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Birth canal dilator study

Not Applicable
Conditions
Pregnancy and Childbirth
labour, delivery
Registration Number
PACTR201801002864315
Lead Sponsor
Effective Care Research Unit, University of Witwatersrand and Fort Hare
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Female
Target Recruitment
0
Inclusion Criteria

Nulliparous women
Aged 18 years or above
No major complications of pregnancy
In active labour
Vaginal birth anticipated
Consent given

Exclusion Criteria

Any contra-indication to use of dilator

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Spontaneous delivery within 15 minutes of bearing down
Secondary Outcome Measures
NameTimeMethod
Assisted delivery;Caesarean section;Episiotomy;Perineal tears;Number of perineal sutures;Apgar score;Arterial cord blood pH or lactate;Maternal satisfaction;Urinary incontinence;Flatus incontinence;Faeces incontinence;Perineal pain;Dyspareunia
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