Trial · NCT03743870
Spinal Anesthesia in Caesarean Section
NCT03743870, Unknown, Azienda Ospedaliera, Universitaria Policlinico Vittorio Emanuele
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Spinal Anesthesia in Caesarean Section. Trials, record NCT03743870. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03743870
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Spinal Anesthesia in Caesarean Section
- NCT number
- NCT03743870
- Status
- Unknown
- Enrollment
- 250 participants, estimated
- Lead sponsor
- Azienda Ospedaliera, Universitaria Policlinico Vittorio Emanuele
- Conditions
- Hypotension Drug-Induced, Cesarean Section Complications, Spinal Anesthetics Causing Adverse Effects in Therapeutic Use, Bradycardia
- Interventions
- Levobupivacaine, Bupivacaine
- First posted
- 2018-11-16
- Last updated
- 2021-07-21
Source ClinicalTrials.gov
Registered outcomes17
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Changes in blood pressure measured continuously by the EV1000® platform and the Clearsight® non-invasive system (Edwards Lifesciences) in the two study cohorts | From arrival in the operating room until the completion of surgical procedures | |
| Secondary | Incidence of hypotension during spinal anesthesia | At 60 minutes after completion of surgical procedures | |
| Secondary | Incidence of bradycardia during spinal anesthesia | At 60 minutes after completion of surgical procedures | |
| Secondary | Need for inotropes and / or vasopressor during surgery | At 60 minutes after completion of surgical procedures | Doses of inotropes and / or vasopressor administered during surgery |
| Secondary | Need for fluids administration during surgery | At 60 minutes after completion of surgical procedures | Volume of fluids administered during surgery for the eventual treatment of hypotension |
| Secondary | Level of the sensory block reached | At 15 minutes from the beginning of anesthesia | |
| Secondary | Time in which sensory block occurs | At 15 minutes from the beginning of anesthesia | |
| Secondary | Level of the sensory block reached | At 30 minutes from the beginning of anesthesia | |
| Secondary | Time in which sensory block occurs | At 30 minutes from the beginning of anesthesia | |
| Secondary | Level of sensory block reached | At 60 minutes from the beginning of anesthesia |
1 to 10 of 17Source ClinicalTrials.gov
See all 17 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/NCT03743870
GET https://conductscience.org/api/trials/v1/NCT03743870/registered