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Clinical study on acupuncture treatment of spleen stomach weakness type tinnitus guided by the theory of brain gut axis

Clinical study on acupuncture treatment of spleen stomach weakness type tinnitus guided by the theory of brain gut axis

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2024000643
Enrollment
Unknown
Registered
2024-11-03
Start date
2024-10-08
Completion date
Unknown
Last updated
2024-11-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

tinnitus

Interventions

Experimental group:Acupuncture+ICBT
Control group:Fake acupuncture +ICBT

Sponsors

Chongqing Three Gorges Medical College
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria of traditional Chinese and Western medicine for primary tinnitus and the syndrome type is spleen and stomach weakness type; 2. Age range between 18 and 80 years old (including 18 and 80 years old); 3 pairs of tolerants in this experiment; 4. Those who have not received other treatments at the same time; 5.Voluntary signatories of informed consent form; 6.People is within the scope of applicability of the technology used in this study. Anyone who meets the above six conditions is eligible to participate in this study.

Exclusion criteria

Exclusion criteria: 1. Patients who have experienced new cardiovascular and cerebrovascular diseases or sudden hearing loss in the past three months; 2 Patients with a history of massive cerebral infarction severe endocrine system disease severe infectious diseases and toxic encephalopathy; 3. There is a history of dizziness with acupuncture and contraindications for acupuncture treatment include skin damage infection and other conditions that are not suitable for acupuncture treatment; 4. Consciously or mentally impaired unable to cooperate with the researcher to complete the study; 5. Women with acute abdomen pregnancy and lactation; 6. History of head and neck injuries and history of taking special medications; 7. Within the past three months the patient has undergone or is currently participating in other clinical trials;

Design outcomes

Primary

MeasureTime frame
SDS;5-HT;SF-36;PTA;THI;Tinnitus matching;PSQI;

Secondary

MeasureTime frame
GABA;SAS;5-HT;

Countries

China

Contacts

Public ContactJiao Liang

Chongqing Three Gorges Medical College

20230028@cqtgmc.edu.cn15171917880

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026