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ow volume contrast dye for CT chest and abdomen angiography

Phase 1
Conditions
Health Condition 1: I00-I99- Diseases of the circulatory system
Registration Number
CTRI/2019/07/020192
Lead Sponsor
A
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Patients referred for CT Aortic Angiography with age from 30-80 years

Exclusion Criteria

Patients with endovascular stenting, unco-operative patients

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
CTDI vol (mGy) <br/ ><br>DLP- Dose Length Product (mGy.cm) <br/ ><br>Effective dose (mSv)Timepoint: CTDI vol (mGy)will be noted - 6 months <br/ ><br>DLP- Dose Length Product - 6 months (mGy.cm) <br/ ><br>Effective dose (mSv)
Secondary Outcome Measures
NameTimeMethod
Subjective and Objective image quality <br/ ><br>Assessment <br/ ><br>Timepoint: Subjective and Objective image quality <br/ ><br>Assessment - weekly one time
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