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Study reveals artery stiffness from common cancer drug

NCT ID NCT04813913

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study looked at how bevacizumab, a drug used to treat advanced colorectal cancer, affects the stiffness of arteries. Researchers measured artery stiffness in 13 patients before and after 4 months of treatment. The goal was to better understand the drug's cardiovascular side effects, like high blood pressure, and how they relate to cancer treatment.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
bevacizumab (Avastin) combined with chemotherapy
What this could lead to
If successful, this could help doctors understand and manage the cardiovascular side effects of bevacizumab in colorectal cancer patients.
What could go wrong
This is a small, completed Phase 4 study with only 13 participants, so results may not apply broadly. It focuses on measuring artery stiffness, not on improving cancer outcomes.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Phase 4

Runs after approval, following long-term safety and how well the treatment works in everyday use.

Participants

13 people

The number who actually took part.

Started

May 2019

Finished

Jul 2022

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Patient at least 18 years old, * Patient with colorectal cancer of the adenocarcinoma type, stage IV, histologically confirmed, mutated or wild tumor RAS status (exons 2, 3 and 4 of the KRAS and NRAS genes), mutated or wild BRAF status, naive in antineoplastic treatment * Patient eligible to start systemic carcinological treatment including bevacizumab in combination with chemotherapy based on IV fluoropyrimidine, * General condition WHO grade less than or equal to 3, * Life expectancy greater than 4 months, * Patient who has read and understood the information letter and signed the consent form, * Patient affiliated to a social security scheme, * Effective contraception (see WHO definition) in women of childbearing age (negative pregnancy test). For postmenopausal women, a confirmatory diagnosis should be obtained (amenorrhea not medically induced for at least 12 months before the inclusion visit). Exclusion Criteria: * Previous exposure to anti-VEGF, * Exposure to treatment for metastatic disease in the 12 months prior to inclusion, * Other histologically proven neoplasia not considered in complete remission or considered in complete remission for less than two years, * Bilateral carotid breath, * Absence of peripheral pulse of the two upper limbs, * Contraindication to AVASTIN 25 mg / ml concentrate for solution for infusion: * Hypersensitivity to the active substance or to any of the excipients, * Hypersensitivity to Chinese hamster ovarian cell products or other human or humanized recombinant antibodies, * Patients: * having undergone a major surgical intervention in the 28 days preceding the inclusion or as long as the surgical wound is not completely healed, * Unhealed ulcer or wound, * having uncontrolled pre-existing hypertension (PAS\> or = 170 mm Hg after three repeated measurements at rest), * having a history of arterial thromboembolism (transient ischemic attack (TIA), cardiovascular accident (stroke) or recent (\<6 months) and / or symptomatic myocardial infarction (MI) * having had an invasive dental procedure in the 28 days preceding inclusion, * with known proteinuria\> 2g / 24h or in whom proteinuria\> 2g / 24h is discovered in the case of a positive urine strip 3+ for proteins (excluding urinary tract infection), * on aspirin\> 325 mg / d, * with a colonic prosthesis in place, * Systemic treatment with anti-EGFR monoclonal antibodies, * Presence or history of lymphedema of the bilateral upper limbs, * Patient with poor understanding of spoken or written French, * Patient deprived of liberty by an administrative or judicial decision or patient placed under the protection of justice, under guardianship or curatorship, * Pregnant or lactating woman or wishing to breastfeed within 6 months after the last administration of the treatment, * Patient participating in another drug trial / having participated in another drug trial within 30 days of inclusion, * History of illness or psychological or sensory abnormality likely to prevent the subject from fully understanding the conditions required for his participation

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • CHU de ROUEN

    Rouen, France

More trials for these conditions

Other studies related to the condition(s) this trial covers.