Hereditary Angioedema Type I and IIHGRNCT03828279
Global Registry to Gather Data on Natural History of Patients With Hereditary Angioedema Type I and II
An observational study of Hereditary Angioedema Type I and II, run by HAE Global Registry Foundation at 1 site in Italy.
Trial summary
The objective of this international hereditary angioedema (HAE) register is to collect homogeneous clinical and laboratory data on patients with HAE type I and II gathering better information on the natural course of the disease and detecting therapeutic options to manage it. Read more about this study
- Who is it for?
- Any ageHealthy volunteers can take part
- Conditions the study is for
- Hereditary Angioedema Type I and II
- What is being tested?
- functional and antigenic C1 inhibitor
- How many people
- 220 participants
- Where
- 1 siteItaly
- Study dates
- 1 Oct 2017to 31 Dec 2023
- How long will I take part?
- 1 Year
- Phase
- Observational
- Are there results?
- None posted in the registry
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 Any age
- All sexes
- Healthy volunteers accepted
- Child, Adult, Older adult
Study population: patients diagnosed with HAE type I and II and followed by a referral center for angioedema
Who may be able to join
- patients diagnosed with HAE type I and II with signed informed consent
- laboratory diagnostic criteria documenting plasma levels of C1 inhibitor antigen and function and of C4 antigen
Who cannot join
- patients without HAE type I and II
- patients without documented laboratory diagnostic criteria
- patients not capable to give informed consent
Trial locations and contacts
1 site in 1 country.
Italy1 site, 1 recruiting
- Recruiting
ASST FBF Sacco
Milan, 20157
marco cicardi, M.D., +3950319829, marco.cicardi@unimi.it
About this study
Official title: The Global Registry on Hereditary Angioedema Type I and II
The objective of this international hereditary angioedema (HAE) register is to collect homogeneous clinical and laboratory data on patients with HAE type I and II gathering better information on the natural course of the disease and detecting therapeutic options to manage it.
Read the detailed description
It is an international multicenter disease registry, the principal investigator at each center is responsible for competent ethic committee/institutional review board approval and for identifying co-investigators, who collect patients' informed consent and insert patients' data. Participating patients own their data. Upon acceptance of the informed consent, the treating physician transfers data of the case report form (CRF) to a specifically designed electronic support (eCRF) and the patients enter data on attacks. Physicians at center fill-in the eCRF with data for demography, diagnosis, prophylaxis and associated diseases. Plasma levels of C1 inhibitor antigen and function and of C4 antigen document laboratory diagnostic criteria. Each patient has a national identifier code. Patients fill-in attack reports that encompass duration, severity and treatment of each angioedema episode. C1 inhibitor coding gene (SERPING1) genotype is entered according to the last Hugo nomenclature. Yearly update of information is recommended, patients with follow up above two years are moved in a separate area and excluded from analysis. Each patient prospectively fills data on attacks. On a specific informed consent, the patient can agree on storing biological material (plasma and nucleic acids) for research purposes.
The data processor is an innovative start-up (Cloud-R s.r.l. Milan, Italy) that manages all data according to a specific contract and in compliance with current regulation on sensitive data security and processing. The Registry, delivered in the mode of Registry-as-a-Service (RaaS), is designed following General Data Protection Regulation (GDPR) guidelines, and issues regular software and infrastructure enhancements as a part of the normal operational mode. The system generates statistics of aggregated anonymized data following the participating centers' hierarchy levels and Global Registry governance rules. Patients supply data on attacks either on paper support or using a Web form or a mobile application. These data will flow into a staging area for physician validation before being considered valid for statistics. For each entry the system updates in real-time all the statistics and dashboards. The platform has configurable functionalities to support data quality management. It provides data format validation, integration to external qualified libraries, alerts, dashboards, automatic index calculations, advanced filters and queries, data change log. This open architecture, allows integration of the system, via standard API's, to external or sub-registries, registries, biobanks and clinical bioinformatics tools, i.e. for specific trial studies leveraging a specific cluster of patients already present in the Global Registry.
An independent non-profit foundation (HGRF) made of representatives of patients' associations is in charge for funding and delegates all the management to the HAE Global Registry Board (HGRB). The HGRB is in charge for operational, assisted by the HAE Global Registry Scientific Committee (HGRSC) for topics of competence. No registry member, center, group or board can access the entire set of data. All registry members, as single or group, can propose studies based on aggregated data by addressing the request to the HGRSC. Analysis and studies of data at local centers can occur at any time. Members of HGRB and HGRSC are elected to be representative of different cultural and geographic backgrounds. Their offices have a two-year term with no more than one consecutive renewal. Angioedema centers can join the Registry upon request to the HGRB . The registry quality control system periodically checks Registry entries and compliance of eCRF with the source data. For each information, the system will grant traceability of time and author.
