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 @ 7:35 PM
Ignite Modification Date:
2025-12-24 @ 7:35 PM
NCT ID:
NCT05338203
Eligibility Criteria:
Inclusion Criteria of Experiment Group:
* If pregnant, being in the second trimester of pregnancy; have given birth, postpartum 16th day or more
* If pregnant, not having a risky pregnancy
* If she is pregnant, there is a report from the obstetrician she is followed that there is no harm in breastfeeding
* The older child being breastfed is under the age of 2
* Absence of literacy problems, mental disabilities and communication problems
* Absence of chronic disease
* No communicable disease
* Not using a drug continuously
* Not using any medication in the last 24 hours
* Willingness to participate in the study
Inclusion Criteria of Control Group:
* Postpartum 16th day and above
* No risky pregnancy in her last pregnancy
* Being multiparous
* Absence of literacy problems, mental disabilities and communication problems
* Absence of chronic disease
* No communicable disease
* Not using a drug continuously
* Not using any medication in the last 24 hours
* Willingness to participate in the study
Exclusion criteria. During the research process, mothers will be excluded from the sample in case the mothers want to leave the study, the sample milk is spoiled or there are losses during the analysis.
Healthy Volunteers:
True
Sex:
FEMALE
Study:
NCT05338203
Study Brief:
Protocol Section:
NCT05338203