Repair of Tympanic Membrane Perforation Using Tachosil Under Local Anesthesia
Primary Purpose
Tympanic Membrane Perforation
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Tachosil
fascia and cartilage
Sponsored by
About this trial
This is an interventional treatment trial for Tympanic Membrane Perforation focused on measuring tympanic membrane perforation, tachosil, local anesthesia
Eligibility Criteria
Inclusion Criteria:
- chronic tympanic membrane perforation
- dry ear at least 4 weeks before the procedure
- no evidence of cholesteatoma
- hearing test in the last 3 months
- signing informed consent
Exclusion Criteria:
- age under 18 years
- pregnant
- breastfeeding
- a known sensitivity for any ingredient
- a perforation that is more than one third of the tympanic membrane area.
- new onset perforation (less than 3 months)
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
tympanoplasty using fascia and cartilage
Tachosil
Arm Description
tympanoplasty under general anesthesia using fascia and cartilage witch is the gold standard for treating tympanic membrane perforations.
repair of tympanic perforations under local anesthesia using Tachosil patch.
Outcomes
Primary Outcome Measures
closure of tympanic membrane perforation
one month post operative the patient will be re-examined in the clinic to see if the perforation is closed.
Secondary Outcome Measures
Full Information
NCT ID
NCT04428463
First Posted
June 9, 2020
Last Updated
June 11, 2020
Sponsor
HaEmek Medical Center, Israel
1. Study Identification
Unique Protocol Identification Number
NCT04428463
Brief Title
Repair of Tympanic Membrane Perforation Using Tachosil Under Local Anesthesia
Official Title
Fibrinogen- Based Collagen Fleece Graft Myringoplasty for Chronic Tympanic Membrane Perforations - a Prospective Study
Study Type
Interventional
2. Study Status
Record Verification Date
June 2020
Overall Recruitment Status
Unknown status
Study Start Date
June 30, 2020 (Anticipated)
Primary Completion Date
June 2021 (Anticipated)
Study Completion Date
June 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
HaEmek Medical Center, Israel
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Tympanic membrane perforations are common medical problem that encounters a lot of patients in all age groups.
The gold standard for treatment of perforations is tympanic membrane closure procedure (tympanoplasty) which is done under general anesthesia.
This procedure could be problematic for many patients who are not suitable for general anesthesia due to their medical status.
It's also time consuming for the patient and for the medical system, since it takes a lot of time to reach the operation room and hospitalization for at least two days.
The purpose in this study is to use Tachosil (Fibrinogen based patch) under local anesthesia to close tympanic membrane perforations.
Tachosil is in use for hemostasis and for tissue repair after injury. Tachosil is bound to the tissue and form a waterproof membrane. In the setting of ENT clinic and under local anesthesia, the investigators will start the procedure with debridement of the tympanic perforation edges, then they will close the perforation using two pieces of Tachosil under and above the perforation in the right form (active side to the active side).
If the results will be similar to tympanoplasty results, this method may be used for closure of tympanic perforation and save time and money for the patient and for the health system.
Detailed Description
Tympanoplasty is the gold standard treatment for tympanic membrane perforation.
It is done under general anesthesia in the following form:
Incision in the post auricular area, harvesting of fascia and cartilage from the concha of the pinna .
In Trans ear canal approach starting with debridement of the edges of the tympanic membrane perforation and closing the perforation using cartilage and fascia.
After being informed about the study and potential risks, all patients giving informed consent will participate in the study.
This study will include two groups. The first group will be treated with the conventional way as described above. The interventional group will be treated using Tachosil in the following order:
Local anesthesia using Lidocadren (lidocaine and epinephrine) will be injected to the ear canal using dental needle.
Debridement of the edges of the tympanic membrane perforation Placing the tachosil under and above the perforation in the correct order. The patient could be discharged home immediately after the procedure if no adverse effects are seen (dizziness, nausea or vomiting).
After one month, similar to the conventional treatment method, the patient will be invited to the otology clinic, for hearing test and microscopic examuntaion of the tympanic membrane, to see if the perforation is closed.
The study will compare the success rate in the two groups and if it will be similar that will help publish this method and use it in patients who are not suitable to general anesthesia and in hospitals were waiting time table for operation room is very long.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tympanic Membrane Perforation
Keywords
tympanic membrane perforation, tachosil, local anesthesia
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
two groups. In one we will use the conventional treatment strategy using tympanoplasty with fascia and cartilage.
in the intervention group we will use tachosil in closing the perforations.
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
27 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
tympanoplasty using fascia and cartilage
Arm Type
Active Comparator
Arm Description
tympanoplasty under general anesthesia using fascia and cartilage witch is the gold standard for treating tympanic membrane perforations.
Arm Title
Tachosil
Arm Type
Experimental
Arm Description
repair of tympanic perforations under local anesthesia using Tachosil patch.
Intervention Type
Procedure
Intervention Name(s)
Tachosil
Intervention Description
tympanic membrane perforation repair using Tachosil patch under local anesthesia
Intervention Type
Procedure
Intervention Name(s)
fascia and cartilage
Intervention Description
tympanic membrane perforation repair using fascia and cartilage under general anesthesia
Primary Outcome Measure Information:
Title
closure of tympanic membrane perforation
Description
one month post operative the patient will be re-examined in the clinic to see if the perforation is closed.
Time Frame
one month after the procedure
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
chronic tympanic membrane perforation
dry ear at least 4 weeks before the procedure
no evidence of cholesteatoma
hearing test in the last 3 months
signing informed consent
Exclusion Criteria:
age under 18 years
pregnant
breastfeeding
a known sensitivity for any ingredient
a perforation that is more than one third of the tympanic membrane area.
new onset perforation (less than 3 months)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
lev shlizerman, md
Phone
00972504433469
Email
lev_sh@clalit.org.il
First Name & Middle Initial & Last Name or Official Title & Degree
mary ghrayeb haddad, md
Phone
00972509311771
Email
mary_gh@clalit.org.il
12. IPD Sharing Statement
Learn more about this trial
Repair of Tympanic Membrane Perforation Using Tachosil Under Local Anesthesia
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