Trial · NCT05035485
Maternal Cardiac Output Response to Rescue Norepinephrine and Phenylephrine Boluses in Patients With Severe Preeclampsia
NCT05035485, Not applicable, Completed, General Hospital of Ningxia Medical University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Maternal Cardiac Output Response to Rescue Norepinephrine and Phenylephrine Boluses in Patients With Severe Preeclampsia. Trials, record NCT05035485. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT05035485
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Maternal Cardiac Output Response to Rescue Norepinephrine and Phenylephrine Boluses in Patients With Severe Preeclampsia
- NCT number
- NCT05035485
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 40 participants, actual
- Lead sponsor
- General Hospital of Ningxia Medical University
- Conditions
- Hemodynamic Instability
- Interventions
- Phenylephrine, Norepinephrine
- First posted
- 2021-09-05
- Last updated
- 2024-02-02
Source ClinicalTrials.gov
Registered outcomes15
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Cardiac output (CO) | 1-30 minutes after spinal anesthesia. | Evaluated by the VIGILCO monitoring system. |
| Primary | Stroke volume (SV) | 1-30 minutes after spinal anesthesia | Evaluated by the VIGILCO monitoring system. |
| Primary | Systemic vascular resistance (SVR) | 1-30 minutes after spinal anesthesia | Evaluated by the VIGILCO monitoring system. |
| Secondary | Overall stability of systolic blood pressure control versus baseline | 1-30 minutes after spinal anesthesia | Evaluated by performance error (PE) |
| Secondary | Overall stability of heart rate control versus baseline | 1-30 minutes after spinal anesthesia | Evaluated by performance error (PE) |
| Secondary | The incidence of post-spinal anesthesia hypotension | 1-30 minutes after spinal anesthesia. | Systolic blood pressure (SBP) \< 80% of the baseline |
| Secondary | The incidence of severe post-spinal anesthesia hypotension. | 1-30 minutes after spinal anesthesia. | Systolic blood pressure (SBP) \< 60% of the baseline |
| Secondary | The incidence of nausea and vomiting. | 1-30 minutes after spinal anesthesia | Presence of nausea and vomiting in patients after spinal anesthesia |
| Secondary | The incidence of bradycardia. | 1-30 minutes after spinal anesthesia | Heart rate \< 60 beats/min. |
| Secondary | The incidence of hypertension. | 1-30 minutes after spinal anesthesia | Systolic blood pressure (SBP) \>120% of the baseline. |
1 to 10 of 15Source ClinicalTrials.gov
See all 15 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.
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/NCT05035485
GET https://conductscience.org/api/trials/v1/NCT05035485/registered