EUROPAC-2 - Pain Treatment of Hereditary and Idiopathic Pancreatitis
CompletedPhase 3NCT00142233
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This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
This is a multi-centre randomised phase III, double blind, placebo controlled, parallel group, outpatient study in patients diagnosed with hereditary pancreatitis and idiopathic chronic pancreatitis. The hypothesis to be tested is a 30% reduction in the number of days due to pancreatitis from 12.5 days per year to less than nine days per year under the treatment with magnesium or an antioxidant cocktail called ANTOX. A total of 288 patients will be randomised to one of three treatment groups in order to compare pancreatic pain over a twelve month period.
Study details
- Official title
- Double Blind Randomised Controlled Trial to Investigate the Efficacy of ANTOX (Vers) 1.2 and MGCT (Magnesiocard) for the Treatment of Hereditary Pancreatitis and Idiopathic Chronic Pancreatitis
- Conditions
- Pancreatitis
- Interventions
- Dietary supplement: ANTOX (vers.)1.2
- Drug: Magnesium
- Other: Placebo ANTOX (vers)1.2
- Other: Placebo Magnesiocard (2.5 mmol)
- Sponsor
- University Medicine Greifswald
- Start date
- 2005-06-06
- Primary completion
- 2019-09
- Sex
- All
- Age range
- from 5 Years to 75 Years
- Results posted
- No results posted in this snapshot
- Total sites listed
- 0
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: 1. Patients must have had symptoms of pancreatitis for at least one year. 2. Patients must be willing to be followed up regularly for at least one year. 3. Patients aged 5 to 75 years of age. 4. Individuals must have characteristic pancreatic pain that is either intermittent or continuous (2 or more episodes during the last 12 months) 5. Patients with documented Hereditary Pancreatitis (HP), clinically defined or proven by gene mutations in the PRSS1 Gene, or patients with Idiopathic Chronic Pancreatitis (ICP) and no mutations detected in the PRSS1 gene. This may include patients with a history of alcohol intake who have been abstinent for at least 24 month. Exclusion Criteria: 1. Patients that do not consent to be involved in the trial, or whose parents do not consent for their children to be involved. 2. Patients or guardians of underage patients, with learning disabilities or other cognitive or sensory impairments that would prevent adequate understanding of the study requirements. 3. Patients who have had recent treatment (\<3 months), or are currently receiving treatment with antioxidants or magnesium tablets. 4. Patients who have had recent (\<3 months), or are currently receiving treatment with oral steroids for their pancreatic disease. 5. Patients with renal failure (serum creatinine 200 µg/l). 6. Patients with atrio-ventricular-block. 7. Serum triglyceride levels \>= 1000 mg/dl. 8. Patients under the age of five years or over the age of 75 years. 9. Patients who are dependent on daily opiate analgesia (morphine or equivalent) for more than 12 months. 10. Patients who have chronic hepatic failure, or serious impairment of pulmonary, cardiac, neurological or cerebral function. 11. Patients who are participating in another drug trial. 12. Patients who are pregnant. 13. Women of childbearing age who are not using contraception. 14. Lactating mothers. 15. Any disorder that would prevent adequate absorption of the active treatment.
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT00142233