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NCT03097627

Intravenous Indocyanine Green for Localization of Intra-thoracic Lesions

Completed Phase 1, PHASE2 Last updated 12 December 2017
What this trial tests

Phase 1, PHASE2 trial testing ICG Intervention in Pulmonary Nodule, Solitary in 4 participants. Completed in 28 October 2016.

Timeline
1 February 2016
Primary endpoint
28 October 2016
28 October 2016

Quick facts

Lead sponsorBrigham and Women's Hospital
PhasePhase 1, PHASE2
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposedevice feasibility
Enrollment4
Start date1 February 2016
Primary completion28 October 2016
Estimated completion28 October 2016
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Brigham and Women's Hospital

Who can join

18 and older, any sex, with Pulmonary Nodule, Solitary or Pulmonary Nodule, Multiple. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a clinical trial to evaluate the intravenous administration of indocyanine green (ICG) as a method of intra-thoracic lesion localization. The primary purpose is to determine if intravenous ICG allows us to identify intra-thoracic lesions.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of ICG Intervention

Trials testing the same drug.

Other recruiting trials for Pulmonary Nodule, Solitary

Currently open trials in the same condition.

Other Brigham and Women's Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03097627.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing