Onderhoud van de analgesie tijdens de arbeid na gecombineerde spinale epidurale anesthesie: ”positieve invloed op kwaliteit van analgesie door patient-controlled epidural analgesia met clonidine en neostigmine?”
- Conditions
- Combined spinal -epidural analgesia during labour.
- Registration Number
- EUCTR2009-014362-25-BE
- Lead Sponsor
- Marc Van de Velde
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Authorised-recruitment may be ongoing or finished
- Sex
- Female
- Target Recruitment
- 100
Inclusion Criteria
ASA I or II
Singleton pregnancy, vertex presented
> 37 weeks post-conception
Nomal pregnancy
Informed written consent
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range
Exclusion Criteria
ASA III and IV
Maternal length < 150 cm and BMI > 40
Suspected congenital disorder
Multiple pregnancy
VAS < 50 mm
Allergic to local anesthetics
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method