Hearing Loss and Osteoporosis

NCT ID: NCT03895333

Last Updated: 2020-04-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

160 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-03-01

Study Completion Date

2020-03-01

Brief Summary

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To compare the audiological profiles in postmenopausal women with and without osteoporosis and to examine the pattern of hearing loss in osteoporotic patients. postmenopausal women will be separated as normal, osteopenic and osteoporotic according to bone mineral densitometry results. The evaluation of hearing test will be done in these groups and the results will be compared between the groups.

Detailed Description

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Conditions

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Hearing Loss Osteoporosis, Postmenopausal

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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study group

women with hearing loss and osteoporosis will develop the study group.

Audiological profiling and bone mineral densitometry measurement

Intervention Type OTHER

bone mineral densitometry measurements and hearing test patients, osteoporosis according to whether the hearing test will be analyzed.

control group

women who have hearing loss but have no osteoporosis will constitute the control group.

Audiological profiling and bone mineral densitometry measurement

Intervention Type OTHER

bone mineral densitometry measurements and hearing test patients, osteoporosis according to whether the hearing test will be analyzed.

Interventions

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Audiological profiling and bone mineral densitometry measurement

bone mineral densitometry measurements and hearing test patients, osteoporosis according to whether the hearing test will be analyzed.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Between 45-60 years
* postmenopausal women

Exclusion Criteria

* Women over 60 years old,
* acute or chronic otitis media,
* ear surgery,
* use of ototoxic drugs,
* congenital hearing loss,
* previous long-term steroid use,
* malignant or benign neoplasm of the brain,
* Patients with a history of exposure to noise were excluded from the study.
Minimum Eligible Age

45 Years

Maximum Eligible Age

60 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Kanuni Sultan Suleyman Training and Research Hospital

OTHER

Sponsor Role lead

Responsible Party

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Pınar Kadirogulları

Principal investigator, M.D, Department of Obstetrics and GynecologyR

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Kanuni Sultan Süleyman Training and Research Hospital

Istanbul, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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2019.01.01

Identifier Type: -

Identifier Source: org_study_id

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