The Clinical Research of Auricular Magnet for Anorexia in Children
NCT ID: NCT06619548
Last Updated: 2024-10-01
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
RECRUITING
NA
144 participants
INTERVENTIONAL
2024-10-31
2025-07-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
POTS-CFS Study: Orthostatic Intolerance in the Context of Pediatric ME/CFS
NCT06054958
Pilot Testing of Food Images in Children
NCT03338634
Multicenter Trial of Magnetic Mini-Mover for Pectus Excavatum
NCT01327274
Comparison of Antibiotic Therapy Alone or Combined With Corticosteroids for the Treatment of Nontuberculous Mycobacterial Cervicofacial Lymphadenitis in Children: A Randomized Double-Blind Placebo-Controlled Study
NCT01614977
Absorption of Corticosteroids in Children With Juvenile Dermatomyositis
NCT00004357
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
CROSSOVER
TREATMENT
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Group A
The participants will have auricular magnets with a strength of 1800 Gauss applied to specific acupoints in the first treatment phase. This is followed by a 14-day washout period. In the second treatment phase, the participants will have auricular magnets with no magnetic strength applied to the same acupoints.
Auricular magnet with a magnetic strength of 1800 Gauss
Auricular magnets with a magnetic strength of 1800 Gauss are used as the experimental group.
Auricular magnet with no magnetic strength
Auricular magnets with no magnetic strength are used as placebo control.
Group B
The participants will have auricular magnets with no magnetic strength applied to specific acupoints in the first treatment phase. This is followed by a 14-day washout period. In the second treatment phase, the participants will have auricular magnets with a strength of 1800 Gauss applied to the same acupoints.
Auricular magnet with a magnetic strength of 1800 Gauss
Auricular magnets with a magnetic strength of 1800 Gauss are used as the experimental group.
Auricular magnet with no magnetic strength
Auricular magnets with no magnetic strength are used as placebo control.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Auricular magnet with a magnetic strength of 1800 Gauss
Auricular magnets with a magnetic strength of 1800 Gauss are used as the experimental group.
Auricular magnet with no magnetic strength
Auricular magnets with no magnetic strength are used as placebo control.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
1. Postprandial fullness
2. Early satiety
3. Epigastric pain
4. Epigastric burning sensation or has a weight below the 15th percentile for age and sex for at least two months.
2. No prokinetic or appetite-stimulating Western medications or spleen and stomach-strengthening Chinese medications have been used within the past two weeks.
Exclusion Criteria
2 Years
6 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
China Medical University Hospital
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Hung-Rong Yen
Director of the Department of Integration of Traditional Chinese-Western Medicine
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Hung-Rong Yen, M.D., Ph.D.
Role: STUDY_CHAIR
China Medical University, China
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
China Medical University Hospital
Taichung, , Taiwan
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
CMUH112-REC1-108
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.