Skip to content
Clinical Trials – home

Gadoteridol: A Contrast Agent for MRI Scans

2 / 4
trials open to patients / all trials
8+
Countries

In short

Gadoteridol, also known by the brand name ProHance, is a gadolinium-based contrast agent used in magnetic resonance imaging (MRI) to enhance image quality and improve diagnostic accuracy. This article explores the use of gadoteridol in various clinical trials, focusing on its effectiveness, safety, and applications in different medical conditions, particularly in neurological imaging.

At a glance

Primary Uses
Enhancing MRI imaging for brain, spine, and whole-body scans
Key Conditions Studied
Brain metastases, multiple sclerosis, central nervous system diseases
Dosage
Typically 0.1 mmol/kg body weight, administered intravenously
Comparative Efficacy
Comparable to other gadolinium-based contrast agents like gadobutrol
Safety Profile
Generally well-tolerated; ongoing studies in pediatric populations
Imaging Parameters Improved
Contrast enhancement, border delineation, internal morphology of lesions
Clinical Benefits
Enhanced lesion detection, improved diagnostic confidence, better treatment planning
Ongoing Research
Use in various body regions, optimization of dosing, long-term safety

What is Gadoteridol?

Gadoteridol, also known by its brand name ProHance, is a type of contrast agent used in magnetic resonance imaging (MRI) scans. Contrast agents are substances given to patients before or during an MRI to help make certain parts of the body show up more clearly on the images. Gadoteridol belongs to a class of contrast agents called gadolinium-based contrast agents (GBCAs).

How Gadoteridol Works

Gadoteridol contains a rare earth element called gadolinium. When injected into the bloodstream, it circulates throughout the body and temporarily changes the magnetic properties of tissues. This allows the MRI scanner to create clearer and more detailed images of organs, blood vessels, and other structures inside the body.

Uses of Gadoteridol

Gadoteridol is primarily used to enhance MRI scans of the central nervous system (CNS), which includes the brain and spinal cord. It helps doctors detect and evaluate various conditions, such as:

  • Brain metastases: Cancerous tumors that have spread to the brain from other parts of the body
  • Multiple sclerosis (MS): A disease that affects the nervous system and can cause various neurological symptoms
  • Other brain and spinal cord disorders: Including tumors, infections, and inflammatory conditions

Gadoteridol can also be used for MRI scans of other parts of the body, such as the chest, abdomen, and pelvis, to help diagnose various conditions.

Administration and Dosage

Gadoteridol is typically given as an intravenous (IV) injection, which means it is injected directly into a vein. The standard dose is usually 0.1 mmol per kilogram of body weight. In some cases, a higher dose of 0.2 mmol/kg may be used. The exact dose and timing of the injection may vary depending on the specific type of MRI scan being performed and the patient's individual needs.

Safety and Side Effects

Gadoteridol is generally considered safe for most patients. However, like all medications, it can cause side effects in some people. Common side effects may include:

  • Headache
  • Nausea
  • Dizziness
  • Injection site reactions (such as pain or warmth)

Serious allergic reactions are rare but can occur. Patients with a history of allergies or kidney problems should inform their doctor before receiving gadoteridol.

Comparison to Other Contrast Agents

Several studies have compared gadoteridol to other gadolinium-based contrast agents, such as gadobutrol (Gadavist/Gadovist) and gadoquatrane. These studies aim to evaluate the effectiveness and safety of different contrast agents for various MRI applications.

Some key points from these comparisons include:

  • Gadoteridol and gadobutrol have shown similar effectiveness in enhancing MRI images of brain tumors.
  • Newer contrast agents, like gadoquatrane, are being developed with the goal of using lower doses of gadolinium while maintaining image quality.
  • The choice of contrast agent may depend on factors such as the specific body part being imaged, the patient's medical history, and the preference of the radiologist or healthcare provider.

Ongoing Research

Researchers continue to study gadoteridol and other contrast agents to improve MRI techniques and expand their applications. Some areas of ongoing research include:

  • Pediatric use: Evaluating the safety and effectiveness of gadoteridol in children under 2 years old.
  • Multiple sclerosis: Using gadoteridol to study blood flow changes in the brains of MS patients.
  • Brain metastases: Comparing different doses of gadoteridol for detecting and evaluating brain metastases.
  • New delivery methods: Investigating techniques like convection-enhanced delivery to administer contrast agents directly to brain tumors.

These ongoing studies aim to improve the diagnosis and treatment of various medical conditions using advanced imaging techniques with gadoteridol and other contrast agents.

Questions people often ask

Conditions where Gadoteridol is being studied

Each condition opens its own overview and trial list

Trials with Gadoteridol

Recruiting trials first

See all 4 →
Quick filters
  • Participants:Adults
Clinical Trials Concierge

Prefer not to search? Our Concierge searches the trials for you.

Tell us about your condition – we search every trial in Europe and connect you with the right site.

Legal notice · Published by CTIN POLAND sp. z o.o., ul. rtm. Witolda Pileckiego 67/109, 02-781 Warsaw, Poland · KRS 0001111334 · REGON 528919042 · NIP 9512598637

© 2026 Clinical Trials EU – European Clinical Trials Information Network

GDPR compliance, ISO 9001 and ISO 27001 certified (LL-C Certification)

On this site, “treatment” means an investigational medicine being studied in a clinical trial. Its safety and efficacy for the use being studied have not yet been confirmed, some participants may receive a placebo or a comparator medicine, and taking part does not guarantee any health benefit. The decision to take part is made by the doctor at the research site. This site is for information only and does not replace medical advice.

This service is not affiliated with the European Commission, the EMA, or the official CTIS system. Most information comes from publicly available international clinical-trial registries, supplemented by data from academic sites, national regulators and commercial sponsors. On this site, “treatment” and “therapy” mean a medicine being tested in a clinical trial. Its safety and effectiveness in the use being studied are not yet confirmed, some participants may receive a placebo or a comparator, and taking part does not guarantee a health benefit. The doctor at the research site decides who can take part. This site provides information, not medical advice. Certain content and visual elements on this website have been generated or enhanced using artificial intelligence (AI).