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Clinical Trials/CTRI/2019/01/017195
CTRI/2019/01/017195
Not yet recruiting
未知

A prospective randomized double blinded controlled study to evaluate the efficacy of perioperative intravenous magnesium with lignocaine in post operative opioid requirement in patients undergoing elective spine surgeries

MIOT Hospital0 sites0 target enrollmentTBD
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ConditionsHealth Condition 1: O- Medical and Surgical

Overview

Phase
未知
Intervention
Not specified
Conditions
Health Condition 1: O- Medical and Surgical
Sponsor
MIOT Hospital
Status
Not yet recruiting
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
MIOT Hospital

Eligibility Criteria

Inclusion Criteria

  • •1\.American society of anesthesiologists physical status class I and II
  • •2\.Age between 18 to 60 years

Exclusion Criteria

  • •1\.Patients undergoing emergency surgery
  • •2\.Patients with pre\-existing neurological disorders
  • •3\.Patients with liver and renal disease
  • •4\.Patients with psychiatric illness
  • •5\.Patients on antiepileptic medication
  • •6\.Patients with history of allergy to magnesium or lignocaine
  • •7\.Patients with cardiac conduction abnormality
  • •8\.Patients on chronic opioid therapy
  • •9\.Patients on calcium channel blockers
  • •10\.Patients with ASA III, IV and V status

Outcomes

Primary Outcomes

Not specified

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