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Gore Tex Implants in the Treatment of Atrophic Rhinitis (RA)

This study has suspended participant recruitment.
(lack of new patients)
Sponsor:
ClinicalTrials.gov Identifier:
NCT00832403
First Posted: January 30, 2009
Last Update Posted: January 30, 2009
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Hospital Felicio Rocho
  Purpose

This is a retrospective study, involving patients with atrophic rhinitis, that underwent Gore tex® implants in the nasal fossa.

The Fetid Rhinitis or Atrophic Ozena is a chronic illness characterized by yellowish secretion in the initial phase and the other phases with fetid crusts and atrophy of the mucous bone covering. Diverse theories exist that try to explain the appearance of this pathology, such as: hereditary factors, immunological alterations, viral infection and nutritional lack. Currently, its etiology remains unknown. As there isn't any ideal treatment already established, this technique improves the options of treatment.

All patients have improved after the procedure.


Condition Intervention
Atrophic Rhinitis Other: implants of polytetrafluoroethylene in tha nasal fossa

Study Type: Observational
Study Design: Observational Model: Case-Only
Time Perspective: Retrospective
Official Title: Gore Tex Implants in the Treatment of Atrophic Rhinitis

Further study details as provided by Hospital Felicio Rocho:

Primary Outcome Measures:
  • improvement of fetid crusts and atrophy of the mucous bone covering [ Time Frame: after surgery recovery ]

Secondary Outcome Measures:
  • lack of side effects such as infection [ Time Frame: after the treatment ]

Enrollment: 5
Study Start Date: November 2006
Primary Completion Date: February 2008 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
polytetrafluoroethylene Other: implants of polytetrafluoroethylene in tha nasal fossa
surgical implants of polytetrafluoroethylene in the nasal fossa

Detailed Description:
Data about 5 patients that underwent surgery to implant polytetrafluoroethylene in the nasal fossa was collect. The symptoms and complications were described.
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   Child, Adult, Senior
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patients that were submit to surgery to treat atrophic rhinitis with implants in the nasal fossa.
Criteria

Inclusion Criteria:

  • Symptoms of atrophic rhinitis, with previous clinical treatment without good results

Exclusion Criteria:

  • Patients with mental illness
  Contacts and Locations
No Contacts or Locations Provided
  More Information

Responsible Party: Larissa Oliveira Lauriano, Hospital Felício Rocho
ClinicalTrials.gov Identifier: NCT00832403     History of Changes
Other Study ID Numbers: Rinite Atrófica cep/hfr
First Submitted: January 27, 2009
First Posted: January 30, 2009
Last Update Posted: January 30, 2009
Last Verified: January 2009

Keywords provided by Hospital Felicio Rocho:
atrophic rhinitis
implants
Polytetrafluoroethylene

Additional relevant MeSH terms:
Rhinitis
Atrophy
Rhinitis, Atrophic
Nose Diseases
Respiratory Tract Diseases
Respiratory Tract Infections
Otorhinolaryngologic Diseases
Pathological Conditions, Anatomical