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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06030973
Other study ID # PROLOGUE
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date August 31, 2023
Est. completion date September 2, 2023

Study information

Verified date September 2023
Source Universitair Ziekenhuis Brussel
Contact Maarten Moens
Phone +3224775514
Email stimulusresearchgroup@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The goal of this online survey is to gain further insights in the needs and burden for a European registry for neuromodulation, according to healthcare providers.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date September 2, 2023
Est. primary completion date September 2, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Male and female adults who are involved in the management of chronic pain and more specifically in neuromodulation for pain (including but not limited to anesthesiologists, neurosurgeons, nurses). Exclusion Criteria: - Not involved in management of chronic pain through neuromodulation.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Filling in an online survey
Professionals are asked to complete questions regarding 1) the degree of current participation in a registry, 2) the need for a European registry, 3) the items that should be collected and 4) access to the European registry.

Locations

Country Name City State
Germany Congres Center Hamburg

Sponsors (2)

Lead Sponsor Collaborator
Moens Maarten Vrije Universiteit Brussel

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Healthcare providers their current degree of participation in a registry for neuromodulation. Degree of participation in a registry for neuromodulation (question). Cross-sectional evaluation during 3th Joint Congress of the INS European Chapters (e-INS 2023) in Hamburg in August-September 2023.
Primary Healthcare providers their need for a European registry. Underlying reasons on why a European registry is needed, or not needed (question). Cross-sectional evaluation during 3th Joint Congress of the INS European Chapters (e-INS 2023) in Hamburg in August-September 2023.
Primary Items that should be included in a registry for neuromodulation, according to healthcare providers. Items that should be collection within a registry, evaluated with a multiple choice question. Cross-sectional evaluation during 3th Joint Congress of the INS European Chapters (e-INS 2023) in Hamburg in August-September 2023.
Primary Access regulations to European registry for neuromodulation, according to healthcare providers. Access regulations, evaluated with a multiple choice question. Cross-sectional evaluation during 3th Joint Congress of the INS European Chapters (e-INS 2023) in Hamburg in August-September 2023.
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