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ACTIVE NOT RECRUITING
NCT04133792
PHASE3

Effect of Simvastatin on the Prognosis of Primary Primary Sclerosing Cholangitis (PSC)

Sponsor: Annika Bergquist

View on ClinicalTrials.gov

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

Interventions

DRUG

Simvastatin 40mg

40 mg orally daily for 5 years.

DRUG

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