ITCMDBv1
Clinical TrialID 5587

Phenylephrine in Spinal Anesthesia in Preeclamptic Patients

NCT00458003

Preeclampsia|Hypotension

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Trial: 1Ingredient: 1Links: 1
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Record Fields

Scalar fields from the final clinical_trial record.

Clinical Trial Id
5587
Evidence Id
5587
Core Evidence Id
5587
Source Clinical Trial Id
5572
Herb2 Clinical Trial Id
HBCT005572
Nct Id
NCT00458003
Title
Phenylephrine in Spinal Anesthesia in Preeclamptic Patients
Status
Completed
Phase
Study Result
Yes
Study Condition
Preeclampsia|Hypotension
Study Type
Interventional
Study Design
Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: DOUBLE (PARTICIPANT, INVESTIGATOR)|Primary Purpose: TREATMENT
Intervention
DRUG: Ephedrine|DRUG: Phenylephrine
Intervention Allocation
Randomized
Intervention Model
Parallel
Intervention Mask
Double
Intervention Purpose
Treatment
Gender
Female
Age
Adult
Enrollment
110
Outcome Measure
The Umbilical Artery pH, The umbilical artery blood pH immediately after delivery. The pH scale ranges from 0 to 14. A normal pH sample from the umbilical artery ranges from pH: 7.18 - 7.38. The lower the pH the more acidic and the higher the pH the more basic., Immediately after delivery
Sponsor Collaborator
Northwestern University
Funded By
OTHER
Location
Northwestern Memorial Hospital, Chicago, Illinois, 60611, United States|Northwestern University, Chicago, Illinois, 60611, United States
Other Id
0524-31
Start Date
2006-07
Primary Completion Date
2016-12
Completion Date
2016-12
First Posted
2007-04-09
Results First Posted
2022-06-02
Last Update Posted
2022-06-02
Study Document
Study Url
https://clinicaltrials.gov/study/NCT00458003
Title Cn
Title En
Phenylephrine in Spinal Anesthesia in Preeclamptic Patients
Bilingual Status
semi_complete