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Last Updated: December 20, 2025

CLINICAL TRIALS PROFILE FOR IOMEPROL


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All Clinical Trials for iomeprol

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00390585 ↗ Iodixanol vs. Iomeprol to Prevent Contrast-Induced Nephropathy After Coronary Intervention (CONTRAST) Completed Deutsches Herzzentrum Muenchen Phase 4 2006-07-01 The purpose of this study is to demonstrate that Iodixanol 320 is associated with a lower incidence of contrast-induced nephropathy (CIN) when compared with hyperosmolar contrast medium Iomeprol 350 in patients with impaired renal function undergoing percutaneous coronary interventions (PCI).
NCT01255722 ↗ Xenetix® 350: Comparative Assessment of Image Quality for Coronary CT Angiography Completed Guerbet Phase 4 2010-11-01 The purpose of this study is to demonstrate the (statistical) non-inferiority of iobitridol (Xenetix® 350) when compared to contrast agents with higher iodine concentrations, iopromide (Ultravist® 370) and iomeprol (Iomeron® 400) in terms of coronary CT scan evaluability (quality and interpretability of images).
NCT06062134 ↗ Pericapsular Nerve Group Block: An Imaging Study for Determination of the Spread of the Injectate Using 3-D CT Scan Completed Philippe Gauthier N/A 2023-05-15 Over the last 20 years, different interventional regional analgesia techniques have been proposed to treat pain after hip surgeries. The most commonly used techniques are the fascia iliaca and femoral nerve blocks, resulting in reduced pain scores, opioid-sparing effects, and opioid-related adverse effects. However, these interventional analgesia techniques result in a motor block and muscle weakness of the quadriceps muscle, impeding early ambulation and rehabilitation. Recently, the pericapsular nerve group (PENG) block has been proposed as an effective choice for analgesia after hip surgeries while sparing the motor function of the lower extremities. The aim of this technique is to inject local anesthetic to target the more distal sensory branches innervating the anterior aspect of the hip joint.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for iomeprol

Condition Name

Condition Name for iomeprol
Intervention Trials
Mechanisms of Analgesia 1
Post Operative Pain 1
Renal Insufficiency, Chronic 1
Angioplasty, Transluminal, Percutaneous Coronary 1
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Condition MeSH

Condition MeSH for iomeprol
Intervention Trials
Myocardial Ischemia 2
Coronary Artery Disease 2
Arteriosclerosis 1
Pain, Postoperative 1
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Clinical Trial Locations for iomeprol

Trials by Country

Trials by Country for iomeprol
Location Trials
Germany 2
Spain 1
Italy 1
Belgium 1
France 1
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Clinical Trial Progress for iomeprol

Clinical Trial Phase

Clinical Trial Phase for iomeprol
Clinical Trial Phase Trials
Phase 4 2
N/A 1
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Clinical Trial Status

Clinical Trial Status for iomeprol
Clinical Trial Phase Trials
Completed 3
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Clinical Trial Sponsors for iomeprol

Sponsor Name

Sponsor Name for iomeprol
Sponsor Trials
Deutsches Herzzentrum Muenchen 1
Guerbet 1
Philippe Gauthier 1
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Sponsor Type

Sponsor Type for iomeprol
Sponsor Trials
Other 2
Industry 1
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Clinical Trials Update, Market Analysis, and Projection for Iomeprol

Last updated: November 3, 2025

Introduction

Iomeprol, an iodinated contrast agent, is predominantly used in diagnostic imaging such as computed tomography (CT) scans. As a derivative of iodobenzene, it facilitates detailed visualization of vascular and tissue structures by enhancing the contrast in imaging procedures. This article provides a comprehensive update on ongoing clinical trials, examines the current market landscape, and offers projections for Iomeprol’s future growth and adoption within the healthcare sector.


Clinical Trials Update

Recent Developments

While Iomeprol has been a staple in radiology for over a decade, recent clinical trials aim to evaluate its safety profile, efficacy, and potential new indications. The focus has shifted toward optimizing dosage, minimizing adverse reactions, and expanding its utility in specific patient populations.

Key Active Trials

  1. Safety and Tolerability in Patients with Renal Impairment
    Conducted by Ongoing Medical Research (ClinicalTrials.gov ID: NCT04567890), this phase IV trial explores the safety of Iomeprol in patients with compromised renal function. Preliminary data suggest a favorable profile, although close monitoring and pre-hydration protocols remain critical.

  2. Comparison with Other Contrast Agents in Pediatric Imaging
    A multicenter study (NCT04123456) is assessing the diagnostic efficacy and safety of Iomeprol versus other contrast agents like iohexol and iodixanol in pediatric populations. Early findings indicate that Iomeprol presents comparable image quality with a low incidence of adverse reactions.

  3. Evaluation of Reduced Volume Protocols
    An investigation (NCT04876543) examines whether lower volumes of Iomeprol can produce diagnostically equivalent images. Results aim to establish safer, cost-effective imaging protocols, especially for high-risk patients.

Ongoing Regulatory and Safety Evaluations

Regulatory agencies, including the FDA and EMA, continue to review post-marketing surveillance data to monitor rare adverse events such as allergic reactions and contrast-induced nephropathy (CIN). No significant safety signals have emerged recently, supporting Iomeprol’s continued clinical and commercial use.


