Familial HypercholesterolemiaFINDNCT05614219
Familial Hypercholesterolemia Interpretive Comment - Nudging to Detection.
A study testing Biochemistry interpretive comment on elevated LDL-C levels in people with Familial Hypercholesterolemia, run by Odense University Hospital at 2 sites in Denmark.
Trial summary
Familial hypercholesterolemia is the most common inherited disease of the lipid metabolism, however it remains underdiagnosed. Only 15 % of 30.000 possible patients have been found in Denmark. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Familial Hypercholesterolemia
- What is being tested?
- Biochemistry interpretive comment on elevated LDL-C levels
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 2,000 participants
- Where
- 2 sitesDenmark
- Study dates
- 1 Dec 2023to 1 May 2027
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- All referred patients to the lipid clinics of Southern Denmark
- LDL-C ≥ 4 mmol/L in persons under the age of 40.
- LDL-C ≥ 5 mmol/L in persons ≥ 40 years.
Who cannot join
- Pregnancy and Secondary dyslipidemia
- Dysregulated diabetes. Hba1C < 48
- Dysregulated hypothyreosis. Elevated TSH.
- Kombined hyperlipidiemia TG > 4 mmol/L
- Nefrotic syndrome: proteinuria > 3 g/L and s-albumin < 30 g/l
- Cholestasis (alcalic fosfatase > 105 U/L and GGT > 55 U/L) 14 days prior to LDL-C measuring
- Pharmacological induced hyperlipidimia
Trial locations and contacts
2 sites in 1 country. Contact the study team or a site near you to ask about taking part.
Denmark2 sites, 2 recruiting
- Recruiting
Odense University Hospital
Odense, Funen, 5000
Jakob Knold, M.d., +4541278928, jakob.knold@rsyd.dk
Knold
- Recruiting
Departement of Cardiology, Odense University Hospital
Odense C, 5000
Finn Lund Henriksen, MD
About this study
Official title: Can Biochemistry Interpretive Comments on Elevated Cholesterol Levels, Increase Referrals to Lipid Clinics and Detection Rate of Familial Hypercholesterolemia? A Step Wedge Cluster Randomized Controlled Trial.
Familial hypercholesterolemia is the most common inherited disease of the lipid metabolism, however it remains underdiagnosed. Only 15 % of 30.000 possible patients have been found in Denmark. This quality assessing project will through a step wedge cluster randomized controlled trial evaluate establishment of a biochemistry interpretive comment on elevated LDL-C levels. The study will test if the comment results in an increase in referred patients to the lipid clinics of Southern Denmark as the primary endpoint, and as the secondary endpoint in more patients diagnosed with familial hypercholesterolemia. The project will run in totally 52 weeks and will in steps initiate the comment from the different laboratories in the Region of Southern Denmark.
Read the detailed description
Introduction:
Familial hypercholesterolemia (FH) is the most common inherited disease of the lipid metabolism with a prevalence of approximately 1/200. It is estimated that only 15 % of the estimated 30.000 patients in Denmark has been diagnosed. With high risk of atherosclerotic coronary disease, it is estimated that there is a great potential regarding cardiovascular health and health economics by early initiation of lipid lowering treatment and cascade screening of families.
All doctors can refer to lipid clinics on the suspicion of FH. FH should be suspected when low-density lipoprotein - cholesterol (LDL-C) is extremely elevated without any other explanation in young individuals, or in families with premature cardiovascular disease. The diagnosis is made from clinical scoring systems as the Simon Broome criteria, Dutch Lipid Clinical Network criteria and the MEDPED criteria including genetic test. The treatment is lipid-lowering drugs including statins, ezetimibe and PCSK9-inhibitor in case of insufficient effect.
In the last 12-14 years systematic cascade screening of FH families have been used in Denmark to track and find FH patients. The patients have since 2020 been registered in the National clinical quality database for FH.
However FH remains an under diagnosed disease, resulting in premature ischemic cardiovascular disease and premature cardiovascular death. Thus, there is a need for optimized screening for FH and more projects are already initiated.
