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Clinical Trials/NCT01197950
NCT01197950
Completed
Not Applicable

A Randomized Controlled Trial of Acupuncture to Reduce Labour Pain

University of Skövde1 site in 1 country303 target enrollmentOctober 2008
ConditionsLabour Pain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Labour Pain
Sponsor
University of Skövde
Enrollment
303
Locations
1
Primary Endpoint
Use of Epidural Analgesia
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

The purpose of this study is to evaluate the effect of manual acupuncture and electro-acupuncture on labour pain.

Detailed Description

Acupuncture is used in obstetric care in spite of insufficient evidence of its potential to reduce labour pain. The findings so far are contradictory, which may reflect methodological limitations. The present study will take issues into account, such as sufficiently large sample to allow detection of possible differences between study groups; optimal timing of the intervention; controlling for intensity of the treatment; qualified training of persons giving the treatment; biological markers of pain and stress; possible effects on mother and infant; women's experiences such as overall birth experience and memory of pain.

Registry
clinicaltrials.gov
Start Date
October 2008
End Date
November 2011
Last Updated
3 years ago
Study Type
Interventional
Study Design
Factorial
Sex
Female

Investigators

Sponsor
University of Skövde
Responsible Party
Principal Investigator
Principal Investigator

Lena B Martensson

PhD RNM Senior Lecturer

University of Skövde

Eligibility Criteria

Inclusion Criteria

  • Admission to the labour ward in spontaneous onset of labour
  • Latent or active phase of labour
  • Nulliparity
  • Singleton pregnancy, cephalic presentation
  • Gestation: 37+0 to 41+6 (weeks + days)
  • Expressed need for labour pain relief
  • Swedish speaking (well enough to understand written and oral instructions)

Exclusion Criteria

  • No pharmacological pain relief within 24 hours prior to inclusion into the study
  • Severe preeclampsia
  • Treatment with oxytocin at the time point of allocation
  • Treatment with anticoagulant
  • Pacemaker

Outcomes

Primary Outcomes

Use of Epidural Analgesia

Time Frame: From start of treatment until birth

Frequecy of epidural analgesia

Study Sites (1)

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