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 @ 5:19 PM
Ignite Modification Date:
2025-12-24 @ 5:19 PM
NCT ID:
NCT05737550
Eligibility Criteria:
Inclusion Criteria:
* Signed Informed Consent Form
* Male and female
* A recurrent visitor at Sprututbytesprogrammet in Uppsala defined as visited the clinic within the last three (3) months
* SUD in accordanve with DSM-5 criteria according to investigator/designee judgement
* Age 18 and above
* Negative urine pregnancy test for all fertile women
* Been informed of the nature, the scope, and the relevance of the clinical investigation
* Voluntarily agreed on participation and has duly singed the Informed Consent Form
Exclusion Criteria:
* Participating in another clinical investigation which may affect the study outcome according to clinical judgement
* Pregnancy or lactating
* Blind
* Deaf
* Any ECG dangerous arrythmia according to the investigator or designee judgement
* Any disease or condition that may influence pupillary reflexes based on clinical judgement
* Undergone eye surgery that may influence pupillary reflexes based on clinical judgement
* Not able to read or understand the local language
* Any planned travel or treatment which will make it impossible to participate according to the investigator or designee
* Any other condition that as judged by the investigator may make the follow-up or investigation inappropriate
* That according to the Declaration of Helsinki is deemed unsuitable for study enrolment
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT05737550
Study Brief:
Protocol Section:
NCT05737550