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 @ 2:04 AM
Ignite Modification Date:
2025-12-25 @ 2:04 AM
NCT ID:
NCT02532660
Eligibility Criteria:
Inclusion Criteria:
* Subjects from both sexes aged between 18 and 65 years;
* Patient diagnosed with mild depression episode confirmed by psychiatric and psychometric evaluation, presenting basal scores above 08 and below 24 measured by the Hamilton Rating Scale (HAM-D);
* Capable of understanding the nature and objective of the study, including risks and adverse effects and intended to cooperate with the researcher and act in accordance with the requirements of the entire protocol, which comes to be confirmed by signing the informed consent.
Exclusion Criteria:
* Have a known hypersensitivity to Trichilia catigua or history of serious adverse reactions;
* Shows risk of suicide, assault, murder or moral exposure;
* Clinical history of bleeding disorders;
* Drug addiction, including alcohol;
* Known or suspected neoplasia;
* Knowledge positive test result for the human immunodeficiency virus;
* Patient not willing to adhere to the procedures of the Protocol;
* For women, can not be pregnant or nursing and must be in use of a contraception method during the participation in the study;
* Patients using other drugs with sedative or antidepressant action, which can not be suspended for 15 days (wash out);
* Diabetics;
* Hyperthyroidism;
* Participation in any experimental study or use of any experimental drug three months before the start of this study;
* Has any condition which the investigator deems relevant to the non-participation of the study.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
65 Years
Study:
NCT02532660
Study Brief:
Protocol Section:
NCT02532660