Detecting more FH patients will demand an increased attention on elevated cholesterol. A biochemistry interpretive comment on elevated LDL-C according to the Danish FH Guideline regarding when to suspect FH, encouraging to further investigation for secondary dyslipidemia and successive referral to lipid clinic suspecting FH, can theoretically increase the awareness of FH. In England a survey has shown that general practitioners ask for interpretive comments on biochemistry analyses and 19 % of the general practitioners demands a comment on the lipid analyses.
A minor case control study in Australia have shown that interpretive comment on lipid profiles led to a significant reduction in LDL-C compared to controls, and increased the rate of referral by 11.5 % in cases compared to 1 % in controls, however only a minority was referred. The study was relatively small with 96 cases and 100 controls and an interpretive comment was activated when LDL-C > 6.5 mmol/L. However, the study is supported by a prospective case control study by the same research group including 231 patients with LDL-C > 6.5 mmol/L, where all doctors received an interpretive comment on elevated the LDL-C, raising suspicion to FH, but only cases received a comment which encouraged to referral to lipid clinic. Hereby 18 % of cases was referred compared to 8 % of controls. This indicates that in a minor population in another country, establishment of an interpretive comment on LDL-C could increase referral rate by 10 %. The prospective case control study concludes that the interpretive comment increases the detection rate of FH patients.
We want to evaluate implementation of an interpretive comment on elevated LDL-C levels in the Region of Southern Denmark. Compared to the Australian studies we expect to get more referrals since our cut-off for referral is lower (LDL-C 4 or 5 mmol/L depending on age). A strength in our study is the prospective step wedge RCT design.
Purpose and scientifically question:
This study will try to optimize screening for FH by investigating the effect of a biochemistry interpretive comment when LDL-C is significantly elevated according to the Danish FH guideline. The comment will encourage to further investigation and referral to local lipid clinic. The purpose is to test the effect of the interpretive comment regarding the proportion of patients referred to the lipid clinics as the primary endpoint. As the secondary endpoints we wish to calculate the change in LDL-C from referral to first contact in the lipid clinic, and the proportion of new diagnosed patients with FH at the lipid clinics in the Region of Southern Denmark.
This study will evaluate if it is possible to receive more referrals to the lipid clinics and find more patients with FH by an interpretive comment on cholesterol levels, encouraging to investigate for secondary dyslipidemia, and successive refer to lipid clinic in case of no explanation of the elevated LDL-C. The study will elucidate how many patients we have to refer, to find one patient with FH?
Method and material:
This study will through a step wedge cluster randomized controlled trial, investigate if establishment of the interpretive comment will result in more referrals and as the primary endpoint in more diagnosed patients with FH in the Region of Southern Denmark.
The material will consist of referred patients to the lipid clinics of Southern Denmark. The general practitioners and medical wards in the Region of Southern Denmark will be allocated in clusters according to the providing lab, totally 4 clusters. The clusters will be randomised to stepwise implementation of the biochemistry interpretive comment on cholesterol samples meeting the following criteria. FH should be suspected if LDL-C ≥ 4 mmol/L in persons under the age of 40, or LDL-C ≥ 5 mmol/L in persons ≥ 40 years of age according to the Danish guideline on FH. Randomization will be dobbeltblinded to data analyzing researchers and the general practitioners and wards receiving the interpretive comment.
The clusters will act as their own controls, the intervention being the biochemistry interpretive comment. The first cluster will implement the comment from the 01.12.2022 and after 12 weeks the next cluster will implement the comment. After 48 weeks all clusters will have implemented the interpretive comment. Further 8 weeks will act as buffer resulting in a totally study period of 52 weeks.
The Study will elucidate the proportion of referred patients and patients diagnosed with FH in the Region of Southern Denmark, after implementation of the interpretive comment.
The study will elucidate whether the proportion of referrals and diagnosed patients increases after implementation of the interpretive comment in the specific cluster or between the clusters.
