Clinical Trials Directory

Trials / Completed

CompletedNCT00890474

Moxibustion for Fetus in Breech Presentation

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
212 (actual)
Sponsor
University Hospital, Geneva · Academic / Other
Sex
Female
Age
Healthy volunteers
Not accepted

Summary

Objective: To evaluate moxibustion of the BL67 acupoint between 34 and 38 weeks of gestation to facilitate cephalic version of breech presentation in a Western setting. The hypothesis is that moxibustion increase the likelihood of cephalic version. Design: Randomised controlled trial Setting: University hospital. Population: A total of 212 consenting women between 34 and 36 weeks of gestation with a single fetus in breech presentation will be randomised to moxibustion (n=106) or expectant management (n=106). Main Outcome Measure: Cephalic presentation at delivery or before external cephalic version.

Conditions

Interventions

TypeNameDescription
PROCEDUREMoxibustion of the BL67 acupointMoxibustion sessions every day (every other day in hospital, self-administration at home the other day) during a maximum of 14 days. Stopped if cephalic version.

Timeline

Start date
2004-10-01
Primary completion
2008-12-01
Completion
2009-01-01
First posted
2009-04-29
Last updated
2009-04-29

Locations

1 site across 1 country: Switzerland

Source: ClinicalTrials.gov record NCT00890474. Inclusion in this directory is not an endorsement.