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Telangiectasia, Hereditary HemorrhagicDAN-HEMTEL-VMNCT05933330

Hereditary Hemorrhagic Telangiectasia and Neurovascular Manifestations, in the Danish HHT Database

An observational study of Telangiectasia, Hereditary Hemorrhagic and Intracranial Arteriovenous Malformations, run by Odense University Hospital at 1 site in Denmark.

Active, not recruiting

Under way, not looking for participants. Everyone needed has enrolled. The study is still running.

Official record
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Trial summary

With a described prevalence of brain arteriovenous malformations (CAVM) of 12.8% in HHT patients, of whom 10% presents with intracranial hemorrhage, HHT pose a risk of devastating intracranial hemorrhage. Read more about this study

Who is it for?
Ages 18 to 65 years
What is being tested?
Brain MRI
How many people
300 participants
Where
1 siteDenmark
Study dates
1 Apr 2022to 31 Jul 2025
How long will I take part?
3 Years
Phase
Observational
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 to 65 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Patient with HHT (according to the curacao criteria or genetically verified mutations)

Who may be able to join

  • HHT according to the clinical diagnostic criteria (curacao)
  • 18-65 years of age.
  • registered in the Danish HHT-database

Who cannot join

  • patients has received an MRI of the brain with angio sequences, within the last 5 years.
  • contraindications to MRI
  • contraindications to self-reported questionnaires (i.e. mental retardation)

Trial locations and contacts

1 site in 1 country.

Denmark1 site
  • Danish HHT-center. Odense University Hospital

    Odense, Fyn, 5000

Other trials in Denmark

About this study

Official title: Hereditary Hemorrhagic Telangiectasia (HHT) and Its Diverse Neurological Manifestations: Unraveling the Intricacies of an Enigmatic Disorder

With a described prevalence of brain arteriovenous malformations (CAVM) of 12.8% in HHT patients, of whom 10% presents with intracranial hemorrhage, HHT pose a risk of devastating intracranial hemorrhage.

The main objective of the study is to challenge current statements (pros and cons) regarding systematic screening of asymptomatic HHT patients for neurovascular manifestations.

Read more

The investigators are thus seeking to answer a question many screening programs have faced.

A screening program should screen for a manageable problem, by a method that is considered cost effective and does not cause negative effect, even when extrapolated to a large cohort. Finally, the positive effect of screening program should outweigh the negative and not cause unnecessary concerns for the patients. The investigators are seeking to draw perspectives from the results to general questions about screening programs.

Read the detailed description

The Investigators are conducting a study investigating the disease, Hereditary Hemorrhagic Telangiectasia (HHT) and its neuro-logical and -vascular manifestations.

With a described prevalence of brain arteriovenous malformations (CAVM) of 12.8% in HHT patients, of whom 10% presents with intracranial hemorrhage, HHT pose a risk of devastating intracranial hemorrhage.

The main objective of the study is to challenge current statements (pros and cons) regarding systematic screening of asymptomatic HHT patients for neurovascular manifestations.

The investigators seek to fulfill the objective by offering all Danish HHT patients between 18-65 years of age, an MRI of the brain. Participants are asked to answer two questionnaires (SF-36 and BDI II) before and after the MRI. 100 participants are offered an MRI ASL in order, to investigate if this MRI sequence is more suitable to seek out vascular malformations of the brain.

The study is being performed at the University Hospital of Odense; participants receive their MRI at the radiological center closest to their home address. All participants are included, informed, and briefly interviewed over the telephone. Participants will be recruited using the Danish HHT database.

The project consist of 4 main parts.

