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Benefits of the Use of Botox in the Treatment of Empty Nose Syndrome Syndrome

Primary Purpose

Empty Nose Syndrome, Atrophic Rhinitis

Status
Terminated
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Botulinum Toxin Type A
Sponsored by
Mayo Clinic
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Empty Nose Syndrome focused on measuring Empty nose syndrome, Over resection of turbinate, Atrophic rhinitis

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Any patient aged 18-65 years of age presenting with a known diagnosis of ENS who has no known allergies to Botox.

Exclusion Criteria:

  • Patients younger than 18 years or older than 65 years of age.
  • Patients with neuromuscular disorders or neuropathic diseases.
  • Patients with infection and or swelling at the site where Botox is to be injected.
  • Patients with known hypersensitivity to any ingredient in the drug formulation (botulinum toxin, human albumin)
  • Patients who are or plan to become pregnant within the time period in which the study will be conducted.
  • Patients who are nursing

Sites / Locations

  • Mayo Clinic

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Botulinum Toxin Type A

Arm Description

Treatment will be in the form of 10 Units of Botulinum Toxin Type A injected into the dilator nasalis muscle on each side of the nose.

Outcomes

Primary Outcome Measures

Mean Score of Sino Nasal Outcome Test 22 (SNOT 22)
The SNOT 22 is a validated measure of health related quality of life in sinonasal disease. It is a 22 item questionnaire with each item assigned a score ranging from 0-5. The total score may range from 0-110 and lower scores represent better health related quality of life.

Secondary Outcome Measures

Full Information

First Posted
August 8, 2008
Last Updated
March 18, 2016
Sponsor
Mayo Clinic
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1. Study Identification

Unique Protocol Identification Number
NCT00732680
Brief Title
Benefits of the Use of Botox in the Treatment of Empty Nose Syndrome Syndrome
Official Title
Prospective Case Series Evaluating Short and Long Term Benefits of the Use of Botox in the Treatment of Empty Nose Syndrome
Study Type
Interventional

2. Study Status

Record Verification Date
March 2016
Overall Recruitment Status
Terminated
Why Stopped
Lead investigator moved to a new medical center; study was stopped when he left.
Study Start Date
December 2008 (undefined)
Primary Completion Date
November 2009 (Actual)
Study Completion Date
November 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Mayo Clinic

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Empty Nose Syndrome patients suffer from disabling physical symptoms and considerable distress. To date there is no definitive cure for these symptoms. Established treatment modalities include saline irrigation, surgical implantation of materials or simply use of cotton wads/ silicon cones to simulate the resistive action to airflow of the resected turbinates. This study will research the effectiveness of a new treatment modality in the treatment of Empty Nose Syndrome. This novel treatment method involves the use of botulinum toxin type A (Botox).
Detailed Description
Background: Empty Nose Syndrome (ENS) is the term used to describe the condition resulting from over resection of nasal turbinate. Symptoms include depression, dysosmia, bleeding, discharge, crusting, dryness, dysosmia, and pain. Treatment modalities include adjunctive comfort measures (primarily irrigation), mechanical measures (Silicon cones, cotton wads) and surgical treatment (alloderm implants, plastipore cartilage grafts etc.) We will investigate a new method of treatment for ENS. This will involve injection of botulinum toxin type A into the dilator nasalis muscle thus collapsing the internal nasal valve to provide added resistance to air flow. Objective: To evaluate effectiveness of botulinum toxin type A in improving overall quality of life in ENS patients. Methods: ENS patients in this study will receive botulinum toxin type A along with adjunctive treatment which will include several measures. First of all, patients will be given a nasal rinse bottle and will be instructed to irrigate their noses twice a day as follows: Irrigate the nose 250cc (about 125cc each side) to clear the mucus. Stop and gently clear the nose. Irrigate the nose 250cc (about 125cc each side) once again. Sit quietly for 10 minutes. No blowing. Do not blow the nose for 2 hours. Patients will be asked to use sesame oil once a day to prevent drying of the nasal mucosa with further administration as needed. In addition they will advised to make certain lifestyle modifications that will include sleeping with a cool mist humidifier, drinking plenty of fluids and engaging in regular physical activity. Before and after treatment data will be obtained in the form of a breathing test and patient questionnaires that will measure changes in physical and mental health.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Empty Nose Syndrome, Atrophic Rhinitis
Keywords
Empty nose syndrome, Over resection of turbinate, Atrophic rhinitis

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
9 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Botulinum Toxin Type A
Arm Type
Experimental
Arm Description
Treatment will be in the form of 10 Units of Botulinum Toxin Type A injected into the dilator nasalis muscle on each side of the nose.
Intervention Type
Drug
Intervention Name(s)
Botulinum Toxin Type A
Other Intervention Name(s)
Botox
Intervention Description
10 Units of Botulinum Toxin Type A injected into the dilator nasalis muscle on each side of the nose.
Primary Outcome Measure Information:
Title
Mean Score of Sino Nasal Outcome Test 22 (SNOT 22)
Description
The SNOT 22 is a validated measure of health related quality of life in sinonasal disease. It is a 22 item questionnaire with each item assigned a score ranging from 0-5. The total score may range from 0-110 and lower scores represent better health related quality of life.
Time Frame
2 weeks after intervention, 2 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Any patient aged 18-65 years of age presenting with a known diagnosis of ENS who has no known allergies to Botox. Exclusion Criteria: Patients younger than 18 years or older than 65 years of age. Patients with neuromuscular disorders or neuropathic diseases. Patients with infection and or swelling at the site where Botox is to be injected. Patients with known hypersensitivity to any ingredient in the drug formulation (botulinum toxin, human albumin) Patients who are or plan to become pregnant within the time period in which the study will be conducted. Patients who are nursing
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Oren Friedman, M.D.
Organizational Affiliation
Mayo Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mayo Clinic
City
Rochester
State/Province
Minnesota
ZIP/Postal Code
55904
Country
United States

12. IPD Sharing Statement

Links:
URL
http://www.clinicaltrials.gov
Description
Online listing of the study with study details and contact information.
URL
http://www.fda.gov/
Description
FDA website. Great website for information on Botox.
URL
http://www.emptynosesyndrome.org/
Description
online blog of people with empty nose syndrome.
URL
http://clinicaltrials.mayo.edu
Description
Mayo Clinic Clinical Trials

Learn more about this trial

Benefits of the Use of Botox in the Treatment of Empty Nose Syndrome Syndrome

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