Skip to content

Comparison of contrast media Dixopaque (Shahid Ghazi) and Visipaque

Double-blinde, randomized clinical trial on efficacy and safety of Dixopaque (Shahid Ghazi) contrast media and Visipaque in coronary angiography

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201607254920N8
Enrollment
50
Registered
2016-12-25
Start date
2017-01-01
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients candidated for coronary angiography by contrast media. Ischemic Heart Diseases

Interventions

Intervention 1: Intervention: patients in this group based on randomization will receive Dixopaque of Shahid Ghazi with a single dose of 320 mg intravenously. Intervention 2: Control:patients in this
Diagnosis
Intervention: patients in this group based on randomization will receive Dixopaque of Shahid Ghazi with a single dose of 320 mg intravenously.
Control:patients in this group based of randomization will receive Visipaque with a single dose of 320 mg intravenously.

Sponsors

Shahid Ghazi Pharmaceutical Company
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: patients aged between 45 to 65 years old; referred subjects for coronary angiography by contrast media; provided signed and dated informed consent subjects. Exclusion criteria: patients with contrast administration in the past 7 days; subjects have known contra-indication and allergy to contrast administration; renal insufficiency as defined by GFR < 50; lactation; pregnancy; bronchial asthma; clinical unstable condition (hemodynamic, respiratory, neurologic); emergency cases; hyperthyroidism; end-stage patients.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Image Quality. Timepoint: After coronary angiograghy. Method of measurement: Scoring by investigator from 1 to 10.

Secondary

MeasureTime frame
Adverse events of contrast media. Timepoint: During injection and 24 after injection. Method of measurement: Interview, Physical exam, Lab test.;Renal toxicity. Timepoint: Before and 24 hours after injection. Method of measurement: Serum creatinine examination.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Ramin Heshmat

Chronic Diseases Research Center

rheshmat@tums.ac.ir+98 21 8835 4309

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026