identification of Critical Anatomic Structures and Procedural Phases in Laparoscopic Cholecystectomy
- ClinicalTrials.gov ID
- NCT05775133
- Acronym / sponsor ID
- 20220620
- Conditions
- Cholecystitis, Cholelithiasis, Biliary Dyskinesia
- Keywords
- artificial intelligence, laparoscopy, laparoscopic surgery
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 120 participants (estimated)
- Lead sponsor
- Activ SurgicalIndustry (pharma, biotech, devices)
- Study start
- 1 Aug 2023 (actual)
- Primary completion
- Dec 2025 (estimated)
- Study completion
- Dec 2025 (estimated)
- First posted
- 20 Mar 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The goal of this study is to evaluate the utility and efficacy of an artificial intelligence (AI) model at identifying structures and phases of surgery compared to traditional white light assessment by trained surgeons. Surgeons will perform the procedure in their standard practice, while the AI model analyzes data from the laparoscopic camera. Surgeons will be asked to audibly state when they identify structures and enter different phases of the surgical procedure.
The AI will not alter the surgeon's view or be visible to the surgeon, and the surgeon will perform the procedure in the exact same fashion as they typically do.
Detailed description
Bile duct injury (BDI) during cholecystectomy is a serious surgical complication with increased risk of early death, serious ongoing morbidities including multiple reinterventions requiring prolonged and repeated hospital stay, and over a billion dollars in additional healthcare costs in US each year. The introduction laparoscopic approach has progressively increased overall laparoscopic cholecystectomy procedure volume, for clearly proven benefits of minimally invasive approach. However, despite the benefits, minimally invasive approach has resulted in increased and persistent incidence of BDI up to 4-folds in some reports.
Most major biliary injuries result from unrecognized or unintended perception, either misidentification or misinterpretation of the common bile or hepatic duct as the cystic duct or misidentification of an aberrant bile duct. It is increasingly clear that the routine use of intraoperative cholangiography (IOC) has a significant association with decreased and earlier intraoperative detection of BDI. The recent 'state of the art consensus conference on prevention of bile duct injury during cholecystectomy' in 2018 strongly recommended that documenting the critical view of safety (CVoS) and a liberal use of IOC in anticipated difficult cholecystectomy are highly recommended steps that can potentially mitigate the risk of BDI during laparoscopic cholecystectomy (LC) in patients especially with uncertain anatomy or difficult dissection.
Performing traditional IOC laparoscopically under fluoroscopic guidance however can challenge surgeons' skills, is time-consuming, and requires a learning curve to interpret images. Despite well-known and accepted risk factors for difficult cholecystectomies and potential for BDI, the use of advanced imaging for IOC however remains variable and highly user dependent. The rationale for selective use of IOC is attributable to the fact that the prevalence and incidence of BDI are low that an individual practitioner would infrequently encounter such complication in their daily practice or lifetime of a surgeon to justify a routine use. This is further compounded by the fact that radiation-based fluoroscopic IOC are cumbersome to efficient workflow, utility and cost (need for contrast reagent preparation and injection, potential adverse allergic reactions, risk of radiation exposure, training requirement, need for large capital equipment, space and cost), and variability in proficient analysis.
Recent randomized controlled trials using near-infrared fluorescent cholangiography (NIFC) using indocyanine green (ICG) demonstrated significantly superior visualization of extrahepatic biliary structures during laparoscopic cholecystectomy to white light (WLI) alone. Pre-dissection surgeon detection rates on naked eye were significantly higher (> 1.8 - 3.1 folds) with NIFC use for all 7 biliary structures than traditional WLI alone. However, although similar intergroup differences were observed for all structures, addition of NIFC did not improve additional detection of cystic duct and cystic duct/gallbladder junction after dissection has been done. In addition, increased body mass index was associated with reduced detection of most structures in both groups, especially before dissection. Interestingly, only 2 patients, both in the WLI group, sustained a biliary duct injury.
ActivSightTM is an FDA-cleared device that combines ICG fluorescence for extrahepatic biliary visualization and laser speckle contrast imaging (LSCI) for perfusion detection in a laparoscopic form factor. ActivSightTM allows augmented visualization to any current WLI laparoscopic visualization system displaying both extrahepatic biliary ICG and microperfusion over cystic duct and artery. As a non-significant risk device, ActivSightTM has been used in well over 150 patients for laparoscopic cholecystectomies and bariatric, esophageal, and colorectal procedures, with proven safety and utility. Moreover, ActivSightTM allows raw infrared visualization data for advanced analysis and AI/ML model development.
Surgeons/scientists now have segmented and analyzed different procedural phases of LC, and developed inferencing models and algorithms using artificial intelligence (AI)/machine learning (ML) based on standard WLI procedural videos. Although AI/ML models recognizing different phases of LC procedures can be as accurate as 80-95% on limited trained dataset once structures have been clearly dissected, more relevant and key value would be in identifying critical structures such as bile ducts and arteries before and during, not after surgical dissection has been performed. Early detection and identification of these critical structures before and during dissection of the triangle based on AI/ML trained on computer vision may aid surgeons in performing more effective and safer LC.
ActivSightTM is an FDA 510(k)-cleared optical imaging system based on monochromatic coherent light known as Laser-speckle-contrast imaging (LSCI) and represents a label-free imaging method using coherent monochromatic light where blood flow and tissue perfusion can be detected. A small imaging module that fits between any existing laparoscope and camera systems and a separate light source placed along any current commercial system will deliver objective real-time tissue perfusion and blood flow information intraoperatively. In addition, ActivSightTM can also effectively display with push of button an ICG-based visualization of the biliary tree in real time at equivalent or superior to current commercial products. The innovative form factor of ActivSight enables any laparoscopic system for ICG-based visualization at a fraction of the cost of current competitor with minimal disruption to workflow.
ActivInsightTM is a prototype software feature in ActivSightTM that recognizes procedural phases and critical anatomic structures, namely gallbladder, cystic duct, and cystic artery during LC using AI/ML-based algorithms. The key difference of ActivInsightTM to other models reported in the literature is that ActivInsightTM is trained on dataset annotated using ICG and LSCI in addition to WLI.
In this trial, the investigators propose to first validate and then test the precision and accuracy of ActivInsightTM in detecting critical phases and structures and compare the performance of the algorithms to those based on models developed using WLI only and traditional surgeon's naked eye detection during LC in pre-and mid-dissection phases. To eliminate any bias, the investigators will connect a secondary screen blinded to the main operating surgeon screens so that real-time function of the AI/ML is not visible to operating surgeons, to perform real-time analysis and comparison of routine use of advanced augmented visualization versus current WLI visualization alone with or without computer vision-based AI/ML.
Study design
- Primary purpose
- Diagnosis
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Indocyanine green (ICG) | Experimental | Device: ICGPatients in this arm will receive an intravenous injection of indocyanine green (ICG) 45 minutes prior to the start of surgery. This will be used to visualize the biliary anatomy using ActivSight, a device that is FDA 510(k)-cleared for this indication. The surgeon will perform the procedure in their standard fashion using ActivSight. ActivInsight artificial intelligence will be used to analyze the surgical video in real time to identify anatomic structures and phases of surgery. |
| Non-Indocyanine Green (Non-ICG) | No intervention | –The surgeon will perform the procedure in their standard fashion without the use of ICG. ActivInsight artificial intelligence will be used to analyze the surgical video in real time to identify anatomic structures and phases of surgery. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (14 listed)
- All patients age > 18 years old who are planned for elective laparoscopic cholecystectomy; spoken command and literacy in the native language spoken at each participating center; ability to understand and follow study procedures; and having provided signed consent.
- Eligible patients will be screened and assigned as per risk calculator for difficulty of LC
- Diagnosis:
- Prior therapy:
- o Patients with prior surgery are eligible for enrollment.
Key exclusion criteria (9 listed)
- Non-elective acute cholecystectomy will be excluded.
- Patients assigned to FDA cleared ICG-based visualization are contraindicated for any chronic renal dysfunction, potential drug interaction, history of allergy to ICG or anaphylaxis, and pregnancy.
- Patients eligible for cholecystectomy, exclusion criteria include known allergy to ICG; coagulopathy or known, pre-existing liver disease; pregnancy or breast-feeding; or being of reproductive age with pregnancy possible and not ruled out.
- Patients currently in any investigational agents.
- Adults unable to consent
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| ICGPatient will receive a standard dose of indocyanine green (ICG) 45 minutes prior to surgery. ActivSight will be used during laparoscopic cholecystectomy - the surgeon will perform the procedure in their standard fashion. Video data will be analyzed in real-time by Activ Surgical's ActivInsight surgical artificial intelligence platform to identify anatomic structures and surgical phase. The surgeon will be blinded to this information, and will see the standard screens and information they do when performing the procedure in a non-study setting. | Device | Indocyanine green (ICG) |
Primary outcome
Precision and accuracy
Time frame: Immediately after each procedure
Precision and accuracy of AI/ML model at identifying procedural phases and critical anatomic structures in laparoscopic cholecystectomy (LC). Precision will be calculated as True Positives / (True Positives + False Positives) Accuracy will be calculated as (True Positives + True Negatives) / Total Samples "True Positive" will be when the AI correctly identifies a procedural phase or critical anatomic structure. "False Positive" will be when it incorrectly labels a procedural phase or critical anatomic structure as the phase or structure of interest. "True Negatives" will be when the AI model correctly labels the phase or structure as not the label of interest. Accuracy and precision will be determined for each of the following labels: * each of three procedural phases (pre-, intra-, and post-gallbladder dissection) * each of seven biliary structures: gallbladder, cystic duct, common hepatic duct, common bile duct, cystic artery, region of interest, danger zone
4 secondary outcomes
Length of procedure
Time frame: Immediately after each procedure
Conversion rate to open procedure
Time frame: Immediately after each procedure
Complication rate
Time frame: One month after each procedure
Length of hospital stay
Time frame: One month after each procedure
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 21 Feb 2024.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Peter Kim, MD, PhD principal investigator
Activ Surgical
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing ICG in people with Cholecystitis and Cholelithiasis, run by Activ Surgical at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 14 inclusion and 9 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 21 Feb 2024. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Christopher McCulloh, MD (617-333-8162, cmcculloh@activsurgical.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Precision and accuracy (time frame: Immediately after each procedure). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 21 Feb 2024.