Robotic Adrenalectomy With Versus Without Indocyanine Green Fluorescence Imaging
Randomized Prospective Study of Robotic Adrenalectomy With Versus Without Indocyanine Green Fluorescence Imaging
1 other identifier
interventional
55
1 country
1
Brief Summary
This is a prospective randomized study comparing robotic adrenalectomy with versus without intraoperative indocyanine green imaging.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jul 2026
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 31, 2026
CompletedFirst Submitted
Initial submission to the registry
September 4, 2026
CompletedFirst Posted
Study publicly available on registry
September 10, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 30, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 31, 2027
September 10, 2026
September 1, 2026
1.4 years
September 4, 2026
September 4, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
dissection time
duration of time for adrenal dissection in robotic adrenalectomy
intraoperative
Study Arms (2)
adrenalectomy with indocyanine green imaging
ACTIVE COMPARATORrobotic adrenalectomy with intraoperative indocyanine green imaging
conventional adrenalectomy
NO INTERVENTIONconventional robotic adrenalectomy without intraoperative indocyanine green imaging
Interventions
intraoperative use of indocyanine green imaging during robotic adrenalectomy
Eligibility Criteria
You may qualify if:
- adult patients scheduled for robotic adrenalectomy
You may not qualify if:
- patients scheduled for laparoscopic or open adrenalectomy or with an iodine allergy
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Cleveland Clinic Foundation
Cleveland, Ohio, 44195, United States
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Study Coordinator
Study Record Dates
First Submitted
September 4, 2026
First Posted
September 10, 2026
Study Start
July 31, 2026
Primary Completion (Estimated)
December 30, 2027
Study Completion (Estimated)
December 31, 2027
Last Updated
September 10, 2026
Record last verified: 2026-09