Lung NeoplasmsPhase 1/2NCT05346380
Near-Infrared Perfusion During Minimally Invasive Thoracic Surgery Download
A Phase 1/2 study testing Olympus VE2 NIR Imaging System and Indocyanine green in people with Lung Neoplasms and Esophageal Lesion, run by Massachusetts General Hospital at 1 site in United States.
Trial summary
This will be a prospective, (NSR), single-center feasibility study of the Olympus VE2 NIR Imaging System to assess perfusion using NIR during minimally invasive esophagectomy and pulmonary segmentectomy. The aims of the study are: 1. To utilize NIR intraoperative imaging with the Olympus VE2 NIR Imaging System to: i. Read more about this study
- Who is it for?
- Any ageHealthy volunteers can take part
- Conditions the study is for
- Lung Neoplasms, Esophageal Lesion
- What is being tested?
- Olympus VE2 NIR Imaging System and Indocyanine green
- Type of treatment
- Injection or infusion, Medical device
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 38 participants
- Where
- 1 siteUnited States
- Study dates
- 29 Oct 2020to 3 Jun 2025
- Phase
- Phase 1/2
- 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 Any age
- All sexes
- Healthy volunteers accepted
- Child, Adult, Older adult
Who may be able to join
- -Subject has a suspicious lung lesion for which a minimally invasive segmentectomy is planned -OR- sub-ject has an esophageal lesion for which an esophagectomy is planned -
- Subject is 18 years of age or older
- Subject is willing and able to provide informed consent
Who cannot join
- Subject is not eligible for surgical resection as determined by the treating physician
- Subject has known or suspected allergy to Iodine, shellfish or intravenous contrast
- Subject is not eligible or considered high risk for surgical resection as determined by pre-operative spirometry
- Subject is female and of childbearing age who is currently pregnant or who is planning to become pregnant within the study
- Subject is unable and unwilling to provide informed consent
- Subject has liver disease or is taking drugs impact liver metabolism.
Trial locations and contacts
1 site in 1 country.
United States1 site
Massachusetts General Hospital
Boston, Massachusetts, 02114
About this study
Official title: Near-Infrared Perfusion During Minimally Invasive Thoracic Surgery
This will be a prospective, (NSR), single-center feasibility study of the Olympus VE2 NIR Imaging System to assess perfusion using NIR during minimally invasive esophagectomy and pulmonary segmentectomy. The aims of the study are:
- To utilize NIR intraoperative imaging with the Olympus VE2 NIR Imaging System to: i. Characterize gastric conduit perfusion during esophagectomy and, ii. Identify segmental anatomy during sublobar pulmonary resection (segmentectomy) after intraoperative, intravenous delivery of low-dose 0.15 mg/kg of ICG.
Read the detailed description
Current Surgical Approaches to Thoracic Malignancies are Imperfect: Thoracic malignancies are among the most deadly cancers diagnosed across the world. Non-small cell lung cancer (NSCLC) remains the number one cause of cancer related mortality in the United States and across the world. Esophageal cancer is the second most common thoracic malignancy, and is the fastest growing malignancy in the United States. Together, these 2 tumor types account for more an annual mortality of 150,000 in the United States alone. For patients with stage I and stage II disease, surgery provides the best opportunity for long-term survivorship for both malignancies; however, operative intervention is associated with significant morbidity and upwards of 20% of patients have complications.
As with surgery involving other body cavities, safe oncologic resection of thoracic tumors involves a careful understanding of the arterial blood flow to tissues that are to be (1) resected and (2) left behind. Despite the importance of these considerations, there remains very few tools to help the surgeon with this assessment. Two examples of these clinical dilemmas involve (1) pulmonary artery delineation during pulmonary segmentectomy and (2) conduit assessment during esophagectomy. Consequences of improper perfusion assessment can involve a variety of complications such as leak, stricture, abscess, or unnecessary resection.
