None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Adults aged 19 to 65 years 2. Individuals who meet the Rome IV diagnostic criteria for functional constipation 3. Individuals who meet the above criteria, have received a detailed explanation of this clinical study, fully understood it, voluntarily decided to participate, and provided written informed consent to comply with study requirements
Exclusion criteria
Exclusion criteria: 1. Individuals who do not meet the age criteria (19–65 years) 2. Individuals who have undergone gastrointestinal surgery within the past 6 months 3. Individuals with gastrointestinal bleeding, obstructive lesions, or open abdominal wounds 4. Individuals with a history of severe respiratory, cardiovascular, renal, gastrointestinal, hepatic, endocrine, hematologic, neurological (including motor disorders), psychiatric disease, or other chronic conditions, as well as alcohol or drug dependence 5. Individuals who have participated in another clinical trial of an investigational drug or marketed product within 60 days prior to study initiation 6. Individuals with a history of significant adverse reactions such as hypersensitivity to investigational drugs 7. Women who are pregnant or breastfeeding
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| Serum concentrations of Aspartate Transaminase (AST);Serum concentrations of Alanine Transaminase (ALT);Serum concentrations of Alkaline Phosphatase (ALP);Serum concentrations of Blood Urea Nitrogen;Serum concentrations of Creatinine | — |
Primary
| Measure | Time frame |
|---|---|
| Serum concentrations of delta-9 Tetrahydrocannabinol (THC);Serum concentrations of Cannabidiol (CBD) | — |
Countries
Korea, Republic of
Contacts
Wonkwang University