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Labor Analgesia With Ropivacaine and Clonidine

Completed
Conditions
Labor Pain
Interventions
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
GroupInterventionDescription
RropivacaineR group:15 mL of 0.125% ropivacaine (18.75 mg)
RCropivacaine and clonidineRC group:0.0625% ropivacaine (9.375 mg) plus 75 ug clonidine
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

College of Medicine of Botucatu

🇧🇷

Botucatu, São Paulo, Brazil

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