Status:
COMPLETED
A Dose Ranging Effect of Preoperative Diphenhydramine on Postoperative Quality of Recovery After Ambulatory Surgery
Lead Sponsor:
Northwestern University
Conditions:
Surgery
Pain
Eligibility:
FEMALE
18-64 years
Phase:
NA
Brief Summary
Pain after ambulatory surgery remains an unsolved problem in The United States and Europe. It is associated with delayed hospital discharge and it can result to an increased opioid consumption with ad...
Eligibility Criteria
Inclusion
- Age 18-64 years
- Patients undergoing ambulatory surgery
- ASA PS I, II.
Exclusion
- Chronic opioid use
- pregnant patient or lactating patients
- allergy to diphenhydramine
- glaucoma
- uncontrolled hypertension
- asthma
- hyperthyroidism
- cardiovascular disease
Key Trial Info
Start Date :
September 1 2011
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
September 1 2012
Estimated Enrollment :
90 Patients enrolled
Trial Details
Trial ID
NCT01451762
Start Date
September 1 2011
End Date
September 1 2012
Last Update
March 14 2014
Active Locations (2)
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1
Prentice Womens HOspital
Chicago, Illinois, United States, 60611
2
Prentice Womens HOsptial
Chicago, Illinois, United States, 60611