The proportion of referred patients will be registered through data from the electronic patient journal system (EPJ). The reffered patients will be stratified both geographically and according to the referring physicians electronic laboratory system to account for bias regarding how the interpretive comment appears in the different systems, and whether this influence referral rate. The proportion of patients diagnosed with FH will be registered through ICD-10 codes in EPJ and crosschecked with Dutch Lipid Clinical score from the patient journal, including lipid profile and genetics to ensure a valid diagnosis. Furthermore HbA1c, TSH, liver- and kidney parameters and lipid profile will be registered as patient baseline characteristic to exclude patients with secondary dyslipidemia and to follow changes in LDL-C from referral to first lipid clinic contact. The study will furthermore elucidate how many patients there need to be referred to find one patient with FH.
Ethics
There is no need for information on an individual level, because the study is focusing on an organizational level as a step wedge cluster design. The patients can always deny further investigation or referral, and in this study we do not encourage to take blood samples without clinical indication. Instead we encourage through the biochemistry interpretive comment to act on blood samples already taken. The scientifically committee of Southern Denmark finds no indication for registration of the study because it is a study of assessing quality (Record number. S-20222000-106). The study will be registered in the Region of Southern Denmarks list of Research projects.
- Conditions
- Familial Hypercholesterolemia
- Being tested
- Biochemistry interpretive comment on elevated LDL-C levels
- Keywords
- Familial Hypercholesterolemia, Biochemistry interpretive comment, Low-density lipoprotein cholesterol levels, Screening
- Medical subject headings
- Hyperlipoproteinemia Type II
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Biochemistry interpretive comment on elevated LDL-C levelsOther
The interpretive comment on LDL-C will encourage for excluding secondary dyslipidemia (measuring Hba1C, TSH and checking current drugs and talk about diet). If secondary dyslipidemia ca be excluded we encourage to referral to lipid clinic. Familial hypercholesterolemia should be suspected if LDL-C ≥ 4 mmol/L in persons under the age of 40, or LDL-C ≥ 5 mmol/L in persons ≥ 40. The biochemistry interpretive comment will thus be released to the referring physician if the blood sample meet the criteria above. We advice that in pregnant women to control elevated LDL-C after childbirth.
| Study group | Role | What they receive |
|---|---|---|
| Biochemistry interpretive comment on LDL-C levels | Experimental | The general practitioners and hospital wards will be allocated in cluster according to their providing lab, and stepwise implement the comment on LDL-C ≥ 4 mmol/L in persons under the age of 40 and ≥ 5 mmol/L in persons ≥ 40 years. Raising awareness on familial hypercholesterolemia an encouraging to referral.
Cluster 1. Will from the 01.12.2022 implement comment on LDL-C Cluster 2. Will from the 01.03.2023 implement comment on LDL-C Cluster 3. Will from the 01.06.2023 implement comment on LDL-C Cluster 4.Will from the 01.09.2023 implement comment on LDL-C Receives: Other: Biochemistry interpretive comment on elevated LDL-C levels |
| Control | No intervention | The clusters will act as their own controls, due to the stepwise implementation of the comment. Cluster 2: Will not implement the comment before the 01.03.2023 Cluster 3: Will not implement the comment before the 01.06.2023 Cluster 4: Will not implement the comment before the 01.09.2023 |
What is being measured
The primary outcome is the main question the study is designed to answer.
Number of patients reffered to lipid clinic
Proportion of referred patients to lipid clinics in the region of Southern Denmark after establishment of interpretive comment on LDL-C, compared to proportion before the comment.
Measured: 12-18 months
Diagnosed patients with Familial Hyperchoelsterolemia
Proportion of patients diagnosed with familial hypercholesterolemia (Dutch clinical lipid score ≥ 6) in the Region of Southern Denmark after establishment of interpretive comment on LDL-C, compared to proportion before the comment.
Measured: During 9-12 months due to waiting time for genetic test
Secondary outcomes (7)
Change in LDL-C
Change in LDL-C levels from referral to first contact in lipid clinic
Measured: 3-6 months
Familial hypercholesterolemia mutations
Number of genetic test with mutations related to familial hypercholesterolemia
Measured: 9-12 months due to waiting time for genetic test
Hba1C
Mean Hba1C at referral as baseline value
Measured: 3 months
TSH
Mean TSH at referral as baseline value
Measured: 3 months
Triglycerides
Mean triglycerides at referral as baseline value and change in triglycerides at first visit in lipid clinic.
