The Efficacy of Nasal Steroids in Treatment of Otitis Media With Effusion: Acomparative Study

Otitis Media With Effusion Clinical Trial

— Efficacy  

Official title:

The Efficacy of Nasal Steroids in Treatment of Otitis Media With Effusion: Acomparative Study

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT03491098
• Other study ID #: The Efficacy of Nasal Steroids
• Status: Not yet recruiting
• Phase: Early Phase 1
• First received: March 24, 2018
• Last updated: April 17, 2018
• Start date: May 15, 2018
• Est. completion date: March 1, 2020

Study information

• Verified date: April 2018
• Source: Assiut University
• Contact: Muteea M Bakuwairi, master
• Phone: 01148883026
• Email: bakuwairi2017[@]gmail.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Otitis media with effusion (OME) is defined as effusion in the middle ear without signs and symptoms of an acute infection. It is a leading cause of hearing impairment in children, and its early and proper management can avoid hearing and speech impairment, which can cause developmental delay in children.Although many conditions such as enlarged adenoids, cleft palate, Down syndrome, Kartagener syndrome, and nasopharyngeal neoplasm are related to the role of eustachian tube (ET) dysfunction in the pathogenesis of OME, allergic, immunologic, and infectious factors have also been claimed. Treatment of OME is still a controversial issue, as conventional treatment approaches fail to provide satisfactory and permanent relief of otologic symptoms.There is lack of proven effectiveness of the commonly given treatments, such as antibiotics, decongestants, and antihistamines, which are potentially harmful and have disadvantages. Few in those studies,investigated topical intranasal steroid for OME treatment,and in those studies, the duration of intranasal steroid application was short and there was no hearing evaluation.

Description:

The aim of this study is to assess the efficacy of nasal steroids in management of OME by comparing its results with that of oral steroids and that of nasal saline spray.

Sixty patients (4-12) years aged children with OME over a period for two months will be included in this study. Informed written consent will obtained from the parents of patient studied after explanation of the research purpose.

Patient diagnosed clinically to have OME with type B tympanogram and conductive hearing loss will be enrolled in our study.

Exclusion criteria:

1. Patients previously managed by ventilation tube.

2. Those who had cleft palate. The patients were divided into three equal groups. In group 1, 20 patients will be received steroids spray, for. 2 months In group 2, 20 patients will be received steroids for 1 month In group 3, 20 patients will be receive hypertonic sea water solution Otoscopic examination, basic audiological evaluation including pure tone audiometry, and immittancemetry will be performed before treatment and repeated at 3 and 6 months after treatment. The evaluation was performed using ORBITR 922 VERSION2 . Examiners will be blinded to the type of treatment.

Tympanometry results were distinguished into four grades as classified by El-Anwar et al12:

type A, normal curve (pressure 50/_99 H2O); type C1 (negative pressure _100/_199 mm H2O); type C2 (negative pressure _200/_394 mm H2O); type B (flat curve).2,3,11 The average hearing thresholds at 500 Hz and 1, 2, and 4 kHz were used in the statistical comparison.

Follow-up clinical examinations were done once per week for 3 weeks, at the end of treatment. The efficacy of nasal steroid for management of OME was compared with that of oral steroid and that of nasal sinomarin spray as placebo.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 60
• Est. completion date: March 1, 2020
• Est. primary completion date: April 30, 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 4 Years to 12 Years

Eligibility

Inclusion Criteria:

• Sixty patients (4-12) years aged children with OME over a period for two months.

Exclusion Criteria:

• Patients previously managed by ventilation tube.

• Those who had cleft palate.

Related Conditions & MeSH terms

• Otitis
• Otitis Media
• Otitis Media with Effusion

Intervention

Drug:
• Mometasone Furoate spray
Mometasone Furoate spray one puff in each nostril daily for 8 weeks hypertonic sea water solution spray one puff in each nostril daily for (8) weeks.
• prednisolone sodium phosphate 15mg
three times per day for 1 week then gradual withdrawal over 2 weeks
• hypertonic sea water solution spray
one puff in each nostril daily for 8 weeks

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Muteea Mubark Salmen Bakuwiri

References & Publications (5)

Bernstein JM, Lee J, Conboy K, Ellis E, Li P. Further observations on the role of IgE-mediated hypersensitivity in recurrent otitis media with effusion. Otolaryngol Head Neck Surg. 1985 Oct;93(5):611-5. — View Citation

Ho WK, Wei WI, Yuen AP, Hui Y, Wong SH. Otorrhea after grommet insertion for middle ear effusion in patients with nasopharyngeal carcinoma. Am J Otolaryngol. 1999 Jan-Feb;20(1):12-5. — View Citation

Tang NL, Choy AT, John DG, van Hasselt CA. The otological status of patients with nasopharyngeal carcinoma after megavoltage radiotherapy. J Laryngol Otol. 1992 Dec;106(12):1055-8. — View Citation

Tomonaga K, Kurono Y, Chaen T, Mogi G. Adenoids and otitis media with effusion: nasopharyngeal flora. Am J Otolaryngol. 1989 May-Jun;10(3):204-7. — View Citation

Yousaf M, Inayatullah, Khan F. Medical versus surgical management of otitis media with effusion in children. J Ayub Med Coll Abbottabad. 2012 Jan-Mar;24(1):83-5. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Clinical examination:Hearing loss	Hearing loss,0=no symptoms,1= present 2 weeks ,3=present daily,4=always present,	2 weeks evaluation for 2 months
Primary	Clinical examination:Nasal obstruction	Nasal obstruction,0=no symptoms,1= present 2 weeks ,3=present daily,4=always present,	2 weeks evaluation for 2 months
Primary	Full E.N.T history	Snoring ,sleep apnea ,difficult suckling in infants,anterior nasal discharge and conductive hearing loss.	2 weeks evaluation for 2 months