Een gerandomiseerde studie naar epidurale analgesie bij aterme barende vrouwen.
Recruiting
- Registration Number
- NL-OMON25936
- Lead Sponsor
- Atrium Medical Centre Parkstad
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 200
Inclusion Criteria
Patients in order to be eligible for the trial, women have to:
1. Be 18 years or older;
Exclusion Criteria
Patient in order not to be eligible for the trial, women have to:
1. Be younger than 18 years;
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary outcome is maternal pain reduction during delivery, as measured on a VAS pain scale.<br><br>
- Secondary Outcome Measures
Name Time Method Secondary outcomes are the use of oxytocin, the number of instrumental vaginal deliveries, the number of caesarean sections, the duration of the second stage of labour, maternal hypotension, motor block, urine retention, fever, used antibiotics, used anaesthetics, neonatal condition (including Apgar scores and umbilical blood gasses), maternal experience and quality of life.<br>