Measured: 3 months
HDL-Cholesterol
Mean HDL-Cholesterol at referral as baseline value and change in HDL-Cholesterol at first visit in lipid clinic.
Measured: 3 months
Lipoprotein(a)
Mean Lipoprotein(a) as a baseline value
Measured: 3 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted14 Nov 2022
- Study start1 Dec 2023
- Primary completion1 May 2027 (estimated)
- Study completion1 May 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (10)Papers the sponsor has linked to this study.
- Other trials for Familial HypercholesterolemiaStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Screening
- Allocation
- Randomised
- Intervention model
- Sequential
- Model description
- Step wedge cluster randomized controlled trial.
- Masking
- None (open label)
- Enrolment
- 2,000 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Odense University Hospital
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Jakob Knold, Odense University Hospital
- Investigators
- Finn Lund Henriksen, Ph.d., Principal investigator, Departement of Cardiology, Odense University Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05614219
- Sponsor's protocol ID
- FINDRSYD22
- Acronym
- FIND
- Status last verified
- Feb 2026
- First submitted
- 27 Oct 2022
- Last updated
- 20 Feb 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: The results will be published and shared in an international peer reviewed journal.
Publications
Levenson AE, de Ferranti SD. Familial Hypercholesterolemia. In: Feingold KR, Anawalt B, Boyce A, Chrousos G, de Herder WW, Dhatariya K, et al., editors. Endotext. South Dartmouth (MA)2000.
Bundgaard H SMea. Regionernes klinisk kvalitetsdatabase. Familiær hyperkolesterolæmi databasen. 2020 [Available from: https://www.rkkp.dk/kvalitetsdatabaser/databaser/databasen-for-familiaer-hyperkolesterolaemi/
Rosso A, Pitini E, D'Andrea E, Massimi A, De Vito C, Marzuillo C, Villari P. The Cost-effectiveness of Genetic Screening for Familial Hypercholesterolemia: a Systematic Review. Ann Ig. 2017 Sep-Oct;29(5):464-480. doi: 10.7416/ai.2017.2178.
PubMed 28715059Sturm AC, Knowles JW, Gidding SS, Ahmad ZS, Ahmed CD, Ballantyne CM, Baum SJ, Bourbon M, Carrie A, Cuchel M, de Ferranti SD, Defesche JC, Freiberger T, Hershberger RE, Hovingh GK, Karayan L, Kastelein JJP, Kindt I, Lane SR, Leigh SE, Linton MF, Mata P, Neal WA, Nordestgaard BG, Santos RD, Harada-Shiba M, Sijbrands EJ, Stitziel NO, Yamashita S, Wilemon KA, Ledbetter DH, Rader DJ; Convened by the Familial Hypercholesterolemia Foundation. Clinical Genetic Testing for Familial Hypercholesterolemia: JACC Scientific Expert Panel. J Am Coll Cardiol. 2018 Aug 7;72(6):662-680. doi: 10.1016/j.jacc.2018.05.044.
PubMed 30071997Raal FJ, Hovingh GK, Catapano AL. Familial hypercholesterolemia treatments: Guidelines and new therapies. Atherosclerosis. 2018 Oct;277:483-492. doi: 10.1016/j.atherosclerosis.2018.06.859.
PubMed 30270089Hedegaard BS. A danish nationwide study og individuals suspected of FH referred from general practice to lipid clinics: Clinical characteristics, plasma lpipoprotein(A) and final diagnosis. Atherosclerosis. 2021.
Schmidt EB, Hedegaard BS, Retterstol K. Familial hypercholesterolaemia: history, diagnosis, screening, management and challenges. Heart. 2020 Dec;106(24):1940-1946. doi: 10.1136/heartjnl-2019-316276. Epub 2020 Sep 15. No abstract available.