Market Analysis

Current Market Dynamics

Market Size and Segmentation

The global contrast media market was valued at approximately USD 3.4 billion in 2022, with iodinated contrast agents constituting the largest segment, owing to their widespread utilization in CT and angiography. Iomeprol holds a significant share within this segment, primarily driven by its high image quality and safety profile.

Key Market Players

Major manufacturers include GE Healthcare, Bracco Diagnostics, and Guerbet. Bracco’s Omnipaque (iohexol), Guerbet’s Lipiodol (iodinated oil), and GE’s Omnipaque are close competitors to Iomeprol, which is marketed under various brand names such as Bracco’s Iomeron.

Geographical Market Distribution

The Asia-Pacific region, driven by expanding healthcare infrastructure, accounts for nearly 35% of the global contrast media market share. The North American market remains dominant due to advanced imaging infrastructure and high adoption rates. Europe follows, with increasing demand for safer contrast agents amid stringent safety regulations.

Regulatory Landscape

Regulatory approvals for Iomeprol are well-established across major markets. Its safety profile contributes to fewer restrictions, facilitating broader usage. However, regional variations in approval statuses and prescribing guidelines influence market penetration.

Competitive Advantages

Iomeprol’s advantages include:

  • High iodine concentration (370–370 mgI/mL), enabling excellent contrast enhancement at lower volumes.
  • Favorable safety profile, with low incidence of adverse reactions.
  • Compatibility with various imaging protocols, simplifying integration into existing workflows.

Market Challenges

Despite its strengths, Iomeprol faces challenges such as:

  • Competition from newer contrast agents with reduced nephrotoxicity.
  • Concerns over allergic reactions, particularly in iodine-sensitive patients.
  • Cost pressures prompting healthcare providers to prefer cost-effective alternatives.

Market Projection

Forecast Outlook (2023-2030)

The contrast media market is expected to grow at a CAGR of approximately 5.2% over the next eight years. The demand for iodinated contrast agents, including Iomeprol, will benefit from several macro trends:

  • Rising Cancer and Cardiovascular Disease Incidence: Increasing prevalence necessitates advanced imaging techniques, bolstering demand for contrast agents.
  • Technological Advancements: Development of low-volume, high-contrast agents tailored for specific populations, such as pediatric or renal-impaired patients.
  • Regulatory Approvals for New Indications: Expanded approval for uses such as vascular interventional procedures could enhance market opportunities.

Projected Revenue Growth

By 2030, the global Iomeprol market could approach USD 1.2 billion, driven by increased adoption in emerging markets and sustained demand in developed regions. A shift toward safer and more effective contrast agents could catalyze growth, but price sensitivity and regulatory hurdles may temper expansion.

Innovative Strategies

Manufacturers leveraging biosimilar development, integrating artificial intelligence for better diagnostic outcomes, and emphasizing safety profiles will likely outperform competitors. Additionally, expanding clinical trial evidence supporting Iomeprol’s safety in high-risk populations will enhance market confidence.


Conclusion

Iomeprol remains a vital component of the contrast media landscape, with ongoing clinical trials promising enhanced safety and expanded utility. Its market position benefits from its proven efficacy, though competition and safety concerns necessitate continuous innovation. The projected growth aligns with the broader increase in diagnostic imaging procedures, especially as healthcare systems worldwide seek safer, more effective contrast agents.


Key Takeaways

  • Clinical validation positions Iomeprol as a safe, effective contrast agent, with ongoing trials emphasizing its utility in renal impairment and pediatric populations.
  • Market dominance is supported by its high image enhancement capabilities and safety profile but faces headwinds from newer agents and cost considerations.
  • Regional growth potential is particularly strong in Asia-Pacific, owing to expanding healthcare infrastructure and diagnostic standards.
  • Future growth prospects hinge on clinical evidence demonstrating safety in high-risk populations and regulatory approval for new indications.
  • Innovation and safety remain paramount for sustaining and growing Iomeprol’s market share amid evolving healthcare demands.

FAQs

Q1: What are the main advantages of Iomeprol over other iodinated contrast agents?
A1: Iomeprol offers high iodine concentration for superior contrast enhancement, a favorable safety profile, and compatibility with various imaging protocols, making it a reliable choice for diverse diagnostic procedures.

Q2: Are there any recent safety concerns associated with Iomeprol?
A2: No significant recent safety issues have been reported. Post-marketing surveillance continues to monitor for rare adverse reactions such as allergic responses and contrast-induced nephropathy, with current data supporting its continued use.

Q3: How is the market for contrast agents expected to evolve over the next decade?
A3: The market is projected to grow steadily, driven by rising imaging procedures, technological innovations favoring lower doses, and expanding approvals for new indications, especially in emerging markets.

Q4: What are the primary challenges faced by Iomeprol manufacturers?
A4: Challenges include intense competition from newer, potentially safer contrast agents, regulatory pressures, pricing constraints, and concerns regarding contrast media reactions in sensitive patient groups.

Q5: How can clinical trials influence Iomeprol’s future market trajectory?
A5: Positive trial outcomes demonstrating safety and efficacy in high-risk groups and new indications can bolster confidence among clinicians and regulators, facilitating broader adoption and market expansion.


References

  1. [1] "Contrast Media Market Size, Share & Trends Analysis Report," Fortune Business Insights, 2022.
  2. [2] "ClinicalTrials.gov," U.S. National Library of Medicine, 2023.
  3. [3] "Global Iodinated Contrast Media Market," Grand View Research, 2022.
  4. [4] "Post-marketing Surveillance Reports," FDA, 2022.

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