This protocol describes a tool to address these unmet needs. More specificall, this non-significant risk study will assess feasibility of the Olympus VISERA ELITE II Near-infrared (VE2 NIR) Imaging System (Olympus Medical Systems Corp., Tokyo, Japan to intraoperatively assess perfusion during (1) pulmonary segmentectomy and (2) gastric conduit perfusion during esophagectomy by detecting systemically delivered indocyanine green (ICG). The VE2 NIR Imaging system has obtained 510k clearance from the US FDA for blood flow and related tissue perfusion.
Indocyanine Green (ICG): Indocyanine green is a water-soluble, NIR fluorophore with a molecular weight of 774.9 kDA. When intravenously delivered, ICG binds to plasma albumin thus creating a circulating nanoparticle. The main mechanism of excretion is hepatic as the liver excretes more than 80% of the available ICG in less than 24 hours. ICG is the most intensively studied NIR contrast agent and was approved by the United States Food and Drug Administration (FDA) for human administration in 1958. As a fluorophore, ICG has a peak absorption wavelength of 805 nm and a peak emission wavelength of 830 nm. ICG is inexpensive, non-toxic and readily available, making it an ideal contrast agent for intraoperative NIR imaging. The FDA specifically approves ICG for cardiac output, hepatic function and ophthalmic angiography.
Previous clinical data pertaining to ICG-based NIR imaging of gastric conduit perfusion at the time of esophagectomy: Esophagectomy remains a mainstay of multi-modality therapy for esophageal cancer. During esophagectomy, the diseased esophagus is resected and the remaining portion of the stomach (gastric conduit) is brought through the chest where it is anastomosed to either the thoracic or cervical esophagus. Anastomotic and conduit complications significantly contribute to morbidity and mortality associated with esophagectomy. Adequate vascular perfusion of the gastric conduit is vital to avoid these complications. To date, conduit viability is assessed intraoperatively by surgeon observational assessment, which is subjective. Thoracic surgeons are in desperate need of new technologies that can better assess tissue perfusion and ischemia of the gastric conduit. One such technique is the use of intraoperative NIR imaging with ICG to directly assess these parameters.
To date, hundreds of patients have been involved studies of NIR imaging with ICG to assess gastric conduit perfusion. In this approach, low dose ICG (2.5mg-25mg) is intravenously delivered and imaging of the neo-esophageal conduit commences 30 seconds later. In a review of over 420 patients undergoing this approach, this NIR signal was found to be reproducible, with no observed toxicity. Authors reported benefits of NIR imaging in identifying otherwise non-detectable transverse vessels between the terminal arcade and the short gastric arteries. Perhaps more convincing, in a propensity score matched study involving over 214 subjects, patients undergoing esophagectomy with the addition of NIR with ICG were found to have a 3-fold decrease (p=0.03) in anastomotic complications when compared to those undergoing traditional esophagectomy. Our goal is to utilize the Olympus VE2 NIR Imaging System with ICG to evaluate gastric conduit perfusion during minimally invasive esophagectomy.
Previous clinical experiences involving ICG-based NIR imaging to assess segmental anatomy during pulmonary resection: According to 2019 National Comprehensive Cancer Network (NCCN) Guidelines, the gold-standard treatment of resectable malignant pulmonary lesions requires anatomic resection (pneumonectomy, lobectomy or segmentectomy) with lymph node sampling. For patients with lesions larger than 2cm, lobectomy or pneumonectomy is typical. However, for lesions less than 2cm segmentectomy has been demonstrated to provide equivalent oncologic outcomes while also preserving functional lung parenchyma. Despite parenchymal sparing benefits, anatomic delineation of pulmonary segments is challenging and inaccurate. Current segmentectomy approaches involve careful clamping of those segmental airways supplying lung parenchyma involved with tumor burden, followed by insufflation of the ipsilateral lung. Using this approach, the non-clamped (cancer free) lung inflates while the clamped (lung to be resected) remains atelectatic. The surgeon then resects the "non-inflated" lung. Because of collateral ventilatory networks among alveoli and obstructive changes associated with lung cancer, lines of demarcation between these lung areas is often unclear. Inaccurate resection along segmental planes may result in retention of devascularized tissue, inadequate surgical margins, or incomplete clearing of draining lymphatic pathways.