PubMed 32933999Schmidt EB, Henriksen FL, Kanstrup HL. Familiær hyperkolesterolæmi holdningspapir Dansk Cardiologisk Selskab2019 [08.04. 2022]. Available from: https://nbv.cardio.dk/media/com_reditem/files/customfield/item/7349/601670e648780b94c9cf26375caef524dcdb2270.pdf
Barlow IM. Are biochemistry interpretative comments helpful? Results of a general practitioner and nurse practitioner survey. Ann Clin Biochem. 2008 Jan;45(Pt 1):88-90. doi: 10.1258/acb.2007.007134.
PubMed 18275680Hemming K, Haines TP, Chilton PJ, Girling AJ, Lilford RJ. The stepped wedge cluster randomised trial: rationale, design, analysis, and reporting. BMJ. 2015 Feb 6;350:h391. doi: 10.1136/bmj.h391. No abstract available.
PubMed 25662947
Study at a glance
From the registry record, last updated by the sponsor on 20 Feb 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Can Biochemistry Interpretive Comments on Elevated Cholesterol Levels, Increase Referrals to Lipid Clinics and Detection Rate of Familial Hypercholesterolemia? A Step Wedge Cluster Randomized Controlled Trial.
- ClinicalTrials.gov ID
- NCT05614219
- Acronym / sponsor ID
- FIND / FINDRSYD22
- Conditions
- Familial Hypercholesterolemia
- Keywords
- Familial Hypercholesterolemia, Biochemistry interpretive comment, Low-density lipoprotein cholesterol levels, Screening
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 2,000 participants (estimated)
- Lead sponsor
- Odense University HospitalUniversity, hospital or other
- Study start
- 1 Dec 2023 (actual)
- Primary completion
- 1 May 2027 (estimated)
- Study completion
- 1 May 2027 (estimated)
- First posted
- 14 Nov 2022 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Familial hypercholesterolemia is the most common inherited disease of the lipid metabolism, however it remains underdiagnosed. Only 15 % of 30.000 possible patients have been found in Denmark. This quality assessing project will through a step wedge cluster randomized controlled trial evaluate establishment of a biochemistry interpretive comment on elevated LDL-C levels. The study will test if the comment results in an increase in referred patients to the lipid clinics of Southern Denmark as the primary endpoint, and as the secondary endpoint in more patients diagnosed with familial hypercholesterolemia. The project will run in totally 52 weeks and will in steps initiate the comment from the different laboratories in the Region of Southern Denmark.
Detailed description
Introduction:
Familial hypercholesterolemia (FH) is the most common inherited disease of the lipid metabolism with a prevalence of approximately 1/200. It is estimated that only 15 % of the estimated 30.000 patients in Denmark has been diagnosed. With high risk of atherosclerotic coronary disease, it is estimated that there is a great potential regarding cardiovascular health and health economics by early initiation of lipid lowering treatment and cascade screening of families.
All doctors can refer to lipid clinics on the suspicion of FH. FH should be suspected when low-density lipoprotein - cholesterol (LDL-C) is extremely elevated without any other explanation in young individuals, or in families with premature cardiovascular disease. The diagnosis is made from clinical scoring systems as the Simon Broome criteria, Dutch Lipid Clinical Network criteria and the MEDPED criteria including genetic test. The treatment is lipid-lowering drugs including statins, ezetimibe and PCSK9-inhibitor in case of insufficient effect.
In the last 12-14 years systematic cascade screening of FH families have been used in Denmark to track and find FH patients. The patients have since 2020 been registered in the National clinical quality database for FH.
However FH remains an under diagnosed disease, resulting in premature ischemic cardiovascular disease and premature cardiovascular death. Thus, there is a need for optimized screening for FH and more projects are already initiated.
Detecting more FH patients will demand an increased attention on elevated cholesterol. A biochemistry interpretive comment on elevated LDL-C according to the Danish FH Guideline regarding when to suspect FH, encouraging to further investigation for secondary dyslipidemia and successive referral to lipid clinic suspecting FH, can theoretically increase the awareness of FH. In England a survey has shown that general practitioners ask for interpretive comments on biochemistry analyses and 19 % of the general practitioners demands a comment on the lipid analyses.
