Treatment of Hereditary Hemorrhagic Telangiectasia of the Nasal Mucosa by Intranasal Bevacizumab : Search for Effective Dose
EROSB
1 other identifier
interventional
20
1 country
1
Brief Summary
Epistaxis are present in over 90 % of patients with Rendu - Osler . They involve no significant difference 2 sexes. They often appear in childhood and adolescence and are present in three-quarters of patients at the age of 20 years. These epistaxis increasing in frequency and volume to the age of 60 in 2/3 of patients. Epistaxis are spontaneous , repetitive and recurring . They are highly variable in duration, intensity and frequency of occurrence . Some patients may have more than 40 monthly episodes with mean duration of 5 minutes of bleeding and chronic anemia and can sometimes acute anemia with transfusions need to be source. These epistaxis stigmatize patients and inevitably affect their quality of life and social skills . The various proposed ( cauterization , intra- mucosal injections, laser selective hémostatses , embolization or surgical dermoplasties ) allow for some short-term remissions . Bevacizumab is an antiangiogenic use in the treatment of colorectal cancers . It is also used in ophthalmology intravitreal to reduce vascular proliferation in glaucoma retinopathy and certain corneal neovascularization. In 2009, Prithviraj reported the use of bevacizumab injection to treat pulmonary arteriovenous malformations in a patient with Rendu - Osler . The result is doubly interesting including a saving action on epistaxis which decrease in frequency and duration. This communication prompted the authors to focus more on this medication. The product has been used in local submucosal injection intranasal laser was coupled with satisfactory results objectified by a decrease in the number of epistaxis , reducing blood transfusions and improved social lives. The use of local instillation bevacuzimab represents a way forward for the treatment of these epistaxis.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for phase_1
Started Dec 2014
Longer than P75 for phase_1
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 4, 2014
CompletedFirst Posted
Study publicly available on registry
June 6, 2014
CompletedStudy Start
First participant enrolled
December 15, 2014
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 8, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
December 8, 2021
CompletedApril 11, 2025
April 1, 2025
5.8 years
June 4, 2014
April 9, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
decrease of at least 50% of number of epistaxis in a month compared to the month before inclusion.
one month
Study Arms (1)
bevacizumab
EXPERIMENTALbevacizumab spray
Interventions
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- 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
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
CHU de Caen
Caen, 14033, France
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- phase 1
- Allocation
- NA
- Masking
- SINGLE
- Who Masked
- CARE PROVIDER
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
June 4, 2014
First Posted
June 6, 2014
Study Start
December 15, 2014
Primary Completion
October 8, 2020
Study Completion
December 8, 2021
Last Updated
April 11, 2025
Record last verified: 2025-04