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Clinical Trials/CTRI/2017/01/007715
CTRI/2017/01/007715
Completed
未知

Comparison of continuous epidural infusion of 0.125 percent Ropivacaine with 1 micro gram per millilitre of Fentanyl versus 0.125 percent Bupivacaine with 1 micro gram per millilitre of Fentanyl for postoperative analgesia for major abdominal surgeries

il0 sites60 target enrollmentTBD
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ConditionsHealth Condition 1: null- Major abdominal surgeries

Overview

Phase
未知
Intervention
Not specified
Conditions
Health Condition 1: null- Major abdominal surgeries
Sponsor
il
Enrollment
60
Status
Completed
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
il

Eligibility Criteria

Inclusion Criteria

  • •American Society of Anaesthesiology class I and II patients for major abdominal surgeries
  • •Age 18 to 65 years

Exclusion Criteria

  • •American Society of Anaesthesiology class III and IV
  • •Infection at Injection site
  • •Patient refusal
  • •Coagulopathy or bleeding disorder
  • •Severe Hypovolemia
  • •Increased intracranial pressure
  • •Pre existing neurological deficit and demyelinating lesion
  • •Severe spinal deformities

Outcomes

Primary Outcomes

Not specified

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