Correlation analysis between transcutaneous electrical stimulation and abdominal symptoms
Not Applicable
Recruiting
- Conditions
- constipation
- Registration Number
- JPRN-UMIN000051103
- Lead Sponsor
- Juntendo University School of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Not provided
Exclusion Criteria
1. Patients with organic constipation 2. Patients with a history of intestinal resection 3. Patients using medical electrical equipment 4. Patients who are pregnant or have just given birth 5. Those who started using new products such as food/beverages, supplements and drugs for constipation within 2 weeks from the start of electrical stimulation
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method