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Feasibility of quantitative measurement of several components in abdominal examination for functional dyspepsia

Feasibility of quantitative measurement of several components in abdominal examination for functional dyspepsia

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0003369
Enrollment
120
Registered
2018-11-23
Start date
2018-07-20
Completion date
Unknown
Last updated
2019-03-11

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

Conditions

None listed

Interventions

None listed

Sponsors

Korea Institute of Oriental Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patient inclusion criteria 1) Subjects between the ages of 20 and 65 years; 2) Subjects who meet functional dyspepsia (FD) definition of Rome ? criteria and have undergone the above symptoms for a minimum of three months from at least six months ago to the present time. 2. Control inclusion criteria 1) Subjects who have no problem communication; 2) Subjects who check less than 20 mm visual analogue scale for dyspeptic symptoms; 3) Subjects who have not gastrointestinal disorder and symptoms; 4) Subjects who have not serious structural diseases (disease of liver, heart, lung, or kidney);

Exclusion criteria

Exclusion criteria: 1) Subjects who have organic disease such as peptic ulcer or gastroesophageal reflux disease go through esophagogastroduodenoscopy and laboratory test; 2) Subjects who have obvious signs of irritable bowel syndrome (IBS); 3) Subjects who have alarm symptoms (e.g., weight loss, black or tar stool, or dysphagia); 4) Subjects who have serious structural disease (e.g., disease of heart, lung, liver or kidney) or mental illness; 5) Subjects who have had surgery related with the gastrointestinal tract, except for appendectomy more than six months ago; 6) Subjects who are pregnant or breastfeeding; 7) Subjects who have taken any other clinical trial within 1 months; 8) Subjects who are human immunodeficiency virus (HIV) positive; 9) Subjects who have difficulty in attending the trial (e.g., paralysis, severe mental or psychological abnormality, dementia, drug addiction, time constraint, severe disorder in vision or hearing, outpatient treatment impossibility, illiteracy).

Design outcomes

Primary

MeasureTime frame
Costal angle (sterno-costal angle)

Secondary

MeasureTime frame
Abdominal sound evaluated by stethoscope;Abominal diagnosis by Korean medicine doctor;Questionnare of patter identification for functional dyspepsia;Damum questionnaire;Food retention questionnaire;Spleen qi deficiency questionnaire;Scale for stomach qi deficiency pattern;Cold-heat questionnaire;Deficiency-excess questionnaire;Nepean dyspepsia index - Korean version;Abdominal wall thickness evaluated by sonography;Gastric emptying test using ultrasonography;Pressure depth evaluated by algometer

Countries

Korea, Republic of

Contacts

Public ContactJae-Woo Park

Kyung Hee University Oriental Medicine Hospital at Gangdong

pjw2907@hanmail.net+82-2-440-7131

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Jul 15, 2026