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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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19 February 2015 |
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Main ID: |
NCT00890474 |
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Date of registration:
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28/04/2009 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Moxibustion for Fetus in Breech Presentation
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Scientific title:
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Moxibustion for Fetus in Breech Presentation |
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Date of first enrolment:
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October 2004 |
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Target sample size:
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212 |
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Recruitment status: |
Completed |
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URL:
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http://clinicaltrials.gov/show/NCT00890474 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Caregiver), Primary Purpose: Treatment
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Phase:
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Phase 3
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Countries of recruitment
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Switzerland
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Breech presentation
- 34 to 36 weeks of gestation
- Single fetus
Exclusion Criteria:
- Uterine malformation
- Placenta praevia
- Transverse lie
Age minimum:
N/A
Age maximum:
N/A
Gender:
Female
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Health Condition(s) or Problem(s) studied
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Breech Presentation
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Intervention(s)
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Procedure: Moxibustion of the BL67 acupoint
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Primary Outcome(s)
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Cephalic presentation at delivery or before external cephalic version
[Time Frame: end of pregnancy]
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Secondary Outcome(s)
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Women's views on the intervention
[Time Frame: end of pregnancy]
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Mode of delivery
[Time Frame: end of pregnancy]
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External cephalic version
[Time Frame: end of pregnancy]
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Secondary ID(s)
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Moxibustion_siege
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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