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Epidural pain relief and the outcome of labour

Not Applicable
Recruiting
Conditions
Pelvic floor trauma following vaginal delivery
Reproductive Health and Childbirth - Other reproductive health and childbirth disorders
Renal and Urogenital - Other renal and urogenital disorders
Anaesthesiology - Pain management
Registration Number
ACTRN12614000448640
Lead Sponsor
Prof. Hans Peter Dietz
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
200
Inclusion Criteria

1.Primigravidas or those without previous pregnancies that progressed to 20+ weeks of gestation.
2.Singleton pregnancy.
3.Aiming for vaginal delivery.
4.Participant is able to understand the risks and potential benefits of participating in the study.
5.Participant is willing and fit to provide a written consent.
6.Participant is willing and has the ability to comply with specified follow-up evaluations.
7.Aged 16 and above

Exclusion Criteria

1.Contraindication to epidural.
2.Neurological disease.
3.Muscular or skin disorder affecting tissue elasticity.
4.Previous pelvic surgery affecting vaginal anatomy.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pelvic floor trauma namely perineal tears, vaginal tears, anal sphincter injuries and levator ani avulsions, assessed by clinical examination and translabial and transperineal ultrasound.[3 months and 2 years postpartum.]
Secondary Outcome Measures
NameTimeMethod
The obstetric outcomes as a composite outcome : the length of first and second stage of labour, rate of instrumental delivery and caesarean section, obtained from review electronic medical and labour records.[Immediate postpartum];The clinical efficacy (analgesia, motor and sympathetic block); assessed by the Bromage score.[In labour (intrapartum)]
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