John Radcliffe Hospital
Oxford, OX3 9DU, United Kingdom
NCT Number: NCT01165099
The study was primarily designed to assess the role of acupuncture in reducing the need for epidural analgesia for pain relief during induced labour. The other outcomes of labour were to be observed in addition.
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Notify Me18 year and older
Female
Interventional
Not applicable
Oxford, OX3 9DU, United Kingdom
The study was limited to women in their first pregnancy having labour induced for prolonged pregnancy or mild hypertension. The study involved randomised groups managed with manual acupuncture, electro acupuncture, sham acupuncture and a no-treatment control group.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The description of the acupuncture, whether manual, electro or sham, is as described for each of the individual groups.
Other names: Disposable needles Seirin DN04 0.20x30mm - 0.30x50mm., Electronic Acupunctuscope AWQ-104L digital.
Time frame: within 72 hours of trial entry
epidural analgesia administered during labour
Time frame: within 72 hours of trial entry
the outcomes of labour included: parenteral analgesia requirement, labour length, delivery mode, neonatal condition and postpartum haemorrhage
University of Oxford
Other
Acupuncture for Pain Relief During Induced Labour in Nulliparae: a Randomised Controlled Study
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