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UnknownNCT02082795

Investigating Women's Views on the Management of a Breech Pregnancy

Status
Unknown
Phase
Study type
Observational
Enrollment
15 (estimated)
Sponsor
Chelsea and Westminster NHS Foundation Trust · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

The investigators aim to perform a qualitative study to explore the views of women with a breech presentation on their management in general, and the use of anaesthesia or analgesia for ECV in particular.

Detailed description

Background Women undergo external cephalic version (ECV) in order to turn a baby in a breech (bottom, or feet down) presentation to a head down position. The procedure traditionally has about a 40% success rate and may be painful, issues that recent literature suggests puts some women off. Pain relief using a short acting morphine-like painkiller, called remifentanil, can significantly reduce the pain experienced but does not seem to improve ECV success rates. Alternatively, a spinal anaesthetic (similar to that used for a caesarean section) can be used. This increases success rates to around 60% and very effectively reduces pain; however, it is an invasive procedure with potential complications and requires a hospital stay of at least half a day. Aims and objectives The investigators aim to perform a qualitative study to explore the views of women with a breech presentation on their management in general, and the use of anaesthesia or analgesia for ECV in particular. Methods The investigators will use a semi-structured interview to explore the views of 10-15 expectant mothers recruited from the Breech Clinic at Chelsea and Westminster Hospital. Interviews will be recorded and then transcribed for thematic analysis by two researchers. Dissemination of output To our knowledge, this will be the first report on how women view the use of regional anaesthesia and remifentanil analgesia for ECV. In addition, we will add the views of our patient population to the existing literature concerning the management of ECV in general. The investigators anticipate that this information will be used to plan services and to guide future research.

Conditions

Timeline

Start date
2014-03-01
Primary completion
2014-08-01
Completion
2014-08-01
First posted
2014-03-10
Last updated
2014-03-10

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT02082795. Inclusion in this directory is not an endorsement.