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Clinical Trials/CTRI/2016/04/006880
CTRI/2016/04/006880
Completed
Phase 4

Comparative evaluation of volatile anesthetic agents for attenuation of venous cannulation pain: A prospective, randomized controlled study

Apollo Hospitals Bilaspur0 sites120 target enrollmentTBD

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Not specified
Sponsor
Apollo Hospitals Bilaspur
Enrollment
120
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

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

Investigators

Eligibility Criteria

Inclusion Criteria

  • ASA grade I and III

Exclusion Criteria

  • 1\.Patients with known sensitivity to study drugs
  • 2\.Subjects allergic to cotton or adhesive dressing, metal or plastic
  • 3\.History of acute or chronic pain or daily intake of analgesics
  • 4\.Calcium channel blocker or beta blocker within one month of recruiting
  • 5\.Abnormal skin conditions such as infection at the site of proposed venous cannulation
  • 6\.Cold hypersensitivity
  • 7\.Psychiatric patients

Outcomes

Primary Outcomes

Not specified

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