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: 2025-12-24 @ 9:07 PM
Ignite Modification Date: 2025-12-24 @ 9:07 PM
NCT ID: NCT06439004
Eligibility Criteria: Inclusion Criteria: * Voluntary written informed consent has been obtained prior to any screening procedures. * Subject is ≥ 18 years and ≤ 25 years of age. * Subject is a non-smoker for at least 6 months before the start of the study. * Subject has a body mass index (BMI) between 18-30 kg/m². * Subject is in good general health, based on medical history and vital signs. Exclusion Criteria: * Subject has a history of any illness which, in the investigator's opinion, might confound the results of the study, including conditions which affect the normal somatosensory functionality. * Subject has eczema, scleroderma, psoriasis, dermatitis, or any other abnormality on the skin of the dominant hand, right forearm, right flank or lower back which, in the investigator's opinion, might interfere with the study assessments. * Subject is unable to refrain from drinking alcohol 24 hours prior to each study visit, is currently a user of drugs, or has a history of alcohol and/or drug abuse. * Subject is unable to refrain from drinking caffeinated beverages 24 hours prior to each study visit. * Subject has used concomitant drugs and/or treatments that may interfere, in the investigator's opinion, with the study results. * Subject is in a situation or has a condition which, in the investigator's opinion, may interfere with safe and optimal participation in the study. * Female subject who is pregnant, breast-feeding or intends to become pregnant or is of child-bearing potential and is not using an adequate contraceptive method. * Subject is participating in another trial which, in the investigator's opinion, might confound the results of the study.
Healthy Volunteers: True
Sex: ALL
Minimum Age: 18 Years
Maximum Age: 25 Years
Study: NCT06439004
Study Brief:
Protocol Section: NCT06439004