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The Polymerase Chain Reaction (PCR) Analysis of Nasal Polyps for Fungal DNA

This study is currently recruiting participants.
Verified by University of California, San Francisco, August 2008

Sponsors and Collaborators: University of California, San Francisco
Environmental Protection Agency (EPA)
Information provided by: University of California, San Francisco
ClinicalTrials.gov Identifier: NCT00739921
  Purpose

The objective of this study is to determine whether the amount or type of fungal DNA present in the nose and home environment can be correlated with the outcomes of the following quality of life (QOL) instruments: Medical Outcomes Study 36-item Short Form (SF-36) and the Sino-Nasal Outcomes Study - 20 Questions (SNOT-20).


Condition Intervention
Sinusitis
Nasal Polyps
Procedure: Nasal swab under endoscopic guidance

MedlinePlus related topics:   Molds    Sinusitis   

ChemIDplus related topics:   Tetracaine    Viractin    Phenylephrine    Guaifenesin    Naphazoline    Naphazoline hydrochloride    Oxymetazoline    Oxymetazoline hydrochloride    Phenylephrine hydrochloride    Phenylpropanolamine    Phenylpropanolamine hydrochloride    Salicylsalicylic acid    Sodium salicylate   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Diagnostic, Open Label, Parallel Assignment
Official Title:   PCR Analysis of Nasal Polyps for Fungal DNA

Further study details as provided by University of California, San Francisco:

Primary Outcome Measures:
  • Quality of life (QOL) instruments: Medical Outcomes Study 36-Item Short Form (SF-36) and the Sino-Nasal Outcomes Study- 20 questions (SNOT-20). [ Time Frame: During the course of outpatient visit ] [ Designated as safety issue: No ]

Estimated Enrollment:   187
Study Start Date:   June 2006
Estimated Study Completion Date:   October 2009
Estimated Primary Completion Date:   July 2009 (Final data collection date for primary outcome measure)

Arms Assigned Interventions
1: Experimental
Patients with sinusitis compared to patients without.
Procedure: Nasal swab under endoscopic guidance
Patients with and without sinusitis will have a nasal swab taken under endoscopic guidance from their nose (middle meatus) after the application of pontocaine and neosynephrine spray. The swab will be refrigerated and analyzed using PCR to detect and speciate fungus.

Detailed Description:

The objective of this study is to determine whether the amount or type of fungal DNA present in the nose and home environment can be correlated with the outcomes of the following quality of life (QOL) instruments: Medical Outcomes Study 36-item Short Form (SF-36) and the Sino-Nasal Outcomes Study - 20 Questions (SNOT-20).

The study design involves case control Polymerase Chain reaction (PCR) analysis of nasal mucosal swabs and home vacuum cleaner bags in patients with sinusitis and normal controls.

The hypothesis is that the quantity and type of fungal DNA present in the nose and home environment are directly correlated with quality of life. Our research aims to both quantify the amount of fungi present in the nasal mucosa as well as to measure the severity of the patient's chronic rhinosinusitis (CRS) as a function of SNOT-20 and SF-36 outcomes questionnaires. We hypothesize that the amount and type of fungi present in the nose and home environment will correlate with the severity of the patients' symptoms of CRS.

  Eligibility
Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes

Criteria

Inclusion Criteria:

  • Subjects with no sinus disease and subjects with chronic rhinosinusitis.

Exclusion Criteria:

  • Immunocompromise
  • Pregnancy
  • Minors
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00739921

Contacts
Contact: Wendy Ma     415-353-2870     wma@ohns.ucsf.edu    
Contact: Andrew Murr, MD     415-353-2870     ahmurr@ohns.ucsf.edu    

Locations
United States, California
University of California, San Francisco, Dept of Otolaryngology-HNS     Recruiting
      San Francisco, California, United States, 94143
      Contact: Wendy Ma     415-353-2870     wma@ohns.ucsf.edu    
      Contact: Andrew Murr, MD     415-353-2870     ahmurr@ohns.ucsf.edu    
      Principal Investigator: Andrew Murr, MD            
      Sub-Investigator: Andrew Goldberg, MD, MSCE            

Sponsors and Collaborators
University of California, San Francisco
Environmental Protection Agency (EPA)

Investigators
Principal Investigator:     Andrew Murr, MD     University of California, San Francisco    
  More Information


Publications:

Responsible Party:   University of California, San Francisco ( Andrew Murr, MD )
Study ID Numbers:   H9272-26987-04
First Received:   August 19, 2008
Last Updated:   August 20, 2008
ClinicalTrials.gov Identifier:   NCT00739921
Health Authority:   United States: Institutional Review Board

Keywords provided by University of California, San Francisco:
PCR Analysis  
Allergic fungal sinusitis  
Chronic rhinosinusitis  
Nasal Polyps  

Study placed in the following topic categories:
Pathological Conditions, Anatomical
Otorhinolaryngologic Diseases
Salicylsalicylic acid
Sodium Salicylate
Polyps
Sinusitis
Tetracaine
Nasal Polyps
Naphazoline
Oxymetazoline
Respiratory Tract Diseases
Respiratory Tract Infections
Guaifenesin
Phenylephrine
Phenylpropanolamine

Additional relevant MeSH terms:
Paranasal Sinus Diseases
Nose Diseases

ClinicalTrials.gov processed this record on October 15, 2008




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