  1. Neurological manifestations of HHT.
  2. A screening of all patients in the Danish HHT database, between 18-65 years of age for CAVM.
  3. A study of the adverse psychological effect from screening HHT patients in Denmark.
  4. An investigation of the optimal screening method for CAVM. Part 1
  • Data included in part study 1 is collected retrospectively from the prospectively maintained Danish HHT database. Neurological outcomes of all patients in the database, is cross-referenced with the Danish Apoplexy Register (DAP-database), to ensure optimal quality of registered neurological outcomes. Part 2
  • Data included in part study 2 is MRI of brain and surgical outcome. The proposed screening method will be conventional MRI, T1, T2 and TOF, of the cerebrum of all HHT patients between 18-65 years of age (n=350). 100 patients will be investigated further with MRI arterial spin labeling (ASL) and included in part 4. Part 3 • Data included in part study 3 is SF-36 and BDI II questionaires baseline and 3 months after patients have received an MRI of the brain. Part 4 • Data included in part study 4 is MRI of the brain, with comparative ASL sequencing. Separated in MRI with conventional sequences compared to MRI with ASL. Data will be reported according to: Reporting standards for angiographic evaluation and endovascular treatment of cerebral arteriovenous malformations, Jayaraman et al. (2011). A cost-effectiveness analysis, investigating to prize of an MRI, the cost of additional follow-up of vascular malformations and incidentalomas will be summarized in this part study. The data comes from Danish patients with HHT, 18-65 years of age. Continues data is expected to have normal distribution, and will be tested by the shapiro-wilk test. In case of normal distribution, oneway anova will be used to test significant levels of difference between the 5 groups (HHT1, HHT2, JP-HHT, Unknown HHT status and not genetically verified). If data is not normally distributed Kruskal-Wallis test will be used to test significance. Multivariate analyses will be done by logistic regression and in case of non-binary ordered data, ordered logistic regression adjusting for age and gender will be used. Dichotomous categorical data will be analyzed of their degree of independence with chi2 test. As HHT is inherited autosomal dominantly, and The sample group is only selected by age (18-65 years of age), The investigators expect data to have normal distribution. In case of lack of normal distribution, this could be explained by the fact that HHT is a rare disease with varying penetrance. A power analyses for the project shows: For the BDI II and SF-36 outcomes with 289 patients a mean change from pre-screening to post-screening could be detected with 80% power if:
  • Pre-post-correlation = 0.5 (assumed to be the lowest realistic value): Change of 0,17 SD could be detected
  • Pre-post-correlation = 0.8 (assumed to be the highest realistic value): Change of 0,10 SD could be detected As a clinical relevant difference typically would be assumed to be at least 0,3 SD, any clinical relevant changes should be detectable with 289 patients. A preliminary investigation indicates a 95% inclusion rate (5% of patients does not want to participate, or has already recieved an MRI of brain prior to the study). The investigators expect patients to be less likely to answer the questionnaire send to them 3 months after they have received the results from their brain MRI. Every Friday after initial invitation to the follow-up questionnaire, a reminder will be sent to the patients. after 3 reminders, the patients will finally be called. Part 4 - optimal MRI ASL (arterial spin labeling). In order for this study to be successful, The study need at least 10 patients whom have received a brain MRI with ASL that found a Cerebral AVM. In case of lacking case patients, HHT patients who have received an ordinary MRI with angio-sequences, that showed a cerebral AVM will be invited to have an brain MRI with ASL. This examination is done to uncover whether the participants have more cerebral AVM, that is not visible on conventional MRI. previous studies has shown, that roughly, 50% of HHT patients with cerebral AVM has multiple AVMs. The Danish HHT center has been situated at Odense University Hospital since 1996 and all HHT patients seen at the center have been included in the national research ´database. In 2015 data were uploaded in a Red Cap database and since then all patients included in the database have received written information and given informed consent. Data regarding date of birth, age, age of diagnosis, HHT type, results of screening for PAVM, CAVM and hepatic AVM (HAVM) are included. Furthermore, data regarding age of debut of epistaxis, results regarding date of neurological events, cerebral ischemia, bleeding, and abscess are also included in the Danish HHT database. The study and its part studies, contains personal patient data, and is therefore under the GDPR act. The project is approved by the Danish Data Protection Agency and the Region of Southern Denmark´s regional secretariat of Law. Data from this project is owned by the Danish HHT-center, and is located at the department of ear, nose and throat surgery at OUH. ALL data is only published in anonymized form. Data is only exported from RedCap in pseudononymized form for the purpose of statistical analyses.
Being tested
Brain MRI
Medical subject headings
Telangiectasia, Hereditary Hemorrhagic, Intracranial Arteriovenous Malformations

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Brain MRIOther

    All included patients receive an MRI of the brain

Study groups in NCT05933330
Study groupRoleWhat they receive
Danish HHT patient 18-65 years of ageNot described
Receives: Other: Brain MRI

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Number of new patients with Cerebral Arteriovenous malformation

    MRI verified arteriovenous malformation

    Measured: 1st of April 2022 - 30th of June 2025.

Secondary outcomes (5)
  1. Number of new patients with Ischemic stroke

    Symptomatic or silent (MRI verified) Ischemic cerebral stroke

    Measured: 1st of April 2022 - 30th of June 2025.

  2. Number of new patients with Hemorrhagic stroke

    spontaneous CAVM rupture.

    Measured: 1st of April 2022 - 30th of June 2025.

  3. Short Form 26

    Results from questionnaire SF-36. 0-100. 100 being the best possible.

    Measured: Baseline - inclusion, and 3 months after screening with MRI, and (in case of treatment) 3 months after treatment. 1st of April 2022 - 30th of June 2025.

  4. MRI arterial spin labeling (ASL)

    comparison between conventional MRI angio sequences compared to MRI with ASL, in it´s ability to detect CAVM.

    Measured: 1st of April 2022 - 30th of June 2025.

  5. Becks Depression Inventory II

    Results from questionnaire BDI II. 0-61. 61 being the most depressed possible, and 0 the "best".

    Measured: Baseline - inclusion, and 3 months after screening with MRI, and (in case of treatment) 3 months after treatment. 1st of April 2022 - 30th of June 2025.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 Jul 2023
  2. Study start1 Apr 2022
  3. Primary completion31 Mar 2025 (estimated)
  4. Study completion31 Jul 2025 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
300 participants (estimated)
Target duration
3 Years
IDs, dates and publications
ClinicalTrials.gov ID
NCT05933330
Sponsor's protocol ID
OP_1656
Acronym
DAN-HEMTEL-VM
Status last verified
Mar 2025
First submitted
15 Jun 2023
Last updated
30 Mar 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided: All data from the study, will be stored according to danish legislation and GDPR, in certified GDPR servers at OUH, after study completion.

Questions about this trial

What is this clinical trial studying?

An observational study of Telangiectasia, Hereditary Hemorrhagic and Intracranial Arteriovenous Malformations, run by Odense University Hospital at 1 site 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 3 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: under way, not looking for participants, as of the sponsor's last update on 30 Mar 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site 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?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Number of new patients with Cerebral Arteriovenous malformation (time frame: 1st of April 2022 - 30th of June 2025.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 30 Mar 2025.

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