A minor case control study in Australia have shown that interpretive comment on lipid profiles led to a significant reduction in LDL-C compared to controls, and increased the rate of referral by 11.5 % in cases compared to 1 % in controls, however only a minority was referred. The study was relatively small with 96 cases and 100 controls and an interpretive comment was activated when LDL-C > 6.5 mmol/L. However, the study is supported by a prospective case control study by the same research group including 231 patients with LDL-C > 6.5 mmol/L, where all doctors received an interpretive comment on elevated the LDL-C, raising suspicion to FH, but only cases received a comment which encouraged to referral to lipid clinic. Hereby 18 % of cases was referred compared to 8 % of controls. This indicates that in a minor population in another country, establishment of an interpretive comment on LDL-C could increase referral rate by 10 %. The prospective case control study concludes that the interpretive comment increases the detection rate of FH patients.
We want to evaluate implementation of an interpretive comment on elevated LDL-C levels in the Region of Southern Denmark. Compared to the Australian studies we expect to get more referrals since our cut-off for referral is lower (LDL-C 4 or 5 mmol/L depending on age). A strength in our study is the prospective step wedge RCT design.
Purpose and scientifically question:
This study will try to optimize screening for FH by investigating the effect of a biochemistry interpretive comment when LDL-C is significantly elevated according to the Danish FH guideline. The comment will encourage to further investigation and referral to local lipid clinic. The purpose is to test the effect of the interpretive comment regarding the proportion of patients referred to the lipid clinics as the primary endpoint. As the secondary endpoints we wish to calculate the change in LDL-C from referral to first contact in the lipid clinic, and the proportion of new diagnosed patients with FH at the lipid clinics in the Region of Southern Denmark.
This study will evaluate if it is possible to receive more referrals to the lipid clinics and find more patients with FH by an interpretive comment on cholesterol levels, encouraging to investigate for secondary dyslipidemia, and successive refer to lipid clinic in case of no explanation of the elevated LDL-C. The study will elucidate how many patients we have to refer, to find one patient with FH?
Method and material:
This study will through a step wedge cluster randomized controlled trial, investigate if establishment of the interpretive comment will result in more referrals and as the primary endpoint in more diagnosed patients with FH in the Region of Southern Denmark.
The material will consist of referred patients to the lipid clinics of Southern Denmark. The general practitioners and medical wards in the Region of Southern Denmark will be allocated in clusters according to the providing lab, totally 4 clusters. The clusters will be randomised to stepwise implementation of the biochemistry interpretive comment on cholesterol samples meeting the following criteria. FH should be suspected if LDL-C ≥ 4 mmol/L in persons under the age of 40, or LDL-C ≥ 5 mmol/L in persons ≥ 40 years of age according to the Danish guideline on FH. Randomization will be dobbeltblinded to data analyzing researchers and the general practitioners and wards receiving the interpretive comment.
The clusters will act as their own controls, the intervention being the biochemistry interpretive comment. The first cluster will implement the comment from the 01.12.2022 and after 12 weeks the next cluster will implement the comment. After 48 weeks all clusters will have implemented the interpretive comment. Further 8 weeks will act as buffer resulting in a totally study period of 52 weeks.
The Study will elucidate the proportion of referred patients and patients diagnosed with FH in the Region of Southern Denmark, after implementation of the interpretive comment.
The study will elucidate whether the proportion of referrals and diagnosed patients increases after implementation of the interpretive comment in the specific cluster or between the clusters.
The proportion of referred patients will be registered through data from the electronic patient journal system (EPJ). The reffered patients will be stratified both geographically and according to the referring physicians electronic laboratory system to account for bias regarding how the interpretive comment appears in the different systems, and whether this influence referral rate. The proportion of patients diagnosed with FH will be registered through ICD-10 codes in EPJ and crosschecked with Dutch Lipid Clinical score from the patient journal, including lipid profile and genetics to ensure a valid diagnosis. Furthermore HbA1c, TSH, liver- and kidney parameters and lipid profile will be registered as patient baseline characteristic to exclude patients with secondary dyslipidemia and to follow changes in LDL-C from referral to first lipid clinic contact. The study will furthermore elucidate how many patients there need to be referred to find one patient with FH.
