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Clinical Trials/ACTRN12609000555257
ACTRN12609000555257
Completed
未知

A randomised controlled trial comparing pain scores for rectal Diclofenac with oral Diclofenac and oral or rectal Paracetamol in primiparous women after childbirth.

orthern Sydney & Central Coast Health, Human Research Ethics Committee0 sites240 target enrollmentJuly 8, 2009
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ConditionsPerineal painPain ManagementReproductive Health and Childbirth - Childbirth and postnatal care

Overview

Phase
未知
Intervention
Not specified
Conditions
Perineal pain
Sponsor
orthern Sydney & Central Coast Health, Human Research Ethics Committee
Enrollment
240
Status
Completed
Last Updated
6 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
July 8, 2009
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
Female

Investigators

Sponsor
orthern Sydney & Central Coast Health, Human Research Ethics Committee

Eligibility Criteria

Inclusion Criteria

  • •Primiparous women who have a second\-degree tear or greater or an episiotomy after a vaginal birth.

Exclusion Criteria

  • •Contraindications to non\-steroidal anti\-inflammatory medications
  • •History of gastrointestinal ulcer or bleeding
  • •Significant renal or liver impairment
  • •Preeclampsia and essential hypertension.
  • •Postpartum haemorrhage greater than 1000mL
  • •Medical disorders associated with a disturbed coagulation profile, in particular immune thrombocytopenic purpura, disseminated intravascular coagulation
  • •Women of non\-English speaking background
  • •Women taking anticoagulants, Lithium, Digoxin, Chloramphenicol or diuretics

Outcomes

Primary Outcomes

Not specified

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