Trial · NCT02542748
Comparison of Norepinephrine and Ephedrine on Hypotension After Spinal Anesthesia in Parturients
NCT02542748, Not applicable, Completed, Air Force Military Medical University, China
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Comparison of Norepinephrine and Ephedrine on Hypotension After Spinal Anesthesia in Parturients. Trials, record NCT02542748. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02542748
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Comparison of Norepinephrine and Ephedrine on Hypotension After Spinal Anesthesia in Parturients
- NCT number
- NCT02542748
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 66 participants, actual
- Lead sponsor
- Air Force Military Medical University, China
- Conditions
- Hypotension, Obstetrical Complication of Anesthesia, Complications; Cesarean Section
- Interventions
- Norepinephrine, Ephedrine
- First posted
- 2015-09-07
- Last updated
- 2019-01-15
Source ClinicalTrials.gov
Registered outcomes14
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | incidence of hypotension | from immediately after spinal anesthesia to 30min after spinal anesthesia | |
| Secondary | pH value of fetal arterial blood | just after clamp of the umbilical cord, usually 1min to 10min after start of the surgery | |
| Secondary | incidence of nausea and vomiting | from immediately after spinal anesthesia to 30min after spinal anesthesia | |
| Secondary | incidence of dizzy | from immediately after spinal anesthesia to 30min after spinal anesthesia | |
| Secondary | incidence of chest congestion | from immediately after spinal anesthesia to 30min after spinal anesthesia | |
| Secondary | fetal arterial partial pressure of oxygen | just after clamp of the umbilical cord, usually 1min to 10min after start of the surgery | |
| Secondary | arterial base excess of fetal arterial blood | just after clamp of the umbilical cord, usually 1min to 10min after start of the surgery | |
| Secondary | lowest neonatal cerebral oxygen saturation | from clamp of the umbilical cord to 10 min later, 10min in total | |
| Secondary | lactate level of fetal arterial blood | just after clamp of the umbilical cord, usually 1min to 10min after start of the surgery | |
| Secondary | number of rescue vasoactive agent | from immediately after spinal anesthesia to 30min after spinal anesthesia |
1 to 10 of 14Source ClinicalTrials.gov
See all 14 registered outcomesOutcomes0
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.
Papers4
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/NCT02542748
GET https://conductscience.org/api/trials/v1/NCT02542748/registered