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 @ 11:57 PM
Ignite Modification Date:
2025-12-24 @ 11:57 PM
NCT ID:
NCT05526651
Eligibility Criteria:
Inclusion Criteria:
* subject who had urinary retention 6 hours after vaginal delivery and the residual urine volume 500 - 1000 mL
* female 20 - 40 years old
* pregnancy \> 34 weeks and baby's weight \> 2000 gr
* agree to participate in this study and sign the inform consent
Exclusion Criteria:
* patient who had emergency situation, such as bleeding or unstable hemodynamic
* using pace maker
* had cardiac arrhythmia
* patient had disease that make them using the catheter (such as chronic kidney disease)
* allergy to stainless steel
* scar in the acupuncture point locations
* using prothesis
* had intrathecal labour analgesia (ILA)
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
20 Years
Maximum Age:
40 Years
Study:
NCT05526651
Study Brief:
Protocol Section:
NCT05526651