- Conditions
- Hereditary Angioedema Type I and II
- Being tested
- functional and antigenic C1 inhibitor
- Keywords
- angioedema, disease registry, C1 inhibitor, anti bradykinin treatments
- Medical subject headings
- Hereditary Angioedema Types I and II, Angioedema, Angioedemas, Hereditary
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
functional and antigenic C1 inhibitorDiagnostic test
Also called genetic analysis
Diagnosis of HAE is based on personal and/or family history of angioedema and on C1 inhibitor functional or antigenic plasma levels ≤50% of normal.
| Study group | Role | What they receive |
|---|---|---|
| hereditary angioedema type I | Patients were diagnosed as C1 inhibitor HAE type I when functional and antigenic C1 inhibitor were ≤ 50% of normal Receives: Diagnostic Test: functional and antigenic C1 inhibitor | |
| hereditary angioedema type II | Patients were diagnosed as type II when functional C1 inhibitor was ≤50% and antigenic was >50% of normal Receives: Diagnostic Test: functional and antigenic C1 inhibitor |
What is being measured
The primary outcome is the main question the study is designed to answer.
Number of angioedema events
Number of angioedema events
Measured: Through study completion, an average of 5 years
Time of angioedema events
Time in hours of presence of angioedema symptoms
Measured: Through study completion, an average of 5 years
Severity of angioedema events
Number of severe, moderate, mild angioedema symptoms based on a three point scale patient reported outcome
Measured: through study completion, an average of 5 years
Secondary outcomes (3)
Comorbidities
Number and type of comorbidities recorded according to the International Classification of Diseases 9 codes
Measured: Through study completion , an average of 5 years
Treatment-Emergent comorbidities
Incidence of comorbidities emerging in patients exposed to specific treatments
Measured: Through study completion , an average of 5 years
Treatment efficacy
Hours of presence of angioedema symptoms during specific long term prophylaxis
Measured: Through study completion , an average of 5 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted4 Feb 2019
- Study start1 Oct 2017
- Primary completion31 Dec 2019 (estimated)
- Study completion31 Dec 2023 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Hereditary Angioedema Type I and IIStudies 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
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 220 participants (estimated)
- Target duration
- 1 Year
Sponsor and investigators
- Lead sponsor
- HAE Global Registry Foundation
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- marco cicardi, MD, Principal investigator, HAE Global Registry Foundation
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03828279
- Sponsor's protocol ID
- HAERegistry
- Acronym
- HGR
- Status last verified
- Jan 2019
- First submitted
- 23 Jan 2019
- Last updated
- 5 Feb 2019
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: All registry members, as single or group, can propose studies based on aggregated anonymized data by addressing the request to the HAE Global Registry Scientific Committee (HGRSC)
Study at a glance
From the registry record, last updated by the sponsor on 5 Feb 2019. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Global Registry on Hereditary Angioedema Type I and II
- ClinicalTrials.gov ID
- NCT03828279
- Acronym / sponsor ID
- HGR / HAERegistry
- Conditions
- Hereditary Angioedema Type I and II
- Keywords
- angioedema, disease registry, C1 inhibitor, anti bradykinin treatments
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 220 participants (estimated)
- Lead sponsor
- HAE Global Registry FoundationUniversity, hospital or other
- Study start
- 1 Oct 2017 (actual)
- Primary completion
- 31 Dec 2019 (estimated)
- Study completion
- 31 Dec 2023 (estimated)
- First posted
- 4 Feb 2019 (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.
The objective of this international hereditary angioedema (HAE) register is to collect homogeneous clinical and laboratory data on patients with HAE type I and II gathering better information on the natural course of the disease and detecting therapeutic options to manage it.
Detailed description
It is an international multicenter disease registry, the principal investigator at each center is responsible for competent ethic committee/institutional review board approval and for identifying co-investigators, who collect patients' informed consent and insert patients' data. Participating patients own their data. Upon acceptance of the informed consent, the treating physician transfers data of the case report form (CRF) to a specifically designed electronic support (eCRF) and the patients enter data on attacks. Physicians at center fill-in the eCRF with data for demography, diagnosis, prophylaxis and associated diseases. Plasma levels of C1 inhibitor antigen and function and of C4 antigen document laboratory diagnostic criteria. Each patient has a national identifier code. Patients fill-in attack reports that encompass duration, severity and treatment of each angioedema episode. C1 inhibitor coding gene (SERPING1) genotype is entered according to the last Hugo nomenclature. Yearly update of information is recommended, patients with follow up above two years are moved in a separate area and excluded from analysis. Each patient prospectively fills data on attacks. On a specific informed consent, the patient can agree on storing biological material (plasma and nucleic acids) for research purposes.
