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CompletedNCT00285506Updated May 29, 2006

The Effect of Contrast Media on Erythrocytes in Healthy Volunteers

An observational study in Healthy Volunteers, sponsored by Medical University of South Carolina. Completed at 1 site in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2006-05-29.

Sponsored by Medical University of South Carolina · Observational

Study type
Observational
Time perspective
Other
Enrollment
20
Ages
18 Years and older
Sex
All
01

Study summary

The purpose of the study is to test the effect that contrast media (dye) has on cellular integrity (structure)

Read the detailed description

The influence of several radiological contrast media on erythrocyte morphology and function has been investigated in the past (1). However, published data is sparse and does not include the assessment of iso-osmolar agents as compared to low-osmolar agents.

In addition, the effect of the injection of contrast media at higher temperatures (i.e. > room or body temperature), which may be beneficial for the rapid injection of more viscous contrast media at multi detector-row CT angiography, has never been evaluated.

We intend to assess the hypothesis, that iso-osmolar contrast media (i.e. Visipaque) exerts less effect on erythrocyte morphology and function as compared to low-osmolar agents.

In addition, we intend to identify the upper temperature limit, at which contrast media can be injected, without affecting erythrocyte integrity.

Subjects will have up tp 400 mLs (approximately 26 tablespoons) of blood drawn. The blood will be kept at body temperature in a petri dish or similar container and exposed to contrast media (dye).

02

Conditions studied

  • Healthy Volunteers

Keywords

  • Healthy Volunteers
03

In context

Lead sponsor

Medical University of South Carolina is the lead sponsor of 852 studies on the registry; 165 are open to participants now.

Of its 128 completed or terminated interventional studies of FDA-regulated products, 101 (79%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Subjects must be at least 18 years old
  • Subjects must be at least 110lbs and

Exclusion criteria

Exclusion Criteria:

  • Subjects may not be pregnant
  • Subjects must not possess any medical conditions that would preclude them from participating
05

Study design

Time perspective
Other
Enrollment
20 participants
06

Study locations

1 site
  • Medical University of South Carolina
    Charleston, South Carolina 29425, United States
07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 29, 2006, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT00285506
Lead sponsor
Medical University of South Carolina
Collaborators
GE Healthcare
First posted
Feb 2, 2006
Start date
Jan 2006
Completion
Jan 2006
Last update
May 29, 2006

Study contacts

U. Joseph Schoepf, MD
principal investigator · Medical University of South Carolina
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2006. You cannot join it, but the record below documents what was studied.

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