CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 715 enrolled
Drug / intervention
Questionnaireother
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04617808
NCT04617808N/ACompleted

Predictive Score for Non-traumatic Secondary Headache After an Emergency Call

Centre Hospitalier Régional d'Orléans·observational·Posted Nov 5, 2020·Updated Mar 28, 2022

In Brief

An observational study evaluating Questionnaire for Headache and Emergencies. Completed, enrolled 715 participants across 2 sites.

Detailed Summary

The study objective was to identify predictive criteria of severe non-traumatic secondary headache among the information gathered during telephone interview conducted by the on-call regulating physician at the Centre15.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesFrance
Collaborators--

Timeline

N/ACompletedFinished
202120222023202420252026
First PostedNov 5, 2020
Enrollment StartOct 21, 2020
Primary CompletionMay 31, 2021
TodayJul 2, 2026
Enrollment to primary: 7 monthsPosted 5.7 years ago

Interventions

Questionnaireother

The regulatory scheme applied to all investigative centers is as follows: * Call from Center 15 by a major patient for secondary headache no traumatic. (i.e. not having been the victim of a head trauma during the 48 hours preceding the call) * Detection of the pattern of "non-traumatic headache", by the regulatory assistant medical with registration of the word "cephareg" in the medical regulation software in order to alert the regulator about the possible inclusion of the patient * If possible, patient information on the collection of their data for research and possibility of opposing * Filling of a medical questionnaire by the regulating doctor * Weekly collection of medical questionnaires by investigating doctors