Clinical TrialID 5588

The Oxygenation of the Brain During Caesarean Section

NCT01509521

Complications; Cesarean Section

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Record Fields

Scalar fields from the final clinical_trial record.

Clinical Trial Id
5588
Evidence Id
5588
Core Evidence Id
5588
Source Clinical Trial Id
5573
Herb2 Clinical Trial Id
HBCT005573
Nct Id
NCT01509521
Title
The Oxygenation of the Brain During Caesarean Section
Status
Completed
Phase
Phase 4
Study Result
No
Study Condition
Complications; Cesarean Section
Study Type
Interventional
Study Design
Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: NONE|Primary Purpose: TREATMENT
Intervention
DRUG: Ephedrine|DRUG: Phenylephrine
Intervention Allocation
Randomized
Intervention Model
Parallel
Intervention Mask
Intervention Purpose
Treatment
Gender
Female
Age
Adult
Enrollment
24
Outcome Measure
Frontal lobe cerebral oxygenation, Determine the frontal lobe cerebral oxygantion by Near-Infrared Spectroscopy (NIRS),from before induction of spinal anaesthesia to end of surgery., Participants will be followed for the time in the operation theatre of the hospital stay, an expected average of 1 hour|Foetal heartrate, From before induction of spinal anaesthesia to 15 min after delivery, Participants will be followed for the time in the operation theatre of the hospital stay, an expected average of 1 hour
Sponsor Collaborator
Naestved Hospital|Rigshospitalet, Denmark
Funded By
OTHER
Location
Naestved Hospital, Naestved, 4700, Denmark
Other Id
2011-006103-35|SJ-271
Start Date
2012-02
Primary Completion Date
2012-07
Completion Date
2012-08
First Posted
2012-01-13
Results First Posted
Last Update Posted
2012-08-07
Study Document
Study Url
https://clinicaltrials.gov/study/NCT01509521
Title Cn
Title En
The Oxygenation of the Brain During Caesarean Section
Bilingual Status
semi_complete