Last updated: February 28, 2024
Sponsor: Northwestern University
Overall Status: Completed
Phase
N/A
Condition
Lactose Intolerance
Labor/delivery
Stomach Discomfort
Treatment
Magnet at P6
Magnet applied to arm not at P6 pressure point.
Clinical Study ID
NCT04799587
STU#: 00213854
Ages > 18 Female
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- ≥18 years of age
- English-speaking
- Pregnant patients presenting for scheduled cesarean delivery of a full-term fetus (>37weeks' gestation)
- Patients scheduled as ERAC
- Parturients undergoing spinal anesthesia
Exclusion
Exclusion Criteria:
- Patients requiring emergent delivery,
- Fetal demise
- Patients with adhesive allergy/sensitivity
- Patients with allergy/sensitivity to nickel,
- Patients with inability to consent,
- Patients with known abnormal placentation
- Patients with pacemakers/defibrillators
- Patients with positive COVID-19 tests
Study Design
Total Participants: 200
Treatment Group(s): 2
Primary Treatment: Magnet at P6
Phase:
Study Start date:
May 26, 2021
Estimated Completion Date:
September 30, 2023
Connect with a study center
Northwestern Memorial Hospital
Chicago, Illinois 60611
United StatesSite Not Available
Not the study for you?
Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.