Topical Bevacizumab for the Management of Recurrent Epistaxis in Patients With Hereditary Hemorrhagic Telangiectasia (HHT)

Part of paid clinical trials in San Diego, California.

Sponsor
University of California, San Diego
Study ID
NCT01397695
Phase
PHASE2
Status
Completed

Conditions

  • Hereditary Hemorrhagic Telangiectasia (HHT)

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Bevacizumab — DRUG
    The bevacizumab will then be sprayed by the treating physician in the clinic, under direct observation. Spray will be achieved by administering the bevacizumab through a mucosal atomization device. 0.1cc will be sprayed into both nares. Patients will then sit for 5 minutes, the application will be repeated for a total of 40 applications, thereby administering 50mgs into each nostril, a total of 100mgs into each patient. The 5 minute spacing has been arbitrarily chosen as sufficient time for 0.1cc of solution to be absorbed by the nasal mucosa. That will complete the treatment.

Study Details

Terence M. Davidson, MD is conducting a research study to find out more about the topical application of Avastin (proper chemical name is bevacizumab) in the treatment of epistaxis (nose bleeding) in patients with Hereditary Hemorrhagic Telangiectasia (HHT).

Key Dates

First listed
Jul 19, 2011
Start date
Jun 30, 2009
Status verified
Aug 2019
Primary completion
Jan 31, 2014
Completion
Jan 31, 2014

Study Design

Enrollment
20 participants (actual)
Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Experimental: bevacizumab

Primary Outcome Measure

Measurement of Epistaxis in Patients With HHT as Measured by the HHT Foundation Epistaxis Severity Score, Hematocrit, Hemoglobin and Serum Ferritin Levels. [ Time Frame: 1-2 years ]

Locations (1)

FacilityCityStateZIPSite coordinators
University of California, San Diego Medical CenterSan DiegoCalifornia92103-

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