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Effectiveness of Sulfamethoxazole-trimethoprim in the Treatment of Chronic Otitis Media

Primary Purpose

Chronic Otitis Media

Status
Completed
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Sulfamethoxazole-trimethoprim
Placebo
Sponsored by
UMC Utrecht
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Otitis Media

Eligibility Criteria

1 Year - 12 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria: age between 1 and 12 years otorrhea for more than 3 months Exclusion Criteria: cholesteatoma known immune deficiency other than IgA or IgG2 Down's syndrome craniofacial anomalies cystic fibrosis immotile cilia syndrome allergy to sulfamethoxazole-trimethoprim continuous use of sulfamethoxazole-trimethoprim for more than six weeks in the past six months

Sites / Locations

  • Wilhelmina Children Hospital, University Medical Center Utrecht

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Active Comparator

Arm Label

placebo

Sulfamethoxazole-trimethoprim

Arm Description

Outcomes

Primary Outcome Measures

Number of Participants With Otomicroscopic Signs of Otorrhea in Either Ear
The primary endpoint was otomicroscopic signs of otorrhea in either ear in the presence of a tympanostomy tube or tympanic membrane perforation at 6 and 12 weeks and 1 year follow-up. At these follow-up moments the participants were checked for the presence of otorrhea using an otomicroscope.

Secondary Outcome Measures

Number of Patients Who Used Additional Antibiotic Eardrops Between 6 to 12 Week Follow-up
Parents kept a diary of study medication and additional medication used for their child's' ear disease, including eardrops. These data were collected at the follow-up visits.
Number of Patients Who Used Additional Antibiotic Eardrops Between 12 Weeks to 1 Year Follow-up
Parents kept a diary of study medication and additional medication used for their child's' ear disease, including eardrops. These data were collected at the follow-up visits.
Number of Patients Who Used Systemic Antibiotics Other Than the Study Medication Between 6 and 12 Weeks Follow-up.
Parents kept a diary of study medication and additional medication used for their child's' ear disease, including additional use of systemic antibiotics other than the study medication. These data were collected at the follow-up visits.
Number of Patients Who Used Systemic Antibiotics Other Than the Study Medication Between 12 Weeks and 1 Year Follow-up.
Parents kept a diary of study medication and additional medication used for their child's' ear disease, including additional use of systemic antibiotics other than the study medication. These data were collected at the follow-up visits.
Number of Patients Who Underwent Ear Nose and Throat Surgery Between 12 Weeks and 1 Year Follow-up.
After 12 weeks follow-up irrespective of the presence or absence of otorrhea the study medication was discontinued. After the first 12 weeks local otorhinolaryngologists and paediatricians were free to manage symptoms of otorrhea according to their regular practice. Parents kept a diary between 12 weeks and 1 year follow-up where Ear Nose and Throat Surgery was noted. This outcome describes the number of patients who underwent Ear Nose and Throat Surgery between 12 weeks and 1 year follow-up.

Full Information

First Posted
September 12, 2005
Last Updated
June 8, 2012
Sponsor
UMC Utrecht
Collaborators
Dutch Health Care Insurance Board
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1. Study Identification

Unique Protocol Identification Number
NCT00189098
Brief Title
Effectiveness of Sulfamethoxazole-trimethoprim in the Treatment of Chronic Otitis Media
Official Title
Effectiveness of Sulfamethoxazole-trimethoprim in the Treatment of Chronic Otitis Media
Study Type
Interventional

2. Study Status

Record Verification Date
April 2012
Overall Recruitment Status
Completed
Study Start Date
February 2003 (undefined)
Primary Completion Date
June 2006 (Actual)
Study Completion Date
November 2006 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
UMC Utrecht
Collaborators
Dutch Health Care Insurance Board

4. Oversight

5. Study Description

Brief Summary
Chronic suppurative otitis media is one of the most common chronic infections in children worldwide. Symptoms include otorrhea, otalgia and hearing loss. In many countries, it is treated primarily with antibiotics; in other countries such as the Netherlands a surgical approach, such as a tonsillectomy, adenoidectomy, placement or removal of tympanostomy tubes or a tympanomastoidectomy is preferred. There is however, no agreement on the management of this disease. The purpose of this study is to determine the effectiveness of treatment with sulfamethoxazole-trimethoprim for 6-12 weeks in children suffering from chronic otitis media and otorrhea.
Detailed Description
Chronic suppurative otitis media is one of the most common chronic infections in children worldwide. Symptoms include otorrhea, otalgia and hearing loss. In many countries it is treated primarily with antibiotics; in other countries such as the Netherlands a surgical approach, such as a tonsillectomy, adenoidectomy, placement or removal of tympanostomy tubes or a tympanomastoidectomy is preferred. There is however, no agreement on the management of this disease. Co-trimoxazole is an inexpensive antibiotic and tolerated well by children, also when long treatment regimens or prophylaxis is necessary. A previously performed retrospective study of 48 children who were referred to the pediatric department of otorhinolaryngology in the UMC Utrecht because of "therapeutic resistant" otorrhea showed promising results; after 3 months follow-up, 52% of the patients were otorrhea free, 25% had otorrhea incidentally and 23% showed no signs of improvement. Therefore, the treatment of chronic otitis media with sulfamethoxazole-trimethoprim for a minimum of six weeks is promising and might be a good alternative to surgical treatment. The purpose of this study is to determine the effectiveness of treatment with sulfamethoxazole-trimethoprim during 6-12 weeks in children with chronic otitis media and otorrhea for more than 12 weeks.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Otitis Media

