Trial · NCT04370847
Ultrasonography for Fluid Assessment in Parturients With Preeclampsia Undergoing Cesarean Section
NCT04370847, Completed, Mansoura University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Ultrasonography for Fluid Assessment in Parturients With Preeclampsia Undergoing Cesarean Section. Trials, record NCT04370847. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04370847
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Ultrasonography for Fluid Assessment in Parturients With Preeclampsia Undergoing Cesarean Section
- NCT number
- NCT04370847
- Status
- Completed
- Enrollment
- 100 participants, actual
- Lead sponsor
- Mansoura University
- Conditions
- Elective Cesarean Section, Preeclampsia
- Interventions
Spinal Anesthesia, Intrathecal Bupivacaine, Intrathecal Fentanyl, Cesarean Delivery, lung ultrasound scans, Ultrasound Assessment of the Inferior Vena Cava, Optic nerve sheath diameter, ringer acetate, Intravenous Ephedrine, Intravenous Syntocinon
- First posted
- 2020-05-01
- Last updated
- 2024-11-13
Source ClinicalTrials.gov
Registered outcomes10
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Ultrasonographic fluid assessment | Time frame:preoperative(baseline) and 2 hours after spinal anesthesia. | Detection of change in overall number of B lines (ECS) by lung ultrasound |
| Secondary | Urine output | For 2 hours after spinal anesthesia | total urine output at 2 hours after spinal anesthesia |
| Secondary | Oliguria | For 2 hours after spinal anesthesia | Incidence of oliguria defined as a total urine output \<60 mL/hr |
| Secondary | Ephedrine use | Intraoperative | total ephedrine dose |
| Secondary | Intraoperative bradycardia | Intraoperative | Incidence of bradycardia (Heart rate \<50 beats/minute) |
| Secondary | Incidence of nausea and vomiting. | Intraoperative | Incidence of nausea and/or vomiting as reported by the patient |
| Secondary | Difference between overall number of b lines | baseline and 1hour post spinal | difference between overall number of b lines preoperative(baseline) and at 1 hour after spinal anesthesia. |
| Secondary | Inferior Vena Caval Diameters | Baseline, and at 1 and 2 hours post-spinal | Maximum, minimum inferior vena cava diameters and inferior vena cava collapsibility index changes over time. |
| Secondary | Difference between optic nerve sheath diameter | baseline,at 1hour and at 2 hours of spinal anesthesia. | optic nerve sheath diameter changes over time. |
| Secondary | Neonatal Apgar score | 5 min after delivery | neonatal Apgar score to assess neonatal wellbeing at 5 min after 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/NCT04370847
GET https://conductscience.org/api/trials/v1/NCT04370847/registered