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Effect of Simvastatin on the Prognosis of Primary Primary Sclerosing Cholangitis (PSC)
Sponsor: Annika Bergquist
Summary
This is a randomized, double-blind, placebo controlled multicenter study. A total of 700 patients will be included. After an updated powercalculation 560 was condidered enough The study will include patients with primary sclerosing cholangitis (PSC) for daily intake of 40 mg simvastatin/placebo for 5 years. The aim is to study effect of prognosis of PSC by long term intake of simvastatin. Outcome measures are death, liver transplantation, cholangiocarcinoma or bleeding from esophageal varices. Subjects will be randomized (1:1) between Simvastatin and placebo.
Official title: Effect of Simvastatin on the Prognosis of Primary Sclerosing Cholangitis (PSC); A Randomized, Double-blind, Placebo Controlled Multicenter Study
Key Details
Gender
All
Age Range
18 Years - 75 Years
Study Type
INTERVENTIONAL
Enrollment
571
Start Date
2020-10-01
Completion Date
2030-03-31
Last Updated
2025-09-05
Healthy Volunteers
No
Conditions
Interventions
Simvastatin 40mg
40 mg orally daily for 5 years.
Placebo oral tablet
40 mg orally daily for 5 years.
Locations (12)
Skåne Universitetssjukhus
Malmo, Skåne County, Sweden
Norrlands Universitetssjukhus
Umeå, Västerbotten County, Sweden
Sahlgrenska Universitetssjukhuset
Gothenburg, Västra Götaland County, Sweden
Sahlgrenska Universitetssjukhuset Östra
Gothenburg, Sweden
Karlstads centralsjukhus
Karlstad, Sweden
Skaraborgs sjukhus
Lidköping, Sweden
Örebro Universitetssjukhus
Örebro, Sweden
Karolinska University Hospital
Stockholm, Sweden
Karolinska University Hospital Solna
Stockholm, Sweden
Danderyds sjukhus
Stockholm, Sweden
Akademiska sjukhuset
Uppsala, Sweden
Universitetssjukhuset i Linköping
Linköping, Östergötland County, Sweden