Effect of Hyperbaric Oxygen Therapy(HBOT) on Patients With Sudden Sensorineural Hearing Loss(SSNHL) and Coagulation Function

NCT ID: NCT06819202

Last Updated: 2025-05-14

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

NOT_YET_RECRUITING

Total Enrollment

1309 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-06-01

Study Completion Date

2025-12-01

Brief Summary

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The objective of this observational study was to understand the effect of HBO on patients with SSNHL and its association with coagulation function and prognosis.

The main question it aims to answer is whether HBO therapy can improve outcomes and coagulation function in patients with SSNHL.

The prognosis of SSNHL patients receiving HBO and SSNHL patients not receiving HBO were compared

Detailed Description

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Conditions

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Sudden Sensorineural Hearing Loss (SSNHL) Hyperbaric Oxygen Therapy

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Interventions

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Hyperbaric oxygen treatment

HBO therapy is the process of inhaling 100% pure oxygen in an environment above one atmosphere (pressure range: 2.0-3.0 absolute atmospheres) to treat a disease.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Meet the diagnostic criteria for sudden deafness in the American Academy of Otolaryngology Head and Neck Surgery 2019 Clinical Practice Guidelines for Sudden Deafness;
* Aged 18-75 years old;
* Patients with unilateral sudden deafness for the first time, and the onset time is less than 2 weeks.

Exclusion Criteria

* Patients with other ear diseases, such as auditory trauma, barotrauma, retrocochlear disease, bilateral hearing loss, history of chronic otitis media in the same ear, and history of surgery in the same ear;
* Patients with serious primary diseases such as heart, liver, kidney dysfunction and hematopoietic system diseases;
* Pregnant and nursing patients;
* Accompanied by serious mental illness;
* Patients with incomplete clinical data.
Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Sun Yuting

OTHER

Sponsor Role lead

Responsible Party

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Sun Yuting

PhD student

Responsibility Role SPONSOR_INVESTIGATOR

Locations

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Shanghai University of Traditional Chinese Medicine

Shanghai, Putuo, China

Site Status

Countries

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China

Central Contacts

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Sun Yuting

Role: CONTACT

+89 198 2175 8594

Facility Contacts

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Sun YT Sun, PhD student

Role: primary

19821758594

Other Identifiers

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PTEC-A-2025-1(S)-1

Identifier Type: -

Identifier Source: org_study_id

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