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Oral Paracetamol as Preemptive Analgesia for Labor Pain

NCT01817829 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2013-03-26

No results posted yet for this study

Summary

It is a double blinded randomized control trial assessing the use of Oral paracetamol in managing the intrapartum pain.

Conditions

  • Labor Pain

Interventions

DRUG

paracetamol

500 mg oral tablet

DRUG

placebo

Sponsors & Collaborators

  • Ain Shams University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
40 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-12-31
Primary Completion
2012-06-30
Completion
2012-06-30

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01817829 on ClinicalTrials.gov