ImagingJURANCT07259759
JURA Study - Observational First-in-human Feasibility Study
An observational study of Imaging, run by Intuitive Surgical at 1 site in Netherlands.
Trial summary
Evaluate the functionality of the JURA System v. 1.0 Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Imaging
- What is being tested?
- Visualization / Imaging
- Type of treatment
- Medical device
- How many people
- 20 participants
- Where
- 1 siteNetherlands
- Study dates
- 31 Oct 2025to 27 Mar 2026
- Phase
- Observational
- 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
- No healthy volunteers
- Adult, Older adult
Study population: Men and women above the age of 18 year, scheduled for an elective abdominal minimal invasive surgery
Who may be able to join
- Men and women ≥ 18 years of age
- Patient scheduled for an elective abdominal minimal invasive surgery
Who cannot join
- Pregnancy, or positive pregnancy test for women prior to menopause or breastfeeding women
- Individuals who are unable to fully understand all aspects of the study as relevant to the decision to participate (mentally or verbally), or who could be manipulated or unduly influenced due to of a compromised position, expectation or benefits or fear or retaliation
Trial locations and contacts
1 site in 1 country.
About this study
Evaluate the functionality of the JURA System v. 1.0
Read the detailed description
Evaluate the functionality of the JURA System v. 1.0 in humans under real clinical conditions in the operating room
- Conditions
- Imaging
- Being tested
- Visualization / Imaging
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Visualization / ImagingDevice
Visualization / Imaging of organs, structures and tissue of interest using the JURA system such as for example spleen, anastomosis of colon, omental fat, pancreas
| Study group | Role | What they receive |
|---|---|---|
| JURA Group | Visualization of organs, structures and tissue of interest using the JURA System during a surgical procedure. The surgical procedure itself will be conducted exclusively following the site standard of care. Receives: Device: Visualization / Imaging |
What is being measured
The primary outcome is the main question the study is designed to answer.
Image quality of the JURA System v. 1.0 in humans
Image quality of the JURA System v. 1.0 in humans using an image quality assessment score
Measured: Intra-Operative
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted2 Dec 2025
- Study start31 Oct 2025
- Primary completion27 Mar 2026
- Study completion27 Mar 2026
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for ImagingStudies of the same condition, open and under way.
- More trials run by Intuitive SurgicalThe 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
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 20 participants (actual)
Sponsor and investigators
- Lead sponsor
- Intuitive Surgical
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07259759
- Sponsor's protocol ID
- 1145917C
- Acronym
- JURA
- Status last verified
- Apr 2026
- First submitted
- 25 Sep 2025
- Last updated
- 29 Apr 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 29 Apr 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- JURA Study - Observational First-in-human Feasibility Study
- ClinicalTrials.gov ID
- NCT07259759
- Acronym / sponsor ID
- JURA / 1145917C
- Conditions
- Imaging
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 20 participants (actual)
- Lead sponsor
- Intuitive SurgicalIndustry (pharma, biotech, devices)
- Study start
- 31 Oct 2025 (actual)
- Primary completion
- 27 Mar 2026 (actual)
- Study completion
- 27 Mar 2026 (actual)
- First posted
- 2 Dec 2025 (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.
Evaluate the functionality of the JURA System v. 1.0
Detailed description
Evaluate the functionality of the JURA System v. 1.0 in humans under real clinical conditions in the operating room
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| JURA Group | – | Device: Visualization / ImagingVisualization of organs, structures and tissue of interest using the JURA System during a surgical procedure. The surgical procedure itself will be conducted exclusively following the site standard of care. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Men and women above the age of 18 year, scheduled for an elective abdominal minimal invasive surgery
Key inclusion criteria (2 listed)
- Men and women ≥ 18 years of age
- Patient scheduled for an elective abdominal minimal invasive surgery
Key exclusion criteria (2 listed)
- Pregnancy, or positive pregnancy test for women prior to menopause or breastfeeding women
- Individuals who are unable to fully understand all aspects of the study as relevant to the decision to participate (mentally or verbally), or who could be manipulated or unduly influenced due to of a compromised position, expectation or benefits or fear or retaliation
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 |
|---|---|---|
| Visualization / ImagingVisualization / Imaging of organs, structures and tissue of interest using the JURA system such as for example spleen, anastomosis of colon, omental fat, pancreas | Device | JURA Group |
Primary outcome
Image quality of the JURA System v. 1.0 in humans
Time frame: Intra-Operative
Image quality of the JURA System v. 1.0 in humans using an image quality assessment score
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 29 Apr 2026.
- 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.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Imaging, run by Intuitive Surgical at 1 site in Netherlands.
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 2 inclusion and 2 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 29 Apr 2026. 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 Netherlands. 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?
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?
Image quality of the JURA System v. 1.0 in humans (time frame: Intra-Operative). 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 29 Apr 2026.