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NCT02902172 · ClinicalTrials.gov registry record · Phase 4
NSAID Use in Postpartum Hypertensive Women
A Phase 4 study, sponsored by St. Louis University.
- Terminated
- Registry status
- Phase 4
- Development phase
- 36
- Enrollment target
NCT02902172 is a Phase 4 study that was terminated before completion, run by St. Louis University. The registered enrollment target is 36 participants.
The verdict
NCT02902172, a Phase 4 study, was terminated before completion, sponsored by St. Louis University.
- TERMINATED
- Registry status
- Phase 4
- Development phase
- 36 participants
- Enrollment target
Study Summary
Women who have the diagnosis of hypertension (pre-pregnancy and pregnancy induced) and deliver an infant via vaginal delivery will be placed into two groups in the postpartum period. One group will receive Ibuprofen for pain control and the other group will be given Tylenol. Blood pressures during the postpartum period will then be collected and compared in order to see if NSAIDs use increases blood pressure.
Interventions
- DRUG Acetaminophen
- DRUG NSAID
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 36 participants |
| Start Date | 2017-03-15 |
| Est. Completion | 2017-10-08 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02902172
The ClinicalTrials.gov registry entry for NCT02902172 describes a study currently listed as terminated, categorized as Phase 4. The registered enrollment target is 36 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is St. Louis University, which has 107 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Acetaminophen is the first listed.
NCT02902172 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02902172 about?
NCT02902172 is a clinical study titled "NSAID Use in Postpartum Hypertensive Women". Women who have the diagnosis of hypertension (pre-pregnancy and pregnancy induced) and deliver an infant via vaginal delivery will be placed into two groups in the postpartum period. One group will receive Ibuprofen for pain control and the other group will be given Tylenol. Blood pressures during t...
What is the current status of trial NCT02902172?
This trial is currently terminated. It is a Phase 4 study. The enrollment target is 36 participants. The study started on 2017-03-15. Estimated completion is 2017-10-08.
What interventions are being tested in trial NCT02902172?
The interventions under investigation include: Acetaminophen (DRUG), NSAID (DRUG).
Who is sponsoring clinical trial NCT02902172?
This trial is sponsored by St. Louis University, which has 107 total clinical trials registered on ClinicalTrials.gov.
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