NCT01451762View on ClinicalTrials.gov

A Dose Ranging Effect of Preoperative Diphenhydramine on Postoperative Quality of Recovery After Ambulatory Surgery

NACompletedINTERVENTIONAL
Enrollment

90

Participants

Timeline

Start Date

September 30, 2011

Primary Completion Date

September 30, 2012

Study Completion Date

September 30, 2012

Conditions
SurgeryPain
Interventions
DRUG

.9 normal saline

.9 normal saline administered before surgery.

DRUG

25 mg diphenhydramine IV

25 mg diphenhydramine IV administered before surgery

DRUG

50 mg diphenhydramine IV

50 mg diphenhydramine administered IV before surgery

Trial Locations (2)

60611

Prentice Womens HOspital, Chicago

Prentice Womens HOsptial, Chicago

All Listed Sponsors
lead

Northwestern University

OTHER

NCT01451762 - A Dose Ranging Effect of Preoperative Diphenhydramine on Postoperative Quality of Recovery After Ambulatory Surgery | Biotech Hunter | Biotech Hunter