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
101 (Actual)

8. Arms, Groups, and Interventions

Arm Title
placebo
Arm Type
Placebo Comparator
Arm Title
Sulfamethoxazole-trimethoprim
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
Sulfamethoxazole-trimethoprim
Intervention Description
18 mg/kg, two times a day
Intervention Type
Drug
Intervention Name(s)
Placebo
Primary Outcome Measure Information:
Title
Number of Participants With Otomicroscopic Signs of Otorrhea in Either Ear
Description
The primary endpoint was otomicroscopic signs of otorrhea in either ear in the presence of a tympanostomy tube or tympanic membrane perforation at 6 and 12 weeks and 1 year follow-up. At these follow-up moments the participants were checked for the presence of otorrhea using an otomicroscope.
Time Frame
6, 12 weeks and 1 year follow-up.
Secondary Outcome Measure Information:
Title
Number of Patients Who Used Additional Antibiotic Eardrops Between 6 to 12 Week Follow-up
Description
Parents kept a diary of study medication and additional medication used for their child's' ear disease, including eardrops. These data were collected at the follow-up visits.
Time Frame
Between 6 to12 week follow up
Title
Number of Patients Who Used Additional Antibiotic Eardrops Between 12 Weeks to 1 Year Follow-up
Description
Parents kept a diary of study medication and additional medication used for their child's' ear disease, including eardrops. These data were collected at the follow-up visits.
Time Frame
between 12 weeks to 1 year follow-up
Title
Number of Patients Who Used Systemic Antibiotics Other Than the Study Medication Between 6 and 12 Weeks Follow-up.
Description
Parents kept a diary of study medication and additional medication used for their child's' ear disease, including additional use of systemic antibiotics other than the study medication. These data were collected at the follow-up visits.
Time Frame
between 6 and 12 weeks follow-up
Title
Number of Patients Who Used Systemic Antibiotics Other Than the Study Medication Between 12 Weeks and 1 Year Follow-up.
Description
Parents kept a diary of study medication and additional medication used for their child's' ear disease, including additional use of systemic antibiotics other than the study medication. These data were collected at the follow-up visits.
Time Frame
between 12 weeks and 1 year follow-up
Title
Number of Patients Who Underwent Ear Nose and Throat Surgery Between 12 Weeks and 1 Year Follow-up.
Description
After 12 weeks follow-up irrespective of the presence or absence of otorrhea the study medication was discontinued. After the first 12 weeks local otorhinolaryngologists and paediatricians were free to manage symptoms of otorrhea according to their regular practice. Parents kept a diary between 12 weeks and 1 year follow-up where Ear Nose and Throat Surgery was noted. This outcome describes the number of patients who underwent Ear Nose and Throat Surgery between 12 weeks and 1 year follow-up.
Time Frame
between 12 weeks and 1 year follow-up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Year
Maximum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: age between 1 and 12 years otorrhea for more than 3 months Exclusion Criteria: cholesteatoma known immune deficiency other than IgA or IgG2 Down's syndrome craniofacial anomalies cystic fibrosis immotile cilia syndrome allergy to sulfamethoxazole-trimethoprim continuous use of sulfamethoxazole-trimethoprim for more than six weeks in the past six months
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anne GM Schilder, MD, PhD
Organizational Affiliation
University Medical Centre Utrecht, Department of Pediatric Otorhinolaryngology
Official's Role
Study Director
Facility Information:
Facility Name
Wilhelmina Children Hospital, University Medical Center Utrecht
City
Utrecht
ZIP/Postal Code
3508AB
Country
Netherlands

12. IPD Sharing Statement

Citations:
PubMed Identifier
17473089
Citation
van der Veen EL, Rovers MM, Albers FW, Sanders EA, Schilder AG. Effectiveness of trimethoprim/sulfamethoxazole for children with chronic active otitis media: a randomized, placebo-controlled trial. Pediatrics. 2007 May;119(5):897-904. doi: 10.1542/peds.2006-2787.
Results Reference
result
PubMed Identifier
19297377
Citation
van der Veen EL, Schilder AG, Timmers TK, Rovers MM, Fluit AC, Bonten MJ, Leverstein-van Hall MA. Effect of long-term trimethoprim/sulfamethoxazole treatment on resistance and integron prevalence in the intestinal flora: a randomized, double-blind, placebo-controlled trial in children. J Antimicrob Chemother. 2009 May;63(5):1011-6. doi: 10.1093/jac/dkp050. Epub 2009 Mar 18.
Results Reference
derived

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Effectiveness of Sulfamethoxazole-trimethoprim in the Treatment of Chronic Otitis Media

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