Given challenges associated with current segmentectomy approaches, many groups have begun utilizing intraoperative NIR imaging with ICG to better demarcate segmental anatomy. To date, thousands of patients across dozens of institutions have utilized this method. In this approach, low dose ICG (ranging from 10-50mg) is delivered intravenously after clamping segmental pulmonary artery. Within minutes of ICG delivery, unclamped (healthy) parenchyma demonstrates a strong NIR signal which is detected using a modified thoracoscope, while the clamped (to be resected) tissue remains dark. In these studies reporting toxicity, there were minimal side effects from the ICG delivery. Our goal is to utilze the Olympus VE2 NIR Imaging System when used with ICG to assess segmental perfusion anatomy during minimally invasive sublobar pulmonary segmentectomy.
- Conditions
- Lung Neoplasms, Esophageal Lesion
- Being tested
- Olympus VE2 NIR Imaging System, Indocyanine green
- Medical subject headings
- Lung Neoplasms
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Olympus VE2 NIR Imaging SystemDevice
A prospective, (NSR), single-center feasibility study of the Olympus VE2 NIR Imaging System to assess perfusion using NIR during minimally invasive esophagectomy or pulmonary segmentectomy based on treatment arm.
Indocyanine greenDrug
intravenous delivery of low-dose 0.15 mg/kg of ICG combined with Olympus VE2 NIR Imaging System to assess perfusion using NIR during minimally invasive esophagectomy or pulmonary segmentectomy based on treatment arm
| Study group | Role | What they receive |
|---|---|---|
| During Minimally Invasive Pulmonary Segmentectomy (Group 2) | Experimental | Not described Receives: Device: Olympus VE2 NIR Imaging System; Drug: Indocyanine green |
| During Minimally Invasive Esophagectomy (Group 1) | Experimental | Not described Receives: Device: Olympus VE2 NIR Imaging System; Drug: Indocyanine green |
What is being measured
The primary outcome is the main question the study is designed to answer.
To utilize NIR intraoperative imaging with the Olympus VE2 NIR Imaging System for esophagectomy patients.
Fluorescent intensity, visualization of the intersegmental plane with NIR imaging, image quality will all be ranked by the surgeon as "below standard, average, or good" compared to the standard of care as they identify segmental anatomy during sublobar pulmonary resection (segmentectomy) after intraoperative, intravenous delivery of low-dose 0.15 mg/kg of ICG.
Measured: During surgery
To utilize NIR intraoperative imaging with the Olympus VE2 NIR Imaging System for segmentectomy patients.
Fluorescent intensity, visualization of the intersegmental plane with NIR imaging, image quality will all be ranked by the surgeon as "below standard, average, or good" compared to the standard of care as they identify esophageal anatomy during esophagectomy after intraoperative, intravenous delivery of low-dose 0.15 mg/kg of ICG.
Measured: During surgery
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted26 Apr 2022
- Study start29 Oct 2020
- Primary completion3 Jun 2025
- Study completion3 Jun 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (2)Papers the sponsor has linked to this study.
- Other trials for Lung NeoplasmsStudies of the same condition, open and under way.
- More trials run by Massachusetts General HospitalThe sponsor's other registered studies.
- 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 1/2
- Primary purpose
- Other
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Model description
- The treatment arms are separated by type of surgery. Arm 1 is esophagectomy, Arm 2 is segmentectomy.
- Masking
- None (open label)
- Enrolment
- 38 participants (actual)
Sponsor and investigators
- Lead sponsor
- Massachusetts General Hospital
- Sponsor type
- University, hospital or other
- Collaborators
- Olympus
- Responsible party
- Principal investigator, Christopher R. Morse, M.D., Massachusetts General Hospital
- Investigators
- Christopher Morse, MD, Principal investigator, Massachusetts General Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05346380
- Sponsor's protocol ID
- 2020P000835
- Status last verified
- Nov 2025
- First submitted
- 11 Feb 2022
- Last updated
- 26 Nov 2025
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
- Individual data sharing
- Undecided: Sharing device and surgical data with Olympus, however no PHI will be shared.
