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Can a cancer drug spray stop debilitating nosebleeds?

NCT ID NCT02157987

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jul 30, 2026 · Last updated Jul 31, 2026 · Updated 1 time

Summary

This trial tests whether a nasal spray containing bevacizumab, a drug typically used for cancer, can reduce frequent nosebleeds in people with hereditary hemorrhagic telangiectasia (HHT). The study enrolls 20 adults who have at least 10 nosebleeds per month. The goal is to see if the spray can cut the number of monthly nosebleeds by at least half.

What this could mean

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

Active substance
bevacizumab nasal spray
What this could lead to
If it works, this could offer a simple, non-surgical way to control frequent nosebleeds in people with HHT, improving quality of life.
What could go wrong
This is an early-phase trial with only 20 participants, so results may not apply broadly. The spray's effectiveness and safety are still unknown.

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 1/2

Runs two stages together: safety and dose first, then whether the treatment works.

Participants

20 people

The number who actually took part.

Started

Dec 2014

Finished

Dec 2021

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 to 70 years

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: * patients with Rendu-Osler-Weber disease * patients with iterative epistaxis (at least 10 per month) * patients without treatment for 3 months with usual techniques (for the epistaxis) * patients speaking french fluently * patients with written consents * affiliation to social security * women with effective contraception during the treatment and for 6 months after stopping Exclusion Criteria: General criteria: * Pregnant women, breastfeeding * Hypersensitivity to the active substance or any of its excipients * Hypersensitivity to the products of Chinese hamster ovary cells or other human or humanized recombinant antibodies * Inability to undergo medical monitoring due to reasons geographical, social or psychological * Patient under guardianship * Patient included in another biomedical research protocol Related to medical history criteria: * Uncontrolled hypertension ( systolic BP \> or = 150 mmHg and / or Diastolic BP \> or = 100 mmHg) * Thrombocytopenia \<100 G / L * Taking NSAIDs within ten days prior to inclusion * Anticoagulant therapy or thrombolytic within 28 days before inclusion * Tumor, genetic predisposition to bleeding, coagulopathy , patient receiving treatment full anticoagulant dose for an event thromboembolism prior to inclusion * Major surgery within 28 days prior to inclusion * History of thromboembolic disease within 6 months prior to enrollment * Arteriovenous malformation localized to the brain, liver or lung on scanner older than 5 years * History of heart failure * Patients with proteinuria / creatinine greater than 2g / g

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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 Caen

    Caen, 14033, France

More trials for these conditions

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