DRKS00016795Completed未知
Perioperative assessment of the remnant liver functional capacity with the 13C methacetin breath test - ReLiF study
Allgemein- und Viszeralchirurgie Asklepios Klinik Barmbek0 sites30 target enrollmentStarted: February 21, 2019Last updated:
Conditions
Trial Snapshot
- Phase
- 未知
- Status
- Completed
- Sponsor
- Enrollment
- 30
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
- Allocation
- N/a: Single Arm Study
- Masking
- Blinded (masking used)
Eligibility Criteria
- Ages
- 18 Years to one (—)
- Sex
- All
Inclusion Criteria
- •All adult patients (> 18 years of age) able to give consent, who will undergo a liver resection of 3 or more liver segments according to Couinaud classification at the Department of General and Visceral Surgery of the Asklepios Klinik Barmbek within one year of the study beginning.
Exclusion Criteria
- •1. Patients with an allergy to acetaminophen or methacetin.
- •2. Patients who have received a strong CYP1A2 agonist (e.g., ciprofloxacin, fluvoxamine, enoxacin, verapamil) within the half-life of these substances
Investigators
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