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 @ 3:51 PM
Ignite Modification Date:
2025-12-24 @ 3:51 PM
NCT ID:
NCT05475392
Eligibility Criteria:
Inclusion Criteria:
* Women of age from 25 to 35years,
* All patients must be in breastfeeding period at least 6 weeks after delivery,
* BMI of women must be less than 30 kg/m²,
* Parity of women must not more than 3 times
Exclusion Criteria:
* Patient should not be in Pregnancy phase.
* There should not be Positive neurological examination
* Cervical spine surgery or stenosis patients should not be included
* Metastases patients should not be included.
* Participants should not have aassociated pathology of the upper cervical region or upper limb that may cause overlapping with the clinical finding as referred pain from costotransverse joint, rotator cuff tendonitis, and cervical rib syndrome
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
25 Years
Maximum Age:
35 Years
Study:
NCT05475392
Study Brief:
Protocol Section:
NCT05475392