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
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Moxibustion of the BL67 acupoint | Moxibustion 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.