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2023-507489-20-00RecruitingPhase 4

Optimizing therapy with n=1-studies: negating the 'nocebo' effect in statin-intolerance

N=1-studies In Statin-intolerance; Objectifying Nocebo Effects (NISONE)

Source: EU CTIS (euclinicaltrials.eu) · Last updated 27 Aug 2026

Next steps

Brief summary (registry, in English)

The key objective of the study is to assess whether an ‘n=1 study’ (randomized, double blind, cross-over trial with counseling on patients’ individual treatment results) will increase statin use and reduce the prescription of PCSK9i compared to usual care at 12 months (t12m) after randomization.

Status (registry)
Recruiting
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
249 (estimated)
First submitted
10 Jun 2024
Start date
10 Dec 2024
Lead sponsor
Erasmus Universitair Medisch Centrum Rotterdam (Erasmus MC)
EU CT number
2023-507489-20-00

What you commit to

  • Study type: Interventional · Phase 4
  • Planned participants: 249
  • 11 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study design.

AI-kivonat: who the study is looking for

Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adults with heart disease or familial hypercholesterolemia who stopped statins because of side effects, to test whether an n=1 study helps them take statins again.

Age
18 years or older
Sex
All sexes can join.
Disease stage
Previous cardiovascular disease, or familial hypercholesterolemia (both primary and secondary prevention), with a need for cholesterol-lowering treatment.
Earlier treatment
Must have taken two or more statins and stopped them because of (perceived) side effects.

Main reasons for not taking part

  • Previous statin use that caused a severe allergic reaction, muscle damage, abnormal liver tests or other severe health problems
  • Pregnancy, planned pregnancy within 12 months, or breastfeeding
  • History of muscle disease, long-lasting severe pain, severe mental illness, cirrhosis or severe kidney problems
  • A cardiovascular event in the past 3 months
  • No digital access, or not enough Dutch or English to fill in the questionnaires

Read by machine on 9 Nov 2026.

Who cannot take part

Copied verbatim from EU CTIS (euclinicaltrials.eu) and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Clinical judgement of the health care professional that LDL-c lowering therapy cannot be withheld in a patient with a recent cardiovascular event in the past 12 months.

Other illness

  • History of myopathy or any other condition that causes severe chronic pain.
  • History of severe mental illness (as their experience of symptoms may already be altered).
  • Clinical judgement of the health care professional that LDLc-lowering therapy is not relevant for the prognosis (e.g. severe frailty, dementia, end-stage heart failure, end-stage malignancy).

Lab values

  • A contra-indication for rosuvastatin therapy related to: a. Previous statin use causing anaphylaxis or other moderate/severe allergic reaction. b. Previous statin use causing myopathy (serum rise of creatine kinase more than 3 times the upper limit of normal) or rhabdomyolysis. c. Previous statin use with liver function abnormalities, defined as aspartate aminotransferase (AST) or alanine aminotransferase >3 times the upper limit of normal. d. Previous statins use causing severe health issues. e. Planned pregnancy within 12 months, pregnancy or breastfeeding. f. Currently taking other drugs with known relevant interactions to rosuvastatin as listed in the Investigational Medicinal Product Dossier (IMPD). g. Any other contraindication for rosuvastatin as listed in the Investigational Medicinal Product Dossier (IMPD).
  • History of cirrhosis or severe renal insufficiency (eGFR < 20 ml/min/1,73m2)

Other

  • Insufficient ability to fill in questionnaires in the digital platform; a. No access to a smartphone, tablet or personal computer. b. Insufficient understanding of the Dutch or English language.
  • A recent cardiovascular event in the past 3 months.
  • Clinical judgement of the health care professional who considers participation unethical or otherwise unwanted.

Who the study is looking for

  • Aged 18 years or older.
  • Previously taken two or more statins and withdrawn from statins because of (perceived) side effects.
  • Clinical indication for lipid lowering therapy related to secondary prevention of cardiovascular disease (previous CVD) or prevention of cardiovascular disease (both primary and secondary) in familial hypercholesterolemia.
  • Provided full informed consent.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on EU CTIS (euclinicaltrials.eu)

Sites (11)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Meander Medisch CentrumAmersfoortNetherlandsRecruiting
Rijnstate Ziekenhuis StichtingArnhemNetherlandsRecruiting
Albert Schweitzer ZiekenhuisDordrechtNetherlandsRecruiting
Ziekenhuis Gelderse Vallei StichtingEde GldNetherlandsRecruiting
Radboud Universitair Medisch Centrum (Radboudumc)NijmegenNetherlandsRecruiting
Maasstad Ziekenhuis StichtingRotterdamNetherlandsRecruiting
Sint Franciscus Vlietland Groep StichtingRotterdamNetherlandsRecruiting
Erasmus Universitair Medisch Centrum Rotterdam (Erasmus MC)RotterdamNetherlandsRecruiting
Stichting Elisabeth-TweeSteden ZiekenhuisTilburgNetherlandsRecruiting
Universitair Medisch Centrum UtrechtUtrechtNetherlandsRecruiting
Isala Klinieken StichtingZwolleNetherlandsRecruiting

Are you the coordinator? Confirm the details

This page is information, not medical advice. Discuss any trial with your doctor.