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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05545345
Other study ID # 2022-AdOME
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date September 2022
Est. completion date September 2025

Study information

Verified date September 2022
Source Eye & ENT Hospital of Fudan University
Contact Huiqian Yu, PhD
Phone 86-13636423139
Email yhq925@163.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study aims to verify the efficacy of adjuvant adenoidectomy for children with chronic OME who become candidates for tympanostomy tube placement, and explore potential factors associated with the efficacy of adjuvant adenoidectomy.


Description:

Otitis media with effusion is a common condition in children, and tympanostomy tube placement is the first-line treatment for those who requires surgical interventions. Adenoidectomy proves to be helpful to children over 4 years old, but the risks of adjuvant surgery is believed to somehow offset its benefits. This study is meant to verify if concurrent adenoidectomy provides extra benefits in resolving MEE, reducing AOM, and improving hearing and patients' quality of life to children who become candidates for TT.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 380
Est. completion date September 2025
Est. primary completion date September 2025
Accepts healthy volunteers No
Gender All
Age group 4 Years to 12 Years
Eligibility Inclusion Criteria: - 1. Children 4-12 years of age. - 2. Diagnosed with chronic OME. Diagnostic criteria: I. Middle ear effusion detected by otoscopy; II. Type B or C tympanograms; III. Symptoms/signs of OME persisted for >3 months; - 3. Documented hearing loss =20dB (average threshold of 500Hz, 1000Hz and 2kHz in pure tone audiometry). - 4. Adenoid hypertrophy (A/N ratio> 0.5 in lateral radiography of the nasopharynx). - 5. Informed consent given by the patients and their guardians. Exclusion Criteria: 1. Cleft palate or other systemic disorders. 2. Patients are diagnosed with other nose, sinuses or ear diseases that are eligible for surgical treatment. 3. Patients are diagnosed with OSAHS, tonsil hypertrophy =IIĀ° or scheduled for tonsillectomy. 4. History of tympanostomy tube placement. 5. Infection of the upper respiratory tract or acute rhinosinusitis over the past 7 days. 6. Sensorineural hearing loss. 7. Other situations that the investigators find unsuitable for the trial.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
tympanostomy tube placement
An incision will be made in the the tympanic membrane, through which a ventilation tube will be inserted.
adenoidectomy
The adenoid is resected transorally under a 70° endoscope with microdebrider or coblator until torus tubarius and choanae are completely revealed.

Locations

Country Name City State
n/a

Sponsors (3)

Lead Sponsor Collaborator
Eye & ENT Hospital of Fudan University Children's Hospital of Fudan University, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine

Outcome

Type Measure Description Time frame Safety issue
Primary Recurrence rate Rate of OME recurrence 1 year after tube removal
Primary Rate of repeated tube placement proportion of patients who need repeated tube insertion 1 year after tube removal
Secondary AOM attacks The number of acute otitis media attacks 1 year after tube removal
Secondary Otorrhea Rate of Otorrhea 2 years after tube insertion
Secondary Pure tone audiometry Change of pure tone audiometry thresholds compared with baseline 2 years after tube insertion
Secondary Otitis Media-6 and Pediatric Sleep Questionnaire Change of questionnaire score. Otitis Media-6 score ranges from 6 to 42, and higher scores mean worse outcomes. Pediatric Sleep Questionnaire score ranges from 0 to 22, and higher scores mean worse outcomes. 2 years after tube insertion
Secondary Complications Complications related to interventions of this study 2 years after tube insertion
Secondary Costs of OME-related visits and treatment Medical expenses associated with OME Through study completion, an average of 2 years
See also
  Status Clinical Trial Phase
Withdrawn NCT03347461 - Otiprio Versus Ciprodex Tympanostomy Tube Outcomes Phase 4
Completed NCT02539654 - Pediatric Pharmacokinetic (PK) Study of EXE844 Otic Suspension in Otitis Media at the Time of Tympanostomy Tube Insertion (OMTT) Phase 1
Completed NCT02432105 - Safety and Efficacy of EXE844 Otic Suspension in Otitis Media at Time of Tympanostomy Tube Insertion (OMTT) Phase 3
Completed NCT02436304 - Safety and Efficacy of EXE844 Otic Suspension in Otitis Media at Time of Tympanostomy Tube Insertion (OMTT) - Study 2 Phase 3
Completed NCT06100159 - Short-term Effects of Ventilation Tubes in Children With Chronic Otitis Media With Effusion N/A