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 @ 3:10 AM
Ignite Modification Date:
2025-12-25 @ 3:10 AM
NCT ID:
NCT00595205
Eligibility Criteria:
Inclusion Criteria:
A child's clinical episode will be defined as an IS case and deemed eligible for the study if he/she meets the following criteria:
* Subject is an IMSS affiliate
* Subject is being treated/has been treated/has been referred for treatment at one of the IMSS hospitals/medical facilities with IS during the study period.
* Male or female child is \<one year of age at the time of diagnosis of the IS (child becomes ineligible on the day of their first birthday)
* Subject is diagnosed with definite IS based on the Brighton criteria
* Written informed consent is obtained from the parent/guardian/legal representative of the subject Subjects meeting the above criteria will be eligible for inclusion in this study regardless of whether or not the subject has had a radiographically or surgically confirmed case of IS prior to the current episode.
Exclusion Criteria:
Not applicable
Healthy Volunteers:
False
Sex:
ALL
Maximum Age:
364 Days
Study:
NCT00595205
Study Brief:
Protocol Section:
NCT00595205