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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03416114
Other study ID # RegistRare
Secondary ID
Status Recruiting
Phase N/A
First received January 23, 2018
Last updated January 23, 2018
Start date September 1, 2017
Est. completion date August 2027

Study information

Verified date January 2018
Source University of Florence
Contact Silvia Benemei, MD
Phone 00393452842070
Email silvia.benemei@unifi.it
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Retro-prospective survey on specific and overall prevalence and incidence of rare primary headaches (Part One, Chapter 3 and Chapter 4, ICHD-3 beta) in patients referred to Italian Tertiary Headache Centres in a 3-year (May 1, 2014-April 30, 2017 - retrospective data) and annually (from May 1, 2017 - prospective data).


Description:

We planned to collect data from May 1, 2014 and afterwards, by means of both retrospective and prospective approaches.

All patients who have received or will receive a diagnosis of rare primary headache will be asked to participate and, to this aim, to give their informed consent. Each participating Centre should have received the approval of the competent Ethics Committee before commencing any study procedures.

The registry will contain anagraphic information and data about diagnosis, treatment, comorbidity, and clinical features of the headache. Patients' data will be coded through the Italian Health System unique identifier, in order to avoid duplications of patients referring to more than one Centre and also to monitor multiple referrals.

A web-based open source platform (SurveyMonkey.org) will be used to collect data.


Recruitment information / eligibility

Status Recruiting
Enrollment 3000
Est. completion date August 2027
Est. primary completion date August 2027
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- diagnosis of rare primary headaches (Part One, Chapter 3 and Chapter 4, ICHD-3 beta)

- signed informed consent

Exclusion Criteria:

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Italy Careggi University Hospital Florence

Sponsors (7)

Lead Sponsor Collaborator
Silvia Benemei Maggiore Bellaria Hospital, Bologna, University of L'Aquila, University of Modena and Reggio Emilia, University of Naples, University of Roma La Sapienza, University of Trieste

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence and prevalence in Tertiary headache Centres 10 years
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