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Trial · NCT07899216

Registered outcomes11

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

ListOutcomeTime frameDescription
PrimaryThe incidence of maternal hypotension from initiation of spinal anaesthesia until end of the opertation .60 min after the block
The number of patients who develop hypotension (defined as decreased SBP less than 80% of the baseline reading during the period from intrathecal injection till delivery of the fetus) after spinal block divided by the total number in the group
Secondary1-Number of hypotensive episodes60 min after the blockThe number of hypotensive episode experienced by each patient in each group
Secondary2-Number of rescue vasopressor boluses required60 min after the blockNumber or rescue doses administrated to each patient when experiencing hypotension defined as SBP less than 80% of the baseline reading
Secondary3-Incidence of hypertension60 min after the blocknumber of patients who develop intraoperive hypertension (defined as increased systolic blood pressure by more than 20% of the baseline reading) divided by the total number of patients in the group
Secondary4-Incidence of maternal bradycardia, defined as HR <50 beats/min60 min after the blocknumber of patients who developed bradycardia, defined as HR \<50 beats/min
Secondary5-Incidence of nausea and vomiting60 in after the blocknumber of patients who developed nausea and vomiting
Secondary6-Incidence of shivering60 in after the blocknumber of patients who developed shivering
Secondary7- Any other maternal complications60 min after the blockany other maternal complications will be spotted and recorded
Secondary8-Apgar score1 and 5 minutes after the delivery of the babyAPGAR score for detection of the well being of the neonate
Secondary9-Umbilical arterial pH.1 min after the deliveryPH of the blood sample withdrawn from the umbilical cord
Secondary10-Umbilical arterial PaCO₂.1 min after the deliveryPaCO2 of the blood sample withdrawn from the umbilical cord

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.

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GET https://conductscience.org/api/trials/v1/NCT07899216/registered