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A Prospective, Randomized, Controlled Clinical Study of BET Combined With Tympanostomy Tube Insertion in the Treatment of Intractable OME After Radiotherapy for NPC

Primary Purpose

Otitis Media With Effusion After Nasopharyngeal Carcinoma

Status
Recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Balloon Eustachian Tuboplasty with Tympanostomy Tube Insertion
Tympanostomy Tube Insertion
Sponsored by
Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Otitis Media With Effusion After Nasopharyngeal Carcinoma focused on measuring Balloon Eustachian Tuboplasty, Tympanostomy Tube Insertion, Otitis Media With Effusion, Nasopharyngeal Carcinoma

Eligibility Criteria

15 Years - 70 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • patients clinically diagnosed OME after radiotherapy for NPC (diagnostic criteria: have fluid drained from tympanic cavity during tympanocentesis) , who had completed radiotherapy for ≥6 months, and had failed to respond after two or more times of tympanocentesis
  • Eustachian Tube Dysfunction Questionnaire score greater than 14
  • clinical findings of a retracted drum
  • fluid behind the drum
  • tympanometry type B or C results
  • patients volunteered to participate in the study and signed the informed consent
  • patients volunteered to bear the corresponding costs of surgery and consumables.

Exclusion Criteria:

  • NPC recurrence or other malignant tumor after radiotherapy
  • a perforated tympanic membrane
  • the presence of a ventilation tube
  • a period of less than six months following the final radiotherapy treatment
  • clear diagnosis of Eustachian ostium atresia or nasal obstruction diseases, such as severe deviated nasal septum, nasal polyp, choanal atresia, osteoradionecrosis of skull base after radiotherapy, etc.
  • patients with severe underlying diseases could not tolerate general anesthesia
  • patients who could not cooperate (including poor hearing and radiation encephalopathy)
  • patients with other middle ear diseases, such as middle ear cholesteatoma, osteoradionecrosis of temporal bone after radiotherapy, etc.
  • severe deglutition disorders
  • cleft palate

Sites / Locations

  • Sun Yat-sen Memorial Hospital, Sun Yat-sen UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Balloon Eustachian Tuboplasty with Tympanostomy Tube Insertion

Tympanostomy Tube Insertion

Arm Description

Outcomes

Primary Outcome Measures

changes in air pressure (Tympanogram)
Tympanogram, which measures the movement of the tympanic membrane in response to changes in air pressure, is classified by types - Type A, B and C. Each classification indicates a range that falls between normal and abnormal.

Secondary Outcome Measures

Incidence of Otitis Media
The number of days of ear discharges or otorrhoea in a 6-month period of tube retention
Incidence of Slippage of Ventilation Tube
The number of times the ventilation tube falls off in a 6-month period of tube retention
Eustachian Tube Dysfunction Questionnaire (ETDQ-7)
The ETDQ-7 tool is used to assess the symptoms of Otitis Media With Effusion (OME), which consists of seven items with a scale of graduated responses ranging from 1 (No Problem) to 7 (Severe Problem), and 4 would correspond to a Moderate Problem. If the total score is more than 14, it is considered that there is eustachian tube dysfunction. The average post-operative ETDQ-7 score is less than 2.1 or decrease > 0.5 (minimal clinically important difference=0.5), it is considered that the eustachian tube function is improved.
Hearing gap
It is the change of air-bone conduction difference between pre-operation and post-operation, which is measured by Pure-Tone Audiometry.

Full Information

First Posted
June 1, 2022
Last Updated
July 7, 2022
Sponsor
Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
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1. Study Identification

