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NCT04799587 · ClinicalTrials.gov registry record · NA
Accupressure of P6 to Reduce Nausea During Cesarean Section
A NA study, sponsored by Northwestern University.
- Completed
- Registry status
- NA
- Development phase
- 200
- Enrollment target
NCT04799587 is a NA study that has completed, run by Northwestern University. The registered enrollment target is 200 participants.
The verdict
NCT04799587, a NA study, has completed, sponsored by Northwestern University.
- COMPLETED
- Registry status
- NA
- Development phase
- 200 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate if the addition of P6 pressure point stimulation as opposed to sham-point stimulation will decrease intraoperative and postoperative nausea and vomiting (IONV and PONV) for patients undergoing non-emergent cesarean delivery. We hypothesize that the addition of stimulation of the P6 pressure point to our institutional current standard of care (phenylephrine infusion, intravenous fluid bolus, and as needed intraoperative ondansetron) will decrease the occurrence of intraoperative emesis.
Interventions
- OTHER Magnet at P6
- OTHER Magnet applied to arm not at P6 pressure point.
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 200 participants |
| Start Date | 2021-05-26 |
| Est. Completion | 2023-09-30 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04799587
The ClinicalTrials.gov registry entry for NCT04799587 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 200 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Northwestern University, which has 1,209 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Magnet at P6 is the first listed.
NCT04799587 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT04799587 about?
NCT04799587 is a clinical study titled "Accupressure of P6 to Reduce Nausea During Cesarean Section". The purpose of this study is to evaluate if the addition of P6 pressure point stimulation as opposed to sham-point stimulation will decrease intraoperative and postoperative nausea and vomiting (IONV and PONV) for patients undergoing non-emergent cesarean delivery. We hypothesize that the addition o...
What is the current status of trial NCT04799587?
This trial is currently completed. It is a NA study. The enrollment target is 200 participants. The study started on 2021-05-26. Estimated completion is 2023-09-30.
What interventions are being tested in trial NCT04799587?
The interventions under investigation include: Magnet at P6 (OTHER), Magnet applied to arm not at P6 pressure point. (OTHER).
Who is sponsoring clinical trial NCT04799587?
This trial is sponsored by Northwestern University, which has 1,209 total clinical trials registered on ClinicalTrials.gov.
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