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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 14 January 2013
Main ID:  NCT01123837
Date of registration: 12/05/2010
Primary sponsor: Loma Linda University
Public title: A Closer Look at the Effect of Dextrose on Postoperative Nausea and Vomiting
Scientific title: A Closer Look at the Effect of Dextrose on Postoperative Nausea and Vomiting
Date of first enrolment: April 2010
Target sample size: 100
Recruitment status: Active, not recruiting
URL:  http://clinicaltrials.gov/show/NCT01123837
Study type:  Interventional
Study design:  Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Prevention  
Countries of recruitment
United States
Contacts
Name:   Parul Patel, M.D.
Address: 
Telephone:
Email:
Affiliation:  Loma Linda University Medical Center
Key inclusion & exclusion criteria

Inclusion Criteria:

1. ASA I or II

2. female urologic, gynecologic and breast surgery patients undergoing scheduled same
day procedures at LLUMC Heart and Surgical Hospital

Exclusion Criteria:

1. age <18 or >65;

2. severe hypertension,diabetes mellitus, significant hepatic or renal disease

3. excessive blood loss

4. sustained (>10 min)>20% from baseline drop in BP after treatment

5. inability to follow protocol

6. refusal to sign consent



Age minimum: 18 Years
Age maximum: 65 Years
Gender: Female
Health Condition(s) or Problem(s) studied
Postop Nausea and Vomiting
Intervention(s)
Other: D5LR or lactated ringers
Other: Intravenous fluid
Primary Outcome(s)
A Closer Look at the Effect of Glucose on Postoperative Nausea and Vomiting [Time Frame: approximately 24 hours]
Secondary Outcome(s)
A Closer Look at the Effect of Dextrose on Post-operative nausea and vomiting [Time Frame: approximately 24 hours]
Secondary ID(s)
5100086
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
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