MedTrace Logo

Single-center Randomized Trial for Comparison of Performance Between Domestic and Imported Chemoport

NCT01733342 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 176

Last updated 2013-12-04

No results posted yet for this study

Summary

To compare the performance of domestic chemoport and imported chemoport

Conditions

Interventions

DEVICE

Celsite chemoport implantation

Celsite chemoport implantation was done under local anesthesia, at anterior chest wall, under ultrasound guidance

PROCEDURE

local anesthesia

chemoport implantation will be done under local anesthesia using lidocaine.

DEVICE

Humanport chemoport implantation

Humanport chemoport implantation was done under local anesthesia, at anterior chest wall, under ultrasound guidance

Sponsors & Collaborators

  • Seoul National University Hospital

    lead OTHER

Principal Investigators

  • Hyo-Cheol Kim, MD · Seoul National University Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-11-30
Primary Completion
2013-12-31
Completion
2013-12-31

Countries

  • South Korea

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01733342 on ClinicalTrials.gov