Een verbetering van de analgesie na episiotomie door epidurale toediening van neostigmine en clonidine.
- Conditions
- Combinedn spinal-epidural analgesia during labour.
- Registration Number
- EUCTR2007-005512-12-BE
- Lead Sponsor
- niversity Hospitals Leuven
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Authorised-recruitment may be ongoing or finished
- Sex
- Female
- Target Recruitment
- Not specified
Inclusion Criteria
ASA I or II
nullipare
singleton pregnancy
> 37 weeks gestational stage
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 or IV
no episiotomy
allergy to local anesthetics
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Main Objective: Does the epidural administration of clonidine and neostigmine improves analgesia after episiotomy.;Secondary Objective: What is de incidence of advers events such as: nausea, vomiting, post dural punciton headache, pruritus, sedation, maternal hypotension and bradycardia.;Primary end point(s): Does the epidural administration of neostigmine and clonidine improves analgesia after episiotomy. Does the patient need less NSAID's and paracetamol after epidurale administration of neostigmine and clonidine.
- Secondary Outcome Measures
Name Time Method