The data processor is an innovative start-up (Cloud-R s.r.l. Milan, Italy) that manages all data according to a specific contract and in compliance with current regulation on sensitive data security and processing. The Registry, delivered in the mode of Registry-as-a-Service (RaaS), is designed following General Data Protection Regulation (GDPR) guidelines, and issues regular software and infrastructure enhancements as a part of the normal operational mode. The system generates statistics of aggregated anonymized data following the participating centers' hierarchy levels and Global Registry governance rules. Patients supply data on attacks either on paper support or using a Web form or a mobile application. These data will flow into a staging area for physician validation before being considered valid for statistics. For each entry the system updates in real-time all the statistics and dashboards. The platform has configurable functionalities to support data quality management. It provides data format validation, integration to external qualified libraries, alerts, dashboards, automatic index calculations, advanced filters and queries, data change log. This open architecture, allows integration of the system, via standard API's, to external or sub-registries, registries, biobanks and clinical bioinformatics tools, i.e. for specific trial studies leveraging a specific cluster of patients already present in the Global Registry.
An independent non-profit foundation (HGRF) made of representatives of patients' associations is in charge for funding and delegates all the management to the HAE Global Registry Board (HGRB). The HGRB is in charge for operational, assisted by the HAE Global Registry Scientific Committee (HGRSC) for topics of competence. No registry member, center, group or board can access the entire set of data. All registry members, as single or group, can propose studies based on aggregated data by addressing the request to the HGRSC. Analysis and studies of data at local centers can occur at any time. Members of HGRB and HGRSC are elected to be representative of different cultural and geographic backgrounds. Their offices have a two-year term with no more than one consecutive renewal. Angioedema centers can join the Registry upon request to the HGRB . The registry quality control system periodically checks Registry entries and compliance of eCRF with the source data. For each information, the system will grant traceability of time and author.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Target follow-up
- 1 Year
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| hereditary angioedema type I | – | Diagnostic Test: functional and antigenic C1 inhibitorPatients were diagnosed as C1 inhibitor HAE type I when functional and antigenic C1 inhibitor were ≤ 50% of normal |
| hereditary angioedema type II | – | Diagnostic Test: functional and antigenic C1 inhibitorPatients were diagnosed as type II when functional C1 inhibitor was ≤50% and antigenic was >50% of normal |
Who may qualify
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult, Older adult
- Study population
- patients diagnosed with HAE type I and II and followed by a referral center for angioedema
Key inclusion criteria (2 listed)
- patients diagnosed with HAE type I and II with signed informed consent
- laboratory diagnostic criteria documenting plasma levels of C1 inhibitor antigen and function and of C4 antigen
Key exclusion criteria (3 listed)
- patients without HAE type I and II
- patients without documented laboratory diagnostic criteria
- patients not capable to give informed consent
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 |
|---|---|---|
| functional and antigenic C1 inhibitorAlso: genetic analysisDiagnosis of HAE is based on personal and/or family history of angioedema and on C1 inhibitor functional or antigenic plasma levels ≤50% of normal. | Diagnostic test | hereditary angioedema type I, hereditary angioedema type II |
Primary outcome
Number of angioedema events
Time frame: Through study completion, an average of 5 years
Number of angioedema events
Time of angioedema events
Time frame: Through study completion, an average of 5 years
Time in hours of presence of angioedema symptoms
Severity of angioedema events
Time frame: through study completion, an average of 5 years
Number of severe, moderate, mild angioedema symptoms based on a three point scale patient reported outcome
3 secondary outcomes
Comorbidities
Time frame: Through study completion , an average of 5 years
Treatment-Emergent comorbidities
Time frame: Through study completion , an average of 5 years
Treatment efficacy
Time frame: Through study completion , an average of 5 years
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 5 Feb 2019.
- Individual participant dataSharing planned: Yes. All registry members, as single or group, can propose studies based on aggregated anonymized data by addressing the request to the HAE Global Registry Scientific Committee (HGRSC)
Related trials for Hereditary Angioedema Type I and II
Enrolling by invitationPhase 2/3
Extension Study of Oral PHA-022121 for Acute Treatment of Angioedema Attacks in Patients With Hereditary Angioedema
Hereditary Angioedema, Hereditary Angioedema Type I
Not yet recruitingObservational study
A Study About the Diagnosis and Management of Hereditary Angioedema (HAE) in Egypt
Hereditary Angioedema (HAE)
Active, not recruitingObservational study
A Study of Lanadelumab in Teenagers and Adults With Hereditary Angioedema (HAE)
Hereditary Angioedema (HAE)
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. This study is not recruiting at the moment.
marco cicardi, MD principal investigator
HAE Global Registry Foundation
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Hereditary Angioedema Type I and II, run by HAE Global Registry Foundation at 1 site in Italy.
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 2 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: status not confirmed, as of the sponsor's last update on 5 Feb 2019. 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 Italy. 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?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact marco cicardi, MD (+39 0239042516, marco.cicardi@unimi.it), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Number of angioedema events (time frame: Through study completion, an average of 5 years). The study lists 3 primary outcomes in all. 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 5 Feb 2019.