Acupuncture Point P6 Stimulation for Reduction of Nausea and Vomiting During Cesarean
Completed · Phase 4
Conditions studied: Nausea, Vomiting, Satisfaction
In brief
The purpose of this study is to compare the effectiveness of acupressure point P6 stimulation versus intravenous ondansetron plus metoclopramide versus no antiemetic prophylaxis during elective cesarean section under regional anesthesia.
Key facts
- Study ID
- NCT02959840
- Run by
- Rutgers, The State University of New Jersey
- People needed
- 180
- Starts
- 2015-07-01
- Expected to finish
- 2017-08-23
- Last updated by the study team
- 2017-09-25
Who can join
Age: 18 and older, up to 45. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- Female subjects ages 18 to 45
- Subjects with American Society of Anesthesiologists (ASA) Class I or II
- Subjects with elective primary or repeat cesarean delivery
- Subjects who receive combined spinal epidural anesthesia
- English and non-English speaking subjects will be included in the study
You may not qualify if…
- Female subjects <18 years of age
- Subjects requiring emergent cesarean delivery
- History of placenta accrete
- Multiple gestation pregnancy
- ASA status III or higher
- Current history of pregnancy induced hypertension, pre-eclampsia, or eclampsia
- History of any chronic medication use (other than prenatal vitamins), including inhaler medications
- Current urinary tract infection, pneumonia, or otitis media
Where it is running
- Robert Wood Johnson University Hospital — New Brunswick, New Jersey, United States
Full record on ClinicalTrials.gov
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