Trial · NCT07513870
Registered outcomes11
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
1 to 11 of 11
Download this page as JSON| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Depth 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 |
| Primary | Neonatal 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 |
| Secondary | Umbilical Cord Arterial pH | within the first 5 minutes after delivery | Analysis of umbilical cord blood evaluating pH, to assess the newborn's immediate postnatal transition and metabolic state. |
| Secondary | Umbilical Cord Arterial pco2 | Within the first 5 minutes after delivery | Analysis of umbilical cord blood evaluating PCO2, to assess the newborn's immediate postnatal transition and metabolic state. |
| Secondary | Umbilical Cord Arterial po2 | Within the first 5 minutes after delivery | Analysis of umbilical cord blood evaluating PO2, to assess the newborn's immediate postnatal transition and metabolic state. |
| Secondary | Umbilical Cord total hemoglobin | Within the first 5 minutes after delivery | Analysis of umbilical cord blood evaluating total hemoglobin, to assess the newborn's immediate postnatal transition and metabolic state. |
| Secondary | Umbilical Cord glucose levels | Within the first 5 minutes after delivery | Analysis of umbilical cord blood evaluating glucose levels, to assess the newborn's immediate postnatal transition and metabolic state |
| Secondary | Maternal 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. |
| Secondary | Maternal 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. |
| Secondary | Maternal 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. |
| Secondary | Maternal Heart Rate | Intraoperative (Recorded from induction to the end of the operation) | Continuous monitoring of heart rate to assess maternal cardiovascular stability. |
Source ClinicalTrials.govtrials-2026-11-12-0.5.0
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 list from software.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/trials/v1/NCT07513870/registered