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NCT02753881 · ClinicalTrials.gov registry record · Phase 1

Pharmacokinetics of Doxorubicin in cTACE of Liver Cancer

A Phase 1 study of Liver Cancer, sponsored by Yale University.

Completed
Registry status
Phase 1
Development phase
30
Enrollment target
1
Study location

NCT02753881 is a Phase 1 study of Liver Cancer that has completed, run by Yale University. The registered enrollment target is 30 participants, below the 448-participant average among 78 other Liver Cancer trials with a reported enrollment target (93% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT02753881, a Phase 1 study of Liver Cancer, has completed, sponsored by Yale University.

COMPLETED
Registry status
Phase 1
Development phase
30 participants
Enrollment target
1
Study location

Study Summary

Patients with primary and secondary liver cancer may participate in this study. The purpose is to perform an analysis of the effects of doxorubicin and its metabolite doxorubicinol on the body (doxorubicin pharmacokinetics ) after conventional transarterial chemoembolization (cTACE). cTACE is a procedure in which chemotherapy drugs are injected, followed by an injection of small beads to block the tumor-feeding arteries. Doxorubicin is a chemotherapeutic agent used in the cTACE procedure. This study will examine doxorubicin pharmacokinetics in patients who: 1) receive whole liver cTACE; and 2) receive super-selective CTACE (i.e., delivered in close proximity to the tumor).

Conditions Studied

Interventions

  • DRUG whole liver lobe cTACE doxorubicin
  • DRUG superselective cTACE doxorubicin

Study Locations (1)

Connecticut

  • Yale University, Department of Diagnostic Radiology - New Haven

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2015-11
Est. Completion 2019-12
Phase Phase 1

Sponsor

Yale University

1,492 total trials

What the Registry Record Tells You About NCT02753881

The ClinicalTrials.gov registry entry for NCT02753881 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 448-participant average among 78 other Liver Cancer trials with a reported enrollment target (93% lower). The listed sponsor is Yale University, which has 1,492 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Liver Cancer appearing as the primary indexed condition, and to 2 interventions - of which whole liver lobe cTACE doxorubicin is the first listed.

NCT02753881 reports 1 study location spanning 1 distinct geographic area - top geographies include Connecticut.

Frequently Asked Questions

What is clinical trial NCT02753881 about?

NCT02753881 is a clinical study titled "Pharmacokinetics of Doxorubicin in cTACE of Liver Cancer". Patients with primary and secondary liver cancer may participate in this study. The purpose is to perform an analysis of the effects of doxorubicin and its metabolite doxorubicinol on the body (doxorubicin pharmacokinetics ) after conventional transarterial chemoembolization (cTACE). cTACE is a proc...

What is the current status of trial NCT02753881?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 30 participants. The study started on 2015-11. Estimated completion is 2019-12.

What conditions does trial NCT02753881 study?

This clinical trial studies the following conditions: Liver Cancer.

What interventions are being tested in trial NCT02753881?

The interventions under investigation include: whole liver lobe cTACE doxorubicin (DRUG), superselective cTACE doxorubicin (DRUG).

Who is sponsoring clinical trial NCT02753881?

This trial is sponsored by Yale University, which has 1,492 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02753881 being conducted?

This trial has 1 study location across Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.