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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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19 February 2015 |
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Main ID: |
NCT01394731 |
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Date of registration:
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12/07/2011 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Analgesic Effects of Intravenous Paracetamol on Labor Pain
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Scientific title:
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Analgesic Effects of Intravenous Acetaminophen on Labor Pain |
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Date of first enrolment:
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December 2010 |
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Target sample size:
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Recruitment status: |
Completed |
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URL:
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http://clinicaltrials.gov/show/NCT01394731 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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Phase:
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Phase 4
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Countries of recruitment
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Saudi Arabia
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- American Society of Anesthesiologists physical class I-II
- term patients (= 37 weeks of gestation)
Exclusion Criteria:
- previous cesarean section
- hypertension, pre-eclampsia, eclampsia
- intra-uterine growth retardation
- intrauterine fetal death
- morbid obesity (body mass index = 35)
- allergy to any of the study drugs
Age minimum:
18 Years
Age maximum:
60 Years
Gender:
Female
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Health Condition(s) or Problem(s) studied
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Labor Pain
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Intervention(s)
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Drug: Acetaminophen
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Drug: Meperidine
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Primary Outcome(s)
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Visual analogue scale (VAS) score for pain
[Time Frame: Up to 24 hours]
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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