Unique Protocol Identification Number
NCT05449184
Brief Title
A Prospective, Randomized, Controlled Clinical Study of BET Combined With Tympanostomy Tube Insertion in the Treatment of Intractable OME After Radiotherapy for NPC
Official Title
A Prospective, Randomized, Controlled Clinical Study of Balloon Eustachian Tuboplasty Combined With Tympanostomy Tube Insertion in the Treatment of Intractable Otitis Media With Effusion After Radiotherapy for Nasopharyngeal Carcinoma
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Recruiting
Study Start Date
June 14, 2022 (Actual)
Primary Completion Date
June 1, 2024 (Anticipated)
Study Completion Date
June 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
The primary purpose of this study is to compare balloon Eustachian tuboplasty (BET) combined with tympanostomy tube insertion and simply tympanostomy tube insertion in the treatment of otitis media with effusion (OME) in post-radiotherapy patients on the improvement of subjective symptoms (ear fullness, etc.) and the tympanogram. The secondary purpose is to clarify the effects of BET on the incidence of middle ear infection and slippage of ventilation tube during tube retention, as well as to determine the difference of hearing improvement between the two management methods.
Detailed Description
Nasopharyngeal carcinoma (NPC) is the most common malignancy of the nasopharynx, of which Guangdong Province is the high-risk area. At present, the comprehensive treatment plan based on radiotherapy (RT) makes NPC a good prognosis, so it is the complications of RT that have become the main factor affecting the life quality of patients. Otitis media with effusion (OME) following RT is the most common ear complication, which is characterized by a large amount of effusion from the tympanic cavity (the cavity of middle ear). Ear fullness and hearing loss could take place because of tympanic effusions, reducing the patient's ability to communicate and increasing life risk. Currently Eustachian tube dysfunction (ETD) due to RT is regarded as an important causative factor. The Eustachian tube, connecting the middle ear to the outside world, is an important ventilation pipe. RT could lead to hyperemia, edema, and then fibrosis and atrophy of the Eustachian tube mucosa, resulting in organic changes of the Eustachian tube, including stiffness, adhesions, narrowing and even atresia, and eventually the formation of OME. Comparatively, non-radiation-related OME is usually a nonorganic disease, which is the biggest pathogenic difference between the two. However, treatment of OME following RT is still the same as that of non-radiation-related one, but the clinical efficacy is much worse than the latter. Conservative treatments such as physical and pharmacological therapy usually turn out to be ineffective. The most widely used ones are tympanocentesis and tympanostomy tube insertion. Tympanocentesis is to directly pierce the tympanic membrane and drain the middle ear effusion. However, the drainage port usually heals within 3-5 days, so it is often necessary to pierce repeatedly. The ventilation tube insertion is considered to achieve continuous drainage, but the risks of middle ear infection, slippage of ventilation tube, and permanent tympanic membrane perforation is high after the placement of tube. Therefore, the residence time of the ventilation tube is generally no more than 6-9 months. At present, the treatments of OME following RT just deal with symptoms, instead of the cause--ETD, resulting in low cure rate, high recurrence rate and high complication rate. In recent years, balloon Eustachian tuboplasty (BET) has been performed successfully with encouraging results in patients with ETD by dilating (make larger) the cartilage segment of the Eustachian tube. However, ETD following RT used to be recognized as a contraindication to BET, possibly due to more complex pathogenesis, scruples for damage to the internal carotid artery in the lateral of the Eustachian tube, and Eustachian tube atresia. The above reasons are only speculation, and there have been already a few reports of BET being used in OME after RT for head and neck tumors. The primary purpose of this study is to compare BET combined with tympanostomy tube insertion and simply tympanostomy tube insertion in the treatment of OME in post-radiotherapy patients on the improvement of subjective symptoms (ear fullness, etc.) and the tympanogram. The secondary purpose is to clarify the effects of BET on the incidence of middle ear infection and slippage of ventilation tube during tube retention, as well as to determine the difference of hearing improvement between the two management methods.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Otitis Media With Effusion After Nasopharyngeal Carcinoma
Keywords
Balloon Eustachian Tuboplasty, Tympanostomy Tube Insertion, Otitis Media With Effusion, Nasopharyngeal Carcinoma

