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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06254833
Other study ID # 311249-00001
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 1, 2023
Est. completion date November 1, 2024

Study information

Verified date February 2024
Source University of California, San Diego
Contact Shanglei Liu
Phone (858)249-1837
Email jtt005@health.ucsd.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

using microdosing of ICG vs regular dosing of ICG for perfusion assessment during surgery


Description:

Randomized dosing of 7.5mg or 0.75mg of ICG injection during surgery for bowel perfusion assessment using new imaging equipment


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date November 1, 2024
Est. primary completion date October 1, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - all patient undergoing intestinal resection surgery Exclusion Criteria: - pregnancy, renal insufficiency

Study Design


Related Conditions & MeSH terms


Intervention

Other:
micro dosing of ICG
smaller dose of injection of ICG. All devices used are FDA approved in clinical use.

Locations

Country Name City State
United States UC San Diego La Jolla California

Sponsors (1)

Lead Sponsor Collaborator
Shanglei Liu

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary ability to assess perfusion likert scale evaluation survey performed by surgeon up to 30 days post operatively
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