Clinical Trials Directory

Trials / Completed

CompletedNCT00245752

Can Acupuncture be Used as Preparation for Induction of Labour

Randomised Study of the Effect of Acupuncture as Induction of Labour

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
125 (actual)
Sponsor
Aarhus University Hospital Skejby · Academic / Other
Sex
Female
Age
Healthy volunteers
Accepted

Summary

The purpose of the study is to evaluate whether acupuncture can be used to ripen cervix before medicinal induction of labor or even be used as method for induction, and thereby eliminating other and more potentially harmful methods.

Detailed description

Acupuncture has become a natural part of the range of treatments in obstetric departments in Denmark, but there is only little evidence to the effect of acupuncture. Many of the induction procedures currently in use in Denmark also have a little risk of side effects. to mention a few: There is a increased risk of maternal and neonatal infection, bleeding, ruptured membranes and placental disruption as result of the use of endocervical balloon catheter. In connection with manual rupture of membranes there is an increased risk of umbilical prolapse, maternal and neonatal infection, affected fetal heart rate, scratches on the scalp and placental bleeding. By using misoprostol there has been seen hyperstimulation of uterus causing affected fetal heart rate. Many women are asking for alternatives to the existing methods used in obstetric dept.s. In order to assess the effect, or lack of, acupuncture might have, we want to use acupuncture in the study group on acupuncture points on hands, feet, ankles and back of the head. The control group will get placebo acupuncture needles on same locations. The included women will be treated with the kind of acupuncture that counts for the group to which shes been allocated on gestational age 41+6 at 8:00 am and 2:30 pm.

Conditions

Interventions

TypeNameDescription
DEVICEacupunctureacupuncture in points bilaterally: BL 67, LI 4, SP6, one in GV20.

Timeline

Start date
2005-11-01
Primary completion
2008-07-01
Completion
2008-12-01
First posted
2005-10-28
Last updated
2009-02-05

Source: ClinicalTrials.gov record NCT00245752. Inclusion in this directory is not an endorsement.