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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04366674
Other study ID # S-K1145
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 1, 2013
Est. completion date June 30, 2019

Study information

Verified date April 2020
Source Peking Union Medical College Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

to study the benefical audiological and/or otological effect by mordified restoration of tensor veli palatini in cleft palate repair compared to traditional Langenbeck's repair and merely levator veli palatini restoration.


Description:

71 patients with cleft palate received surgery were divided into 3 groups. Group 1: patients who received Langenbeck surgery without specific restoration of levator veli palatini or tensor veli palatini. Group 2: patients who received palate surgery with special levator veli palatini restoration. Group 3: patients who received palate surgery with modified tensor veli palatini restoration. The conductive auditory brainstem response and 226 Hz tympanometry were used to test the audiological and otological status of the three groups. Preoperative and postoperative results were compared intragroup and intergroup.


Recruitment information / eligibility

Status Completed
Enrollment 71
Est. completion date June 30, 2019
Est. primary completion date January 31, 2019
Accepts healthy volunteers No
Gender All
Age group 6 Months to 60 Months
Eligibility Inclusion Criteria:

- Clinical diagnosis of cleft palate.

- Primary palate repair.

Exclusion Criteria:

- Severe general disease

- Confirmed hereditary hearing loss or neuropathic hearing loss.

- Received any kind of audiological or otological therapy before.

- Patients and/or his/her don't want to continue the clinical trial.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
cleft palate repair
restoration of tensor veli palatini for the purpose of the muscle function recovery.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Peking Union Medical College Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary Hearing level Auditory brainstem response was tested in all three groups after surgery. The air conductive hearing threshold was used to assess the hearing level. 3 months after surgery
Primary The otological status of middle ear 226 tympanometry was tested in all three groups after surgery. The results of 226 Hz tympanometry were classified based on Liden/Jerger classification. Four classes of tympanometry results were included. 3 months after surgery
Primary Hearing level Auditory brainstem response was tested in all three groups before surgery. The air conductive hearing threshold was used to assess the hearing level. 0 to 3 months before surgery
Primary The otological status of middle ear 226 tympanometry was tested in all three groups before surgery. The results of 226 Hz tympanometry were classified based on Liden/Jerger classification. Four classes of tympanometry results were included. 0 to 3 months before surgery
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