DRKS00033099CompletedUnknown
Absorption of X-Pro-Dipeptides following Oral Ingestion - X-PRO
Institut für Pharmakologie, Universitätsmedizin Greifswald0 sites9 target enrollmentStarted: November 24, 2023Last updated:
Conditions
Trial Snapshot
- Phase
- Unknown
- Status
- Completed
- Sponsor
- Enrollment
- 9
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
- Allocation
- N/a: Single Arm Study
- Masking
- Open (masking not used)
Eligibility Criteria
- Ages
- 18 Years to 40 Years (—)
- Sex
- All
Inclusion Criteria
- •understands the study purpose and design
- •- contractually capable and provides signed informed consent form
- •- healthy condition or mild and/or well treated forms of allergies, asthma,
- •hypertension, and orthopedic diseases
- •- a maximum of 2 chronically taken drugs
Exclusion Criteria
- •a.BMI > 35 kg/m2 and <18 kg/m2
- •b.known pregnancy or lactation period
- •c.women: positive urine pregnancy test at screening or pharmacokinetic
- •d.anemia (hemoglobin < 13 g/dl (8,07 mmol/l) in men or < 12 g/dl (7,45
- •mmol/l) in women
- •e.blood donation within the last 4 weeks
- •f.elevated liver function tests (ALAT, ASAT, yGT, Bilirubin > 2x ULN)
- •g.reduced renal function (eGFRMDRD < 60 ml/min/1,7m2)
- •h.known history of coeliac disease or gluten intolerance
- •i.psychiatric disease or drug dependency
- •j.use of recreational drugs more than twice a week
- •k.poor venous conditions that make it impossible to place a peripheral
- •venous catheter and regularly draw blood through it
Investigators
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