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Clinical Trials/KCT0009275
KCT0009275
Not yet recruiting
未知

A clinical research on the brain-body physiological signal measurements of functional dyspepsia patients to develop prediction algorithm for pattern identification

Kyung Hee University Oriental Medicine Hospital at Gangdong0 sites100 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Diseases of the digestive system
Sponsor
Kyung Hee University Oriental Medicine Hospital at Gangdong
Enrollment
100
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational Study
Sex
All

Investigators

Sponsor
Kyung Hee University Oriental Medicine Hospital at Gangdong

Eligibility Criteria

Inclusion Criteria

  • Adult men and women aged 19 to 65

Exclusion Criteria

  • (1\) Individuals diagnosed with organic gastrointestinal disorders such as ulcers, cancer, or inflammatory bowel diseases through gastrointestinal endoscopy within the past 3 years prior to screening.
  • (2\) Individuals exhibiting alarm symptoms such as severe weight loss, bloody stools, dysphagia, persistent vomiting, or abdominal pain.
  • (3\) Individuals with significant neurological or psychiatric medical history such as major depressive disorder, anxiety disorder, schizophrenia, or those currently suffering from such conditions.
  • (4\) Individuals with serious organic conditions affecting physiological signals (e.g., congestive heart failure, angina, myocardial infarction, arrhythmias, valvular disease).
  • (5\) Individuals who have taken medications (e.g., anticoagulants, vasodilators, antihypertensives) that may affect physiological signals on the day of physiological signal measurement.
  • (6\) Individuals with conditions such as defects in the measurement site (forehead, finger, wrist, chest), skin diseases, or other factors making it difficult to measure physiological signals.
  • (7\) Individuals who have undergone gastrointestinal surgery within the past 6 months.
  • (8\) Pregnant women.
  • (9\) Students, researchers, or staff affiliated with the laboratory conducting the study, including undergraduate and graduate students.
  • (10\) Individuals deemed unsuitable for participation in the study by the principal investigator or study coordinator for any other reason.

Outcomes

Primary Outcomes

Not specified

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