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:
2026-03-26 @ 3:15 PM
Ignite Modification Date:
2026-03-26 @ 3:15 PM
NCT ID:
NCT07456592
Eligibility Criteria:
Inclusion Criteria (Aconite Poisoned Group):
* adult patients aged 18 years or above
* clinical presentations consistent with acute aconite poisoning, including neurological, gastrointestinal, or cardiovascular symptoms
* exposure to aconite alkaloids within 3 days
Exclusion Criteria (Aconite Poisoned Group):
* refusal of informed consent for urine collection
* alternative explanations for clinical presentations
Inclusion Criteria (Aconite Therapeutic Use Group):
* adult patients aged 18 years or above
* documented history of using aconite for therapeutic purposes, as prescribed by a qualified practitioner in a Chinese medicine clinic
* exposure to aconite alkaloids within 3 days
Exclusion Criteria (Aconite Therapeutic Use Group):
\- Refusal of informed consent for urine collection.
Inclusion Criteria (Control Group):
* adults aged 18 years or above
* no documented history of exposure to aconitine, benzoylaconine, or aconine within 30 days
* no clinical evidence of aconite toxicities
Exclusion Criteria (Control Group):
* refusal of informed consent for urine collection
* recent history of poisoning or overdose from any other substances within 30 days
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT07456592
Study Brief:
Protocol Section:
NCT07456592