Labor Analgesia With Ropivacaine and Clonidine
- Registration Number
- NCT00626977
- Lead Sponsor
- UPECLIN HC FM Botucatu Unesp
- Brief Summary
The aim of the present study was to examine, for pain relief during labor, the efficacy of two pharmacological approaches - the 0.125% ropivacaine alone and the 0.0625% ropivacaine added to 75 ug clonidine, both by epidural administration. The effect of the drugs on mother and newborn was also determined.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 32
Inclusion Criteria
- Singleton healthy
- Full-term pregnancy
- American Society of Anesthesiologists physical status I or II
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Exclusion Criteria
- Patients who had received opioids
- History of hypersensitivity to local anesthetic or to clonidine
- Fetus showed signs of possible intrauterine suffering
- Fetus showed signs of possible neurological deficit
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Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description R ropivacaine R group:15 mL of 0.125% ropivacaine (18.75 mg) RC ropivacaine and clonidine RC group:0.0625% ropivacaine (9.375 mg) plus 75 ug clonidine
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
College of Medicine of Botucatu
🇧🇷Botucatu, São Paulo, Brazil