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Clinical Trials/CTRI/2019/01/017309
CTRI/2019/01/017309
Completed
未知

A study to compare the anaesthetic properties of 0.5% Ropivacaine alone and in combination with Dexmedetomidine for ultrasound guided Supraclavicular brachial plexus block in patients undergoing upper limb surgery. - SCBPB

JLN MEDICAL COLLEGE AJMER0 sites100 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Health Condition 1: O- Medical and Surgical
Sponsor
JLN MEDICAL COLLEGE AJMER
Enrollment
100
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
June 15, 2018
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
JLN MEDICAL COLLEGE AJMER

Eligibility Criteria

Inclusion Criteria

  • Age group between 15 and 65 years.
  • Body weight 30 to 80 kg.
  • Patients belonging to ASA (American Society of Anaesthesiologists) class\-I and II.
  • Patients undergoing upper limb surgeries of duration 1\-2 hours in theatre with haemoglobin at least 9 gm/dl.
  • Patient free from any associated acute or chronic systemic illness.

Exclusion Criteria

  • Patients not willing to participate in the study.
  • Uncooperative patients.
  • Patient with chronic pain or on long\-term analgesics.
  • Any known hypersensitivity or contraindication to ropivacaine, dexmedetomidine.
  • Local pathology at the site of injection or disability limiting the performance of block.
  • Patients receiving beta blockers or cardiac drugs.
  • History of convulsion, allergy to the drug used, bleeding disorder, severe neurological deficit, thyroid disorder.
  • Patient with history of respiratory, cardiac, hepatic or renal disease (necessitating classification in ASA Class III or above).
  • Patients having a history of significant neurological, psychiatric, or neuromuscular disorders.
  • Pregnant, lactating mothers.

Outcomes

Primary Outcomes

Not specified

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