Status:
COMPLETED
Determination of the Minimum Local Analgesic Dose of Spinal Chloroprocaine in Labour
Lead Sponsor:
University Hospital, Ghent
Conditions:
Pain Relief During Labour
Eligibility:
FEMALE
20-45 years
Phase:
PHASE4
Brief Summary
Combined spinal-epidural (CSE) analgesia has become a widely accepted approach to provide analgesia for labour pain. Despite the increasingly widespread use of this technique, an optimal intrathecal d...
Eligibility Criteria
Inclusion
- Inclusion criteria :
- Pregnant women in labour with a gestational period of 36 to 41 weeks
- ASA I or II
- Primi- and multiparae
- Spontaneous or induced labor
- Exclusion criteria :
- Pregnant women in labour who received opiates or analgetics during the 6 hour period prior to CSE
Exclusion
Key Trial Info
Start Date :
October 17 2013
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 18 2017
Estimated Enrollment :
40 Patients enrolled
Trial Details
Trial ID
NCT01909089
Start Date
October 17 2013
End Date
October 18 2017
Last Update
December 9 2022
Active Locations (1)
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1
Ghent University Hospital
Ghent, Belgium, 9000