Trial · NCT07893808
Anesthesia and Neonatal Outcomes After Cesarean Delivery
NCT07893808, Completed, Serra Topal
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Anesthesia and Neonatal Outcomes After Cesarean Delivery. Trials, record NCT07893808. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07893808
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Anesthesia and Neonatal Outcomes After Cesarean Delivery
- NCT number
- NCT07893808
- Status
- Completed
- Enrollment
- 21,926 participants, actual
- Lead sponsor
- Serra Topal
- Conditions
- Cesarean Delivery
- Interventions
- General Anesthesia (GA), Neuraxial Anesthesia (NA)
- First posted
- 2026-10-26
- Last updated
- 2026-10-26
Source ClinicalTrials.gov
Registered outcomes7
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Incidence of 5-Minute Apgar Score Below 7 | 5 minutes after birth | Proportion of live-born neonates with an Apgar score below 7 at 5 minutes after birth, compared between general and neuraxial anesthesia groups and evaluated separately for elective and emergency cesarean deliveries. |
| Secondary | Incidence of 1-Minute Apgar Score Below 7 | 1 minute after birth | Proportion of live-born neonates with an Apgar score below 7 at 1 minute after birth, compared between general and neuraxial anesthesia groups and evaluated separately for elective and emergency cesarean deliveries. |
| Secondary | NICU Admission Within 24 Hours After Birth | Up to 24 hours after birth | Proportion of neonates admitted to the study hospital's neonatal intensive care unit (NICU) or transferred to an external NICU within 24 hours after birth. Transfers to external NICUs were included in this outcome. |
| Secondary | Admission to a Level III Neonatal Intensive Care Unit | From birth to NICU discharge, up to 174 days | Proportion of neonates admitted to a Level III NICU during an admission initiated within 24 hours after birth. This outcome was assessed only for infants who remained at the study hospital because post-transfer information from external hospitals was unavailable. |
| Secondary | Invasive Ventilation During NICU Admission | From birth to NICU discharge, up to 174 days | Proportion of neonates with tracheal intubation or mechanical ventilation recorded during a NICU admission that began within 24 hours after birth. This outcome was assessed only for infants who remained at the study hospital. The timing of ventilation within the admission was not recorded. |
| Secondary | Non-Invasive Ventilation During NICU Admission | From birth to NICU discharge, up to 174 days | Proportion of neonates receiving non-invasive ventilation during a NICU admission that began within 24 hours after birth. Only infants who remained at the study hospital were included because post-transfer information was unavailable. The timing of ventilation within the admission was not recorded. |
| Secondary | Length of Neonatal Intensive Care Unit Stay | From birth to NICU discharge, up to 174 days | Duration of NICU stay, measured in days, among neonates admitted to the study hospital's NICU. Infants transferred to external hospitals were excluded because complete post-transfer hospitalization data were unavailable. |
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/NCT07893808
GET https://conductscience.org/api/trials/v1/NCT07893808/registered