Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-25 @ 4:33 AM
Ignite Modification Date: 2025-12-25 @ 4:33 AM
NCT ID: NCT02567318
Eligibility Criteria: Inclusion Criteria: * Age \>18 years and \<35 years * Speak and understand Danish * Male sex * Study participants who have understood and signed the informed consent * No prescription medicine during the last 30 days. * Have participated and completed the study with the identifier: NCT02527395. Exclusion Criteria: * Study participants that cannot cooperate to the test. * Study participants who have a weekly intake of \>21 units of alcohol, or a have consumed \>3 units of alcohol within 24 hours before experimental day. * Study participants with a substance abuse, assessed by the investigator. * Study participants, who have consumed analgesics less than 3 days before experimental day. * Study participants, who have consumed antihistamines less than 48 hours before experimental day. * Study participants, who have consumed antidepressant medication during the last 30 days before experimental day. * Study participants with chronic pain. * Study participants with neurological illnesses. * Study participants with psychiatric diagnoses. * Study participants with a Body Mass Index of \>30 kg/m2 or \<18 kg/m2 * Study participants with Contraindications to MRI * Study participants that decline information regarding potential pathological findings in relation to the MRI. * Study participants that have any kind of trauma resulting in pain and administration of analgesics in the period between experimental pain testing and MRI-scan. * Study participant that experience a head trauma in the period between the experimental pain testing and the MRI-scan.
Healthy Volunteers: True
Sex: MALE
Minimum Age: 18 Years
Maximum Age: 35 Years
Study: NCT02567318
Study Brief:
Protocol Section: NCT02567318