Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 10:52 PM
Ignite Modification Date:
2025-12-24 @ 10:52 PM
NCT ID:
NCT00856869
Eligibility Criteria:
Inclusion Criteria:
General - all subjects
1. Males or females (females of non-childbearing potential or of childbearing potential while taking medically appropriate contraception)
2. Caucasian
3. BMI: between 19 and 34 kg.m-2
4. BW: between 45 and 110 kg
5. willing and able to provide informed consent Healthy volunteers (group N)
6. Age: 18 - 40 years (inclusive) e.g. \> 60 years
7. Assessed as healthy based on the pre study examination Hepatic cirrhosis
8. Age: 18 - 75 years
9. stable compensated liver cirrhosis (cryptogenic, posthepatic, alcoholic) with histo-logical or macroscopic (e.g. laparascopy, biopsy, ultrasound sonography or other adequate imaging techniques) confirmation Nonalcoholic steatohepatitis (NASH)
10. Age: 18 - 75 years
11. Diagnosis of NASH confirmed by liver biopsy
Exclusion Criteria:
General - all subjects
1. Previous participation in the trial
2. Participant in any other trial during the last 90 days
3. Donation of blood during the last 60 days or a history of blood loss exceeding 450 mL within the last 3 months
4. History of any clinically relevant allergy
5. Uncontrolled diabetes mellitus or any further intolerability of the Galactose test
6. Presence of acute or chronic infection
7. Resting systolic blood pressure \> 160 or \< 90 mmHg, diastolic blood pressure \> 95 or \< 50 mmHg
8. Clinically relevant ECG-abnormalities, prolonged QTc with \> 450 msec in males and \> 460 msec in females in particular
9. Clinically relevant ECG-abnormalities that constitute a contraindication for the Lido-cain-MEG'-X-test
10. Positive HIV test
11. Positive alcohol or urine drug test on recruitment
12. Daily use of \> 30 gr alcohol
13. Smoking more than 15 cigarettes/day or equivalent of other tobacco products
14. Use of prohibited medication
15. Suspicion or evidence that the subject is not trustworthy and reliable
16. Suspicion or evidence that the subject is not able to make a free consent or to under-stand the information in this regard
General - all females
17. Positive pregnancy test
18. Lactating
19. Not using appropriate contraception in premenopausal women All healthy subjects
20. Presence or history of any relevant comorbidity (list of past and present diseases will be reviewed by an expert panel)
21. Presence of any relevant abnormality in the laboratory safety tests, especially low haemoglobin, increased liver enzymes, reduced serum creatinine (laboratory test abnormalities will be reviewed by an expert panel)
22. Positive serology for HBsAg, anti HBc and anti HCV
23. History of alcohol and/or drug abuse.
Patients with hepatic disease
24. Biliary liver cirrhosis
25. Liver impairment due to space-occupying processes (e.g. carcinoma)
26. State after liver transplantation or patient scheduled for liver transplantation
27. Fluctuating or rapidly deteriorating hepatic function
28. Significant bleeding diathesis
29. Oesophageal bleeding within the last 8 weeks before study entry
30. Ascites \> 6 L on abdominal US
31. Number Connection test: time to connect 25 consecutive numbers \> 30 sec
32. Presence or history of any relevant comorbidity other than hepatic disease (list of past and present diseases will be reviewed by an expert panel)
33. Clinically relevant abnormal laboratory values other than those associated or sufficiently explained by the existing liver disease (laboratory test abnormalities will be reviewed by an expert panel)
34. History of drug or alcohol abuse within 2 months prior to dosing
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
75 Years
Study:
NCT00856869
Study Brief:
Protocol Section:
NCT00856869