ConductScience.org, home

Trial · NCT07513870

Comparing Inhalational Anesthesia and TIVA on Maternal and Neonatal Hemodynamics in Elective Cesarean Section

NCT07513870, Not applicable, Completed, Medipol University

3 sourcestrials-2026-11-12-0.5.0

Download JSON
Cite this record

ConductScience Library. Comparing Inhalational Anesthesia and TIVA on Maternal and Neonatal Hemodynamics in Elective Cesarean Section. Trials, record NCT07513870. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07513870

On this page

Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Comparing Inhalational Anesthesia and TIVA on Maternal and Neonatal Hemodynamics in Elective Cesarean Section
NCT number
NCT07513870
Status
Completed
Phases
Not applicable
Enrollment
80 participants, actual
Lead sponsor
Medipol University
Conditions
Cesarean Section, Anesthesia, General, Anesthesia, Intravenous
Interventions
Propofol, Sevoflurane
First posted
2026-04-07
Last updated
2026-04-07

Source ClinicalTrials.gov

Registered outcomes11

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryDepth of Anesthesia Assessed by Bispectral Index (BIS)During surgery (at 1, 2, 5, 10, 20, 30, 40 minutes and at the end of surgery)
Anesthesia depth was monitored continuously using a four-channel frontal pEEG electrode to maintain a target BIS value between 40 and 55. The Bispectral Index scale ranges from a minimum of 0 to a maximum of 100. Lower scores indicate deeper sedation/anesthesia, while higher scores indicate a more awake state
PrimaryNeonatal Neurologic and Adaptive Capacity Score (NACS)At 1 minute, 1 hour, and 24 hours post-delivery
The Neonatal Neurologic and Adaptive Capacity Score (NACS) is a neurobehavioral assessment scale for newborns. The scale ranges from a minimum score of 0 to a maximum score of 40. Higher scores indicate a better outcome (better neurological adaptation). Scores of 35 or above indicate normal/adequate neurological adaptation, while scores below 35 indicate inadequate adaptation
SecondaryUmbilical Cord Arterial pHwithin the first 5 minutes after deliveryAnalysis of umbilical cord blood evaluating pH, to assess the newborn's immediate postnatal transition and metabolic state.
SecondaryUmbilical Cord Arterial pco2Within the first 5 minutes after deliveryAnalysis of umbilical cord blood evaluating PCO2, to assess the newborn's immediate postnatal transition and metabolic state.
SecondaryUmbilical Cord Arterial po2Within the first 5 minutes after deliveryAnalysis of umbilical cord blood evaluating PO2, to assess the newborn's immediate postnatal transition and metabolic state.
SecondaryUmbilical Cord total hemoglobinWithin the first 5 minutes after deliveryAnalysis of umbilical cord blood evaluating total hemoglobin, to assess the newborn's immediate postnatal transition and metabolic state.
SecondaryUmbilical Cord glucose levelsWithin the first 5 minutes after deliveryAnalysis of umbilical cord blood evaluating glucose levels, to assess the newborn's immediate postnatal transition and metabolic state
SecondaryMaternal Systolic Blood Pressure (Unit: mmHg)Intraoperative (Recorded from induction to the end of the operation)Continuous monitoring of systolic arterial blood pressures to assess maternal cardiovascular stability.
SecondaryMaternal diastolic Blood Pressure (Unit: mmHg)Intraoperative (Recorded from induction to the end of the operation)Continuous monitoring of diastolic arterial blood pressures, to assess maternal cardiovascular stability.
SecondaryMaternal mean Blood Pressure (Unit: mmHg)Intraoperative (Recorded from induction to the end of the operation)Continuous monitoring of mean arterial blood pressures, to assess maternal cardiovascular stability.

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.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

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/NCT07513870

GET https://conductscience.org/api/trials/v1/NCT07513870/registered