Status:

COMPLETED

Oral Paracetamol as Preemptive Analgesia for Labor Pain

Lead Sponsor:

Ain Shams University

Conditions:

Labor Pain

Eligibility:

FEMALE

18-40 years

Phase:

PHASE3

Brief Summary

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

Detailed Description

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

Eligibility Criteria

Inclusion

  • primigravida
  • The gestational age between 37- 42 weeks
  • Not seeking analgesia
  • Singleton pregnancy
  • vertex
  • Spontaneous onset of labour
  • 1st stage of labour (less than 5 cm)

Exclusion

  • Extreme of age (below18-above 40)
  • Multiparous
  • Multiple gestation
  • Malpresentation
  • Congenital or acquired pelvic abnormalities(eg. Poliomyelitis)
  • Any medical disorder with pregnancy
  • Induction of labour
  • Advanced 1st stage \> 5 cm
  • Use of any other kind of analgesia before recruitment in the study
  • Scared uterus
  • Fetal distress

Key Trial Info

Start Date :

December 1 2011

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

June 1 2012

Estimated Enrollment :

100 Patients enrolled

Trial Details

Trial ID

NCT01817829

Start Date

December 1 2011

End Date

June 1 2012

Last Update

March 26 2013

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