Trial · NCT03978767
Preeclampsia And Nonsteroidal Drugs for Analgesia: a Randomized Non Inferiority Trial
NCT03978767, Phase 2, Completed, Washington University School of Medicine
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Preeclampsia And Nonsteroidal Drugs for Analgesia: a Randomized Non Inferiority Trial. Trials, record NCT03978767. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03978767
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Preeclampsia And Nonsteroidal Drugs for Analgesia: a Randomized Non Inferiority Trial
- NCT number
- NCT03978767
- Status
- Completed
- Phases
- Phase 2
- Enrollment
- 287 participants, actual
- Lead sponsor
- Washington University School of Medicine
- Conditions
- Preeclampsia Severe, Preeclampsia Postpartum
- Interventions
- Ibuprofen 600 mg, Ketorolac, Acetaminophen, Oxycodone
- First posted
- 2019-06-07
- Last updated
- 2026-06-22
Source ClinicalTrials.gov
Registered outcomes7
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | postpartum antihypertensive requirements | at the end of hospitalization, up to 7 days after randomization | measurement of anti-hypertensive requirements at time of discharge |
| Secondary | Postpartum pain scores | From randomization to 6 weeks after randomization | Evaluate the effect of NSAIDs on patient perception of pain |
| Secondary | Postpartum opioid use | From randomization to 6 weeks after randomization | Compare the opioid requirements in each arm |
| Secondary | Mean arterial blood pressure | From randomization to 6 weeks after randomization | Compare peak, average and median MAPs postpartum |
| Secondary | End organ damage | during hospitalization, an average of 4 days | Evaluate for evidence of renal, hepatic or neurological injury in the poatpartum period |
| Secondary | Hospital readmission | From randomization to 6 weeks after randomization | Evaluate the incidence of hospital readmission rate postpartum |
| Secondary | Continued anti-hypertensive requirement | up to 6 weeks | evaluate the need for antihypertensive medications at 6 weeks postpartum |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers5
The papers the trial lists on ClinicalTrials.gov.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT03978767
GET https://conductscience.org/api/trials/v1/NCT03978767/registered