Ethics
There is no need for information on an individual level, because the study is focusing on an organizational level as a step wedge cluster design. The patients can always deny further investigation or referral, and in this study we do not encourage to take blood samples without clinical indication. Instead we encourage through the biochemistry interpretive comment to act on blood samples already taken. The scientifically committee of Southern Denmark finds no indication for registration of the study because it is a study of assessing quality (Record number. S-20222000-106). The study will be registered in the Region of Southern Denmarks list of Research projects.
Study design
- Primary purpose
- Screening
- Allocation
- Randomised
- Intervention model
- Sequential
- Masking
- None (open label)
- Number of arms
- 2
- Model description
- Step wedge cluster randomized controlled trial.
| Arm | Type | Receives |
|---|---|---|
| Biochemistry interpretive comment on LDL-C levels | Experimental | Other: Biochemistry interpretive comment on elevated LDL-C levelsThe general practitioners and hospital wards will be allocated in cluster according to their providing lab, and stepwise implement the comment on LDL-C ≥ 4 mmol/L in persons under the age of 40 and ≥ 5 mmol/L in persons ≥ 40 years. Raising awareness on familial hypercholesterolemia an encouraging to referral. Cluster 1. Will from the 01.12.2022 implement comment on LDL-C Cluster 2. Will from the 01.03.2023 implement comment on LDL-C Cluster 3. Will from the 01.06.2023 implement comment on LDL-C Cluster 4.Will from the 01.09.2023 implement comment on LDL-C |
| Control | No intervention | –The clusters will act as their own controls, due to the stepwise implementation of the comment. Cluster 2: Will not implement the comment before the 01.03.2023 Cluster 3: Will not implement the comment before the 01.06.2023 Cluster 4: Will not implement the comment before the 01.09.2023 |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- All referred patients to the lipid clinics of Southern Denmark
- LDL-C ≥ 4 mmol/L in persons under the age of 40.
- LDL-C ≥ 5 mmol/L in persons ≥ 40 years.
Key exclusion criteria (7 listed)
- Pregnancy and Secondary dyslipidemia
- Dysregulated diabetes. Hba1C < 48
- Dysregulated hypothyreosis. Elevated TSH.
- Kombined hyperlipidiemia TG > 4 mmol/L
- Nefrotic syndrome: proteinuria > 3 g/L and s-albumin < 30 g/l
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Biochemistry interpretive comment on elevated LDL-C levelsThe interpretive comment on LDL-C will encourage for excluding secondary dyslipidemia (measuring Hba1C, TSH and checking current drugs and talk about diet). If secondary dyslipidemia ca be excluded we encourage to referral to lipid clinic. Familial hypercholesterolemia should be suspected if LDL-C ≥ 4 mmol/L in persons under the age of 40, or LDL-C ≥ 5 mmol/L in persons ≥ 40. The biochemistry interpretive comment will thus be released to the referring physician if the blood sample meet the criteria above. We advice that in pregnant women to control elevated LDL-C after childbirth. | Other | Biochemistry interpretive comment on LDL-C levels |
Primary outcome
Number of patients reffered to lipid clinic
Time frame: 12-18 months
Proportion of referred patients to lipid clinics in the region of Southern Denmark after establishment of interpretive comment on LDL-C, compared to proportion before the comment.
Diagnosed patients with Familial Hyperchoelsterolemia
Time frame: During 9-12 months due to waiting time for genetic test
Proportion of patients diagnosed with familial hypercholesterolemia (Dutch clinical lipid score ≥ 6) in the Region of Southern Denmark after establishment of interpretive comment on LDL-C, compared to proportion before the comment.
7 secondary outcomes
Change in LDL-C
Time frame: 3-6 months
Familial hypercholesterolemia mutations
Time frame: 9-12 months due to waiting time for genetic test
Hba1C
Time frame: 3 months
TSH
Time frame: 3 months
Triglycerides
Time frame: 3 months
HDL-Cholesterol
Time frame: 3 months
Lipoprotein(a)
Time frame: 3 months
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 20 Feb 2026.
