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A Closer Look at the Effect of Dextrose on Postoperative Nausea and Vomiting

A Closer Look at the Effect of Dextrose on Postoperative Nausea and Vomiting

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01123837
Enrollment
202
Registered
2010-05-14
Start date
2010-04-30
Completion date
2013-09-30
Last updated
2014-01-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative Nausea and Vomiting

Brief summary

The purpose of this investigator-initiated study is to see if giving dextrose fluid in the veins (IV) decreases the risk of postoperative nausea and vomiting (PONV) in female urologic, gynecologic and breast outpatient surgery patients and at what blood surgery level. The reason for this study is that IV dextrose has been shown to decrease the incidence of PONV and the use of medications to treat PONV, while leading to sooner discharge after surgery. This can decrease overall healthcare cost and improving patient satisfaction.

Interventions

The treatment group will receive a 250cc bolus over 2 hrs of D5LR prior to the end of surgery and continued in the PACU. Blood glucose will be checked 3 different times using an Accu-chek monitor along with the type and number of rescue medications given at 30, 60, and 120 minutes after anesthesia and the post-op morning. The control group will receive a 250cc bolus over 2 hours of LR. Blood glucose will be monitored 3 times along with the type and how much of rescue medications are given at 30, 60 and 120 minutes post-op and the morning after surgery.

OTHERD5LR or lactated ringers

The purpose of the study is to see if giving dextrose fluid in the veins (IV) decreases the risk of postoperative nausea and vomiting (PONV) in female urologic, gynecologic and breast outpatient surgery patients and at what blood sugar level. The reason for this study is that IV dextrose may decrease the incidence of PONV and the use of medications to treat PONV, while leading to sooner discharge after surgery. This can decrease overall healthcare cost and improving patient satisfaction.

Sponsors

Loma Linda University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 65 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
A Closer Look at the Effect of Glucose on Postoperative Nausea and Vomitingapproximately 24 hoursThe primary outcome measures will be the severity and incidence of PONV along with the type and number of rescue medications given at 0,30,60, and 120 minutes PACU time and the next morning.

Secondary

MeasureTime frameDescription
A Closer Look at the Effect of Dextrose on Post-operative nausea and vomitingapproximately 24 hoursSecondary endpoints recorded will be length of surgery, history of PONV, amount of pain medicine administered, blood loss, drop in BP \> 20%, unplanned hospital admission for PONV, and time till ready for discharge from PACU.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026