NCT07813247

Brief Summary

This is a prospective randomized study comparing robotic adrenalectomy with versus without intraoperative indocyanine green imaging.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
55

participants targeted

Target at P25-P50 for not_applicable

Timeline
15mo left

Started Jul 2026

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress13%
Jul 2026Dec 2027

Study Start

First participant enrolled

July 31, 2026

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

September 4, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

September 10, 2026

Completed
1.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 30, 2027

Expected
1 day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2027

Last Updated

September 10, 2026

Status Verified

September 1, 2026

Enrollment Period

1.4 years

First QC Date

September 4, 2026

Last Update Submit

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 COMPARATOR

robotic adrenalectomy with intraoperative indocyanine green imaging

Procedure: indocyanine green imaging

conventional adrenalectomy

NO INTERVENTION

conventional robotic adrenalectomy without intraoperative indocyanine green imaging

Interventions

intraoperative use of indocyanine green imaging during robotic adrenalectomy

adrenalectomy with indocyanine green imaging

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

RECRUITING

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

Locations