Status:
COMPLETED
The Effect of Magnesium Sulfate Infusion on the Quality of Recovery of Ambulatory Patients
Lead Sponsor:
Northwestern University
Conditions:
Pain
Opioid Use, Unspecified, Uncomplicated
Eligibility:
FEMALE
18-64 years
Phase:
NA
Brief Summary
A national survey has revealed that 80% of patients experienced pain after surgery and 86% of these patients had moderate, severe or extreme pain (1).Postoperative pain can extend recovery room stay a...
Eligibility Criteria
Inclusion
- undergoing lumpectomy
- ASA I and II
- Age between 18-64
Exclusion
- pregnancy
- breastfeeding -history of EKG abnormalities-
- kidney disease including: End Stage Renal Disease and polycystic kidney disease
- unable to understand the informed consent
- use of opioid in the last week
- use of calcium channel blockers
- Drop-out: surgeon or patient request
Key Trial Info
Start Date :
February 1 2011
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 1 2013
Estimated Enrollment :
50 Patients enrolled
Trial Details
Trial ID
NCT01433081
Start Date
February 1 2011
End Date
April 1 2013
Last Update
April 2 2014
Active Locations (1)
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1
Prentice Womens Hospital
Chicago, Illinois, United States, 60611