Publications
DeLong JC, Kelly KJ, Jacobsen GR, Sandler BJ, Horgan S, Bouvet M. The benefits and limitations of robotic assisted transhiatal esophagectomy for esophageal cancer. J Vis Surg. 2016 Sep 8;2:156. doi: 10.21037/jovs.2016.09.01. eCollection 2016.
PubMed 29078542Siegel RL, Miller KD, Jemal A. Cancer statistics, 2019. CA Cancer J Clin. 2019 Jan;69(1):7-34. doi: 10.3322/caac.21551. Epub 2019 Jan 8.
PubMed 30620402
Study at a glance
From the registry record, last updated by the sponsor on 26 Nov 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Near-Infrared Perfusion During Minimally Invasive Thoracic Surgery
- ClinicalTrials.gov ID
- NCT05346380
- Acronym / sponsor ID
- 2020P000835
- Conditions
- Lung Neoplasms, Esophageal Lesion
- Phase
- Phase 1/2
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 38 participants (actual)
- Lead sponsor
- Massachusetts General HospitalUniversity, hospital or other
- Collaborators
- Olympus
- Study start
- 29 Oct 2020 (actual)
- Primary completion
- 3 Jun 2025 (actual)
- Study completion
- 3 Jun 2025 (actual)
- First posted
- 26 Apr 2022 (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.
This will be a prospective, (NSR), single-center feasibility study of the Olympus VE2 NIR Imaging System to assess perfusion using NIR during minimally invasive esophagectomy and pulmonary segmentectomy. The aims of the study are:
- To utilize NIR intraoperative imaging with the Olympus VE2 NIR Imaging System to: i. Characterize gastric conduit perfusion during esophagectomy and, ii. Identify segmental anatomy during sublobar pulmonary resection (segmentectomy) after intraoperative, intravenous delivery of low-dose 0.15 mg/kg of ICG.
Detailed description
Current Surgical Approaches to Thoracic Malignancies are Imperfect: Thoracic malignancies are among the most deadly cancers diagnosed across the world. Non-small cell lung cancer (NSCLC) remains the number one cause of cancer related mortality in the United States and across the world. Esophageal cancer is the second most common thoracic malignancy, and is the fastest growing malignancy in the United States. Together, these 2 tumor types account for more an annual mortality of 150,000 in the United States alone. For patients with stage I and stage II disease, surgery provides the best opportunity for long-term survivorship for both malignancies; however, operative intervention is associated with significant morbidity and upwards of 20% of patients have complications.
As with surgery involving other body cavities, safe oncologic resection of thoracic tumors involves a careful understanding of the arterial blood flow to tissues that are to be (1) resected and (2) left behind. Despite the importance of these considerations, there remains very few tools to help the surgeon with this assessment. Two examples of these clinical dilemmas involve (1) pulmonary artery delineation during pulmonary segmentectomy and (2) conduit assessment during esophagectomy. Consequences of improper perfusion assessment can involve a variety of complications such as leak, stricture, abscess, or unnecessary resection.
This protocol describes a tool to address these unmet needs. More specificall, this non-significant risk study will assess feasibility of the Olympus VISERA ELITE II Near-infrared (VE2 NIR) Imaging System (Olympus Medical Systems Corp., Tokyo, Japan to intraoperatively assess perfusion during (1) pulmonary segmentectomy and (2) gastric conduit perfusion during esophagectomy by detecting systemically delivered indocyanine green (ICG). The VE2 NIR Imaging system has obtained 510k clearance from the US FDA for blood flow and related tissue perfusion.
Indocyanine Green (ICG): Indocyanine green is a water-soluble, NIR fluorophore with a molecular weight of 774.9 kDA. When intravenously delivered, ICG binds to plasma albumin thus creating a circulating nanoparticle. The main mechanism of excretion is hepatic as the liver excretes more than 80% of the available ICG in less than 24 hours. ICG is the most intensively studied NIR contrast agent and was approved by the United States Food and Drug Administration (FDA) for human administration in 1958. As a fluorophore, ICG has a peak absorption wavelength of 805 nm and a peak emission wavelength of 830 nm. ICG is inexpensive, non-toxic and readily available, making it an ideal contrast agent for intraoperative NIR imaging. The FDA specifically approves ICG for cardiac output, hepatic function and ophthalmic angiography.
