Skip to main content
OpenTrials
Completed

NCT Number: NCT00117611

Xolair in Patients With Chronic Sinusitis

The purpose of this study is to determine if treatment with the anti-IgE antibody, Xolair (omalizumab), will improve objective and subjective evidence of chronic sinusitis.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

The University of Chicago

Chicago, Illinois, 60637, United States

About this study

At its most basic level, sinusitis is defined as an inflammation of the lining membrane of the paranasal sinuses. Sinusitis affects all age groups, including 17% of people above the age of 65 years. On the basis of national population surveys and insurance-reimbursement claims, sinusitis is one of the most common health problems in the U.S. Thus, each year, billions of dollars are spent on direct medical costs for the treatment of this enigmatic illness.

Despite the enormous cost of the problem, there are no definite studies of treatment and management. There are some data indicating that intranasal steroids are effective, and recently Nasonex was approved for the treatment of nasal polyps. All other treatments are empirically based.

There is evidence that IgE antibodies play a role in chronic sinusitis. The investigators have shown that total IgE levels correlate with the severity of sinusitis, as assessed by CT scan. Staphylococcus enterotoxins cause local increases in total IgE in over 50% of nasal polyp patients. Allergies occur more frequently in patients with chronic sinusitis than in the general population. Elevations in total IgE have been shown to occur in patients with allergic fungal sinusitis and the levels of total IgE decrease with successful treatment. Thus, the investigators speculate that IgE contributes significantly to the pathogenesis of chronic sinusitis.

The purpose of this study is to determine if treatment with the anti-IgE antibody, Xolair, will improve objective and subjective evidence of chronic sinusitis.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Chronic sinusitis, as defined by symptoms for greater than 12 weeks, despite treatment
  • Paranasal sinus CT scan showing evidence of chronic sinusitis
  • Positive skin or RAST test to an inhalant allergen
  • Serum total IgE between 30 and 700 International Units/ml
  • Body weight less than 150 kg
  • Impaired quality of life, as measured by the Rhinosinusitis Disability Index (RSDI)

Exclusion criteria

  • Women of childbearing potential not using a contraception method(s) (birth control pills, Depo Provera, double barrier) as well as women who are breastfeeding
  • Known sensitivity to Xolair
  • Patients with severe medical condition(s) that, in the opinion of the investigator, prohibits participation in the study (heart, lung, kidney, neurological, oncologic or liver disease)
  • Use of any other investigational agent in the last 30 days
  • No measurable disability on the RSDI
  • Immunocompromised patients or patients with ciliary disorders

Treatment and study plan

Anti-IgE antibody omalizumab or placebo

Drug

given subcutaneously oce or twice monthly depending on dose

Other names: Xolair or placebo

Primary outcomes

  1. Mucosal thickness on CT scan

    Time frame: after 6 months of treatment

Secondary outcomes

  1. Rhinosinusitis Disability Index (RSDI)recorded monthly

    Time frame: 6 months

  2. A specific quality of life (QOL) measure, Sino-Nasal Outcome Test (SNOT 20)recorded monthly

    Time frame: 6 months

  3. A general health QOL measure (SF-36)

    Time frame: 6 months

  4. The number of sinusitis exacerbations requiring additional treatment

    Time frame: 6 months

  5. Nasal peak inspiratory flow

    Time frame: 6 months

  6. Symptoms of nasal discharge, nasal obstruction, facial pain and altered smell

    Time frame: 6 months

  7. Nasal lavage eosinophils

    Time frame: 6 months

  8. Nasal endoscopy score

    Time frame: 6 months

  9. The University of Pennsylvania Smell Identification Test (UPSIT)

    Time frame: 6 months

Sponsors and collaborators

Lead sponsor

University of Chicago

Other

Collaborators

  • Genentech, Inc.
  • Novartis Pharmaceuticals

Registry information

Official study title

Effects of Anti-IgE Antibody Omalizumab (Xolair) on Patients With Chronic Sinusitis and a Positive Allergen Test

Important dates

Study start
2005
Primary completion
2007
Study completion
2009
First posted
Jul 7, 2005
Registry last updated
Sep 30, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.