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Clinical Trials/CTRI/2017/05/008446
CTRI/2017/05/008446Completed未知

Comparative evaluation of duration of post operative analgesia and block characteristics with 0.5% ropivacaine versus 0.5% levobupivacaine in axillary brachial plexus blocks for isolated upper limb injuries, a double blinded prospective clinical study.

Dr ARathna0 sites70 target enrollmentStarted: TBDLast updated:

Trial Snapshot

Phase
未知
Status
Completed
Sponsor
Enrollment
70

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Inclusion Criteria

  • 1 Isolated forearm and hand injuries.
  • 2 Age group of 20 -65yrs belonging to ASA I and ASA II groups.

Exclusion Criteria

  • 1 Patients with known hypersensitivity to local anaesthetics, coagulopathy, infection at the site of block, peripheral neuropathy
  • 2 Patient refusal
  • 3 Age group below 20 and above 65 are excluded
  • Belonging to ASA III, IV
  • 4. Pregnant and lactating women

Investigators

Sponsor
Dr ARathna

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