Trials / Completed
CompletedNCT04200417
Chemoembolization for Lung Tumors
Phase I Study of Transarterial Chemoembolization of Lung Metastases
- Status
- Completed
- Phase
- Phase 1
- Study type
- Interventional
- Enrollment
- 10 (actual)
- Sponsor
- Memorial Sloan Kettering Cancer Center · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This study is being done to determine if it is safe to perform lung chemoembolization and if the lung chemoembolization procedure can successfully deliver chemotherapy to lung tumors.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Chemoembolization | Chemoembolization will be performed via the artery (bronchial, non-bronchial systemic, or pulmonary) that shows the greatest tumor enhancement on angiography. Chemoembolization will be performed using a lipiodol / mitomycin emulsion, followed by spherical particles. |
| DRUG | Mitomycin C | Mitomycin (5mg/m\^2,maximum mitomycin dose 20 mg) will be dissolved in lipiodol at 2 mg/ml on the day of procedure. |
| DRUG | Lipiodol | Mitomycin (5mg/m\^2,maximum mitomycin dose 20 mg) will be dissolved in lipiodol at 2 mg/ml on the day of procedure. |
| DRUG | Embospheres | Embospheres are non-resorbable spherical microspheres (trisacryl gelatin) that are FDA-approved for embolization of hypervascular tumors. |
Timeline
- Start date
- 2019-12-13
- Primary completion
- 2022-04-19
- Completion
- 2022-04-19
- First posted
- 2019-12-16
- Last updated
- 2025-05-16
Locations
4 sites across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT04200417. Inclusion in this directory is not an endorsement.