Previous clinical data pertaining to ICG-based NIR imaging of gastric conduit perfusion at the time of esophagectomy: Esophagectomy remains a mainstay of multi-modality therapy for esophageal cancer. During esophagectomy, the diseased esophagus is resected and the remaining portion of the stomach (gastric conduit) is brought through the chest where it is anastomosed to either the thoracic or cervical esophagus. Anastomotic and conduit complications significantly contribute to morbidity and mortality associated with esophagectomy. Adequate vascular perfusion of the gastric conduit is vital to avoid these complications. To date, conduit viability is assessed intraoperatively by surgeon observational assessment, which is subjective. Thoracic surgeons are in desperate need of new technologies that can better assess tissue perfusion and ischemia of the gastric conduit. One such technique is the use of intraoperative NIR imaging with ICG to directly assess these parameters.
To date, hundreds of patients have been involved studies of NIR imaging with ICG to assess gastric conduit perfusion. In this approach, low dose ICG (2.5mg-25mg) is intravenously delivered and imaging of the neo-esophageal conduit commences 30 seconds later. In a review of over 420 patients undergoing this approach, this NIR signal was found to be reproducible, with no observed toxicity. Authors reported benefits of NIR imaging in identifying otherwise non-detectable transverse vessels between the terminal arcade and the short gastric arteries. Perhaps more convincing, in a propensity score matched study involving over 214 subjects, patients undergoing esophagectomy with the addition of NIR with ICG were found to have a 3-fold decrease (p=0.03) in anastomotic complications when compared to those undergoing traditional esophagectomy. Our goal is to utilize the Olympus VE2 NIR Imaging System with ICG to evaluate gastric conduit perfusion during minimally invasive esophagectomy.
Previous clinical experiences involving ICG-based NIR imaging to assess segmental anatomy during pulmonary resection: According to 2019 National Comprehensive Cancer Network (NCCN) Guidelines, the gold-standard treatment of resectable malignant pulmonary lesions requires anatomic resection (pneumonectomy, lobectomy or segmentectomy) with lymph node sampling. For patients with lesions larger than 2cm, lobectomy or pneumonectomy is typical. However, for lesions less than 2cm segmentectomy has been demonstrated to provide equivalent oncologic outcomes while also preserving functional lung parenchyma. Despite parenchymal sparing benefits, anatomic delineation of pulmonary segments is challenging and inaccurate. Current segmentectomy approaches involve careful clamping of those segmental airways supplying lung parenchyma involved with tumor burden, followed by insufflation of the ipsilateral lung. Using this approach, the non-clamped (cancer free) lung inflates while the clamped (lung to be resected) remains atelectatic. The surgeon then resects the "non-inflated" lung. Because of collateral ventilatory networks among alveoli and obstructive changes associated with lung cancer, lines of demarcation between these lung areas is often unclear. Inaccurate resection along segmental planes may result in retention of devascularized tissue, inadequate surgical margins, or incomplete clearing of draining lymphatic pathways.
Given challenges associated with current segmentectomy approaches, many groups have begun utilizing intraoperative NIR imaging with ICG to better demarcate segmental anatomy. To date, thousands of patients across dozens of institutions have utilized this method. In this approach, low dose ICG (ranging from 10-50mg) is delivered intravenously after clamping segmental pulmonary artery. Within minutes of ICG delivery, unclamped (healthy) parenchyma demonstrates a strong NIR signal which is detected using a modified thoracoscope, while the clamped (to be resected) tissue remains dark. In these studies reporting toxicity, there were minimal side effects from the ICG delivery. Our goal is to utilze the Olympus VE2 NIR Imaging System when used with ICG to assess segmental perfusion anatomy during minimally invasive sublobar pulmonary segmentectomy.
