Using moxibustion to turn the breech baby
ISRCTN | ISRCTN98448646 |
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DOI | https://doi.org/10.1186/ISRCTN98448646 |
Secondary identifying numbers | N0234131719 |
- Submission date
- 30/09/2004
- Registration date
- 30/09/2004
- Last edited
- 28/10/2016
- Recruitment status
- No longer recruiting
- Overall study status
- Completed
- Condition category
- Pregnancy and Childbirth
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Record updated in last year
Plain English summary of protocol
Not provided at time of registration
Contact information
Mr T Draycott
Scientific
Scientific
Department of Obstetrics and Gynaecology
North Bristol NHS Trust
Southmead Hospital
Westbury-on-Trym
Bristol
BS10 5NB
United Kingdom
Phone | +44 (0)117 959 5176 |
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draycott_t@southmead.swest.nhs.uk |
Study information
Study design | Randomised controlled trial |
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Primary study design | Interventional |
Secondary study design | Randomised controlled trial |
Study setting(s) | Not specified |
Study type | Treatment |
Scientific title | Using moxibustion to turn the breech baby |
Study objectives | Does moxibustion to the classical acupuncture point bladder 67 increase the version rate to cephalic in uncomplicated breech pregnancies? |
Ethics approval(s) | Not provided at time of registration |
Health condition(s) or problem(s) studied | Breech pregnancy |
Intervention | A double blinded randomised controlled trial. Does moxibustion to the classical acupuncture point bladder 67 increase the version rate to cephalic in uncomplicated breech pregnancies? |
Intervention type | Other |
Primary outcome measure | Presentation of the baby one week after treatment and at delivery. |
Secondary outcome measures | Not provided at time of registration |
Overall study start date | 01/01/2004 |
Completion date | 01/07/2005 |
Eligibility
Participant type(s) | Patient |
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Age group | Adult |
Sex | Female |
Target number of participants | 210 |
Key inclusion criteria | 210 women aged 16-46 years with an uncomplicated breech pregnancy at 34-35 weeks. |
Key exclusion criteria | Not provided at time of registration |
Date of first enrolment | 01/01/2004 |
Date of final enrolment | 01/07/2005 |
Locations
Countries of recruitment
- England
- United Kingdom
Study participating centre
Department of Obstetrics and Gynaecology
Bristol
BS10 5NB
United Kingdom
BS10 5NB
United Kingdom
Sponsor information
Department of Health
Government
Government
Richmond House
79 Whitehall
London
SW1A 2NL
United Kingdom
Website | http://www.dh.gov.uk/Home/fs/en |
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Funders
Funder type
Government
North Bristol NHS Trust
No information available
Results and Publications
Intention to publish date | |
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Individual participant data (IPD) Intention to share | No |
IPD sharing plan summary | Not provided at time of registration |
Publication and dissemination plan | Not provided at time of registration |
IPD sharing plan |
Editorial Notes
28/10/2016: No publications found, verifying study status with principal investigator