Trial · NCT03325348
Oral Nifedipine Versus IV Labetalol in Severe Pre Eclampsia
NCT03325348, Phase 2, Phase 3, Unknown, Services Institute of Medical Sciences, Pakistan
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Oral Nifedipine Versus IV Labetalol in Severe Pre Eclampsia. Trials, record NCT03325348. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03325348
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Oral Nifedipine Versus IV Labetalol in Severe Pre Eclampsia
- NCT number
- NCT03325348
- Status
- Unknown
- Phases
- Phase 2, Phase 3
- Enrollment
- 194 participants, estimated
- Lead sponsor
- Services Institute of Medical Sciences, Pakistan
- Conditions
- Severe Pre-Eclampsia, Antepartum
- Interventions
- Nifedipine 10 mg, Labetalol
- First posted
- 2017-10-30
- Last updated
- 2017-10-30
Source ClinicalTrials.gov
Registered outcomes4
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Time taken for Blood Pressure control | 60 minutes | Time taken to control Blood pressure will be measured |
| Secondary | Fetal distress | Labour | Fetal distress will be measured by abnormalities of fetal heart rate of fetus or passage of meconium. of Meconium |
| Secondary | Neonatal Intensive Care Unit admission, | From Birth till 7 days | If neonate needs Neonatal Intensive Care Unit admission for more than 12 hours |
| Secondary | perinatal death | From birth to 7 days | If death of baby occurs in utero or within 7 days of delivery |
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.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
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/NCT03325348
GET https://conductscience.org/api/trials/v1/NCT03325348/registered