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
208 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Balloon Eustachian Tuboplasty with Tympanostomy Tube Insertion
Arm Type
Experimental
Arm Title
Tympanostomy Tube Insertion
Arm Type
Other
Intervention Type
Procedure
Intervention Name(s)
Balloon Eustachian Tuboplasty with Tympanostomy Tube Insertion
Intervention Description
Under local or general anesthesia, insert a balloon into one Eaustachian tube and inflate it for up to two minutes. The balloon is then removed. Subsequently, pierce the tympanic membrane in the front and lower quadrants, suck the tympanic effusion, and then insert a tympanic ventilation tube. The tube will be removed 6 months later.
Intervention Type
Procedure
Intervention Name(s)
Tympanostomy Tube Insertion
Intervention Description
Under local or general anesthesia, pierce the tympanic membrane in the front and lower quadrants, suck the tympanic effusion, and then insert a tympanic ventilation tube. The tube will be removed 6 months later.
Primary Outcome Measure Information:
Title
changes in air pressure (Tympanogram)
Description
Tympanogram, which measures the movement of the tympanic membrane in response to changes in air pressure, is classified by types - Type A, B and C. Each classification indicates a range that falls between normal and abnormal.
Time Frame
collected at 1 month, 3 months, 6 months and 12 months after the ventilation tube removal
Secondary Outcome Measure Information:
Title
Incidence of Otitis Media
Description
The number of days of ear discharges or otorrhoea in a 6-month period of tube retention
Time Frame
6 months post-operatively during tube retention
Title
Incidence of Slippage of Ventilation Tube
Description
The number of times the ventilation tube falls off in a 6-month period of tube retention
Time Frame
6 months post-operatively during tube retention
Title
Eustachian Tube Dysfunction Questionnaire (ETDQ-7)
Description
The ETDQ-7 tool is used to assess the symptoms of Otitis Media With Effusion (OME), which consists of seven items with a scale of graduated responses ranging from 1 (No Problem) to 7 (Severe Problem), and 4 would correspond to a Moderate Problem. If the total score is more than 14, it is considered that there is eustachian tube dysfunction. The average post-operative ETDQ-7 score is less than 2.1 or decrease > 0.5 (minimal clinically important difference=0.5), it is considered that the eustachian tube function is improved.
Time Frame
collected at 1 month, 3 months, 6 months and 12 months after the ventilation tube removal
Title
Hearing gap
Description
It is the change of air-bone conduction difference between pre-operation and post-operation, which is measured by Pure-Tone Audiometry.
Time Frame
collected at 1 month, 3 months, 6 months and 12 months after the ventilation tube removal

10. Eligibility

Sex
All
Minimum Age & Unit of Time
15 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: patients clinically diagnosed OME after radiotherapy for NPC (diagnostic criteria: have fluid drained from tympanic cavity during tympanocentesis) , who had completed radiotherapy for ≥6 months, and had failed to respond after two or more times of tympanocentesis Eustachian Tube Dysfunction Questionnaire score greater than 14 clinical findings of a retracted drum fluid behind the drum tympanometry type B or C results patients volunteered to participate in the study and signed the informed consent patients volunteered to bear the corresponding costs of surgery and consumables. Exclusion Criteria: NPC recurrence or other malignant tumor after radiotherapy a perforated tympanic membrane the presence of a ventilation tube a period of less than six months following the final radiotherapy treatment clear diagnosis of Eustachian ostium atresia or nasal obstruction diseases, such as severe deviated nasal septum, nasal polyp, choanal atresia, osteoradionecrosis of skull base after radiotherapy, etc. patients with severe underlying diseases could not tolerate general anesthesia patients who could not cooperate (including poor hearing and radiation encephalopathy) patients with other middle ear diseases, such as middle ear cholesteatoma, osteoradionecrosis of temporal bone after radiotherapy, etc. severe deglutition disorders cleft palate
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Hao Xiong
Phone
+8613725130384
Email
xiongh7@mail.sysu.edu.cn
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hao Xiong
Organizational Affiliation
Sun Yat-sen Memorial Hospital,Sun Yat-sen University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sun Yat-sen Memorial Hospital, Sun Yat-sen University
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510120
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hao Xiong
Phone
+8613725130384
Email
xiongh7@mail.sysu.edu.cn

12. IPD Sharing Statement

Plan to Share IPD
Yes

Learn more about this trial

A Prospective, Randomized, Controlled Clinical Study of BET Combined With Tympanostomy Tube Insertion in the Treatment of Intractable OME After Radiotherapy for NPC

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