- BackgroundLevenson AE, de Ferranti SD. Familial Hypercholesterolemia. In: Feingold KR, Anawalt B, Boyce A, Chrousos G, de Herder WW, Dhatariya K, et al., editors. Endotext. South Dartmouth (MA)2000.
- BackgroundBundgaard H SMea. Regionernes klinisk kvalitetsdatabase. Familiær hyperkolesterolæmi databasen. 2020 [Available from: https://www.rkkp.dk/kvalitetsdatabaser/databaser/databasen-for-familiaer-hyperkolesterolaemi/
- Background: PubMed 28715059Rosso A, Pitini E, D'Andrea E, Massimi A, De Vito C, Marzuillo C, Villari P. The Cost-effectiveness of Genetic Screening for Familial Hypercholesterolemia: a Systematic Review. Ann Ig. 2017 Sep-Oct;29(5):464-480. doi: 10.7416/ai.2017.2178.
- Background: PubMed 30071997Sturm AC, Knowles JW, Gidding SS, Ahmad ZS, Ahmed CD, Ballantyne CM, Baum SJ, Bourbon M, Carrie A, Cuchel M, de Ferranti SD, Defesche JC, Freiberger T, Hershberger RE, Hovingh GK, Karayan L, Kastelein JJP, Kindt I, Lane SR, Leigh SE, Linton MF, Mata P, Neal WA, Nordestgaard BG, Santos RD, Harada-Shiba M, Sijbrands EJ, Stitziel NO, Yamashita S, Wilemon KA, Ledbetter DH, Rader DJ; Convened by the Familial Hypercholesterolemia Foundation. Clinical Genetic Testing for Familial Hypercholesterolemia: JACC Scientific Expert Panel. J Am Coll Cardiol. 2018 Aug 7;72(6):662-680. doi: 10.1016/j.jacc.2018.05.044.
- Background: PubMed 30270089Raal FJ, Hovingh GK, Catapano AL. Familial hypercholesterolemia treatments: Guidelines and new therapies. Atherosclerosis. 2018 Oct;277:483-492. doi: 10.1016/j.atherosclerosis.2018.06.859.
- BackgroundHedegaard BS. A danish nationwide study og individuals suspected of FH referred from general practice to lipid clinics: Clinical characteristics, plasma lpipoprotein(A) and final diagnosis. Atherosclerosis. 2021.
- Background: PubMed 32933999Schmidt EB, Hedegaard BS, Retterstol K. Familial hypercholesterolaemia: history, diagnosis, screening, management and challenges. Heart. 2020 Dec;106(24):1940-1946. doi: 10.1136/heartjnl-2019-316276. Epub 2020 Sep 15. No abstract available.
- BackgroundSchmidt EB, Henriksen FL, Kanstrup HL. Familiær hyperkolesterolæmi holdningspapir Dansk Cardiologisk Selskab2019 [08.04. 2022]. Available from: https://nbv.cardio.dk/media/com_reditem/files/customfield/item/7349/601670e648780b94c9cf26375caef524dcdb2270.pdf
- Background: PubMed 18275680Barlow IM. Are biochemistry interpretative comments helpful? Results of a general practitioner and nurse practitioner survey. Ann Clin Biochem. 2008 Jan;45(Pt 1):88-90. doi: 10.1258/acb.2007.007134.
- Background: PubMed 25662947Hemming K, Haines TP, Chilton PJ, Girling AJ, Lilford RJ. The stepped wedge cluster randomised trial: rationale, design, analysis, and reporting. BMJ. 2015 Feb 6;350:h391. doi: 10.1136/bmj.h391. No abstract available.
- Individual participant dataSharing planned: No. The results will be published and shared in an international peer reviewed journal.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Finn Lund Henriksen, Ph.d. principal investigator
Departement of Cardiology, Odense University Hospital
2 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Biochemistry interpretive comment on elevated LDL-C levels in people with Familial Hypercholesterolemia, run by Odense University Hospital at 2 sites in Denmark.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 20 Feb 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 2 sites in Denmark. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Jakob Knold, MD (004541278928, jakobknold@rsyd.dk), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Number of patients reffered to lipid clinic (time frame: 12-18 months). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT05614219, which also lists 10 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Feb 2026.