Study design
- Primary purpose
- Other
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
- Model description
- The treatment arms are separated by type of surgery. Arm 1 is esophagectomy, Arm 2 is segmentectomy.
| Arm | Type | Receives |
|---|---|---|
| During Minimally Invasive Pulmonary Segmentectomy (Group 2) | Experimental | Device: Olympus VE2 NIR Imaging System, Drug: Indocyanine green |
| During Minimally Invasive Esophagectomy (Group 1) | Experimental | Device: Olympus VE2 NIR Imaging System, Drug: Indocyanine green |
Who may qualify
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (3 listed)
- -Subject has a suspicious lung lesion for which a minimally invasive segmentectomy is planned -OR- sub-ject has an esophageal lesion for which an esophagectomy is planned -
- Subject is 18 years of age or older
- Subject is willing and able to provide informed consent
Key exclusion criteria (6 listed)
- Subject is not eligible for surgical resection as determined by the treating physician
- Subject has known or suspected allergy to Iodine, shellfish or intravenous contrast
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 |
|---|---|---|
| Olympus VE2 NIR Imaging SystemA prospective, (NSR), single-center feasibility study of the Olympus VE2 NIR Imaging System to assess perfusion using NIR during minimally invasive esophagectomy or pulmonary segmentectomy based on treatment arm. | Device | During Minimally Invasive Esophagectomy (Group 1), During Minimally Invasive Pulmonary Segmentectomy (Group 2) |
| Indocyanine greenintravenous delivery of low-dose 0.15 mg/kg of ICG combined with Olympus VE2 NIR Imaging System to assess perfusion using NIR during minimally invasive esophagectomy or pulmonary segmentectomy based on treatment arm | Drug | During Minimally Invasive Esophagectomy (Group 1), During Minimally Invasive Pulmonary Segmentectomy (Group 2) |
Primary outcome
To utilize NIR intraoperative imaging with the Olympus VE2 NIR Imaging System for esophagectomy patients.
Time frame: During surgery
Fluorescent intensity, visualization of the intersegmental plane with NIR imaging, image quality will all be ranked by the surgeon as "below standard, average, or good" compared to the standard of care as they identify segmental anatomy during sublobar pulmonary resection (segmentectomy) after intraoperative, intravenous delivery of low-dose 0.15 mg/kg of ICG.
To utilize NIR intraoperative imaging with the Olympus VE2 NIR Imaging System for segmentectomy patients.
Time frame: During surgery
Fluorescent intensity, visualization of the intersegmental plane with NIR imaging, image quality will all be ranked by the surgeon as "below standard, average, or good" compared to the standard of care as they identify esophageal anatomy during esophagectomy after intraoperative, intravenous delivery of low-dose 0.15 mg/kg of ICG.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 26 Nov 2025.
- Background: PubMed 29078542DeLong JC, Kelly KJ, Jacobsen GR, Sandler BJ, Horgan S, Bouvet M. The benefits and limitations of robotic assisted transhiatal esophagectomy for esophageal cancer. J Vis Surg. 2016 Sep 8;2:156. doi: 10.21037/jovs.2016.09.01. eCollection 2016.
- Background: PubMed 30620402Siegel RL, Miller KD, Jemal A. Cancer statistics, 2019. CA Cancer J Clin. 2019 Jan;69(1):7-34. doi: 10.3322/caac.21551. Epub 2019 Jan 8.
- Individual participant dataSharing planned: Undecided. Sharing device and surgical data with Olympus, however no PHI will be shared.
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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.
Christopher Morse, MD principal investigator
Massachusetts General Hospital
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 1/2 study testing Olympus VE2 NIR Imaging System and Indocyanine green in people with Lung Neoplasms and Esophageal Lesion, run by Massachusetts General Hospital 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 3 inclusion and 6 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: finished, as of the sponsor's last update on 26 Nov 2025. 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.
What does this combined phase mean?
Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
To utilize NIR intraoperative imaging with the Olympus VE2 NIR Imaging System for esophagectomy patients. (time frame: During surgery). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT05346380, which also lists 2 linked publications.
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 26 Nov 2025.