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Effect of IV Dextrose on postoperative nausea and vomiting after laparoscopic cholecystectomy

Effect of IV dextrose 5% on incidence of postoperative nausea and vomiting after laparoscopic cholecystectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201504086803N9
Enrollment
132
Registered
2015-05-27
Start date
2014-05-31
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

postoperative nausea and vomiting after laparoscopic cholecystectomy. Vomiting following gastrointestinal surgery

Interventions

Intervention 1: infusion of 500cc solution containing 5% dextrose in Ringer Lactate whithin 30 minutes before induction of anesthesia. Intervention 2: infusion of 500cc solution containing Ringer La
Treatment - Drugs
Placebo
infusion of 500cc solution containing 5% dextrose in Ringer Lactate whithin 30 minutes before induction of anesthesia
infusion of 500cc solution containing Ringer Lactate whithin 30 minutes and before induction of anesthesia

Sponsors

Vice chancellor for research, Mazandaran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria included: (1) the desire to participate in the study, and informed consent(2) planned laparoscopic cholecystectomy surgery (3) age between 18-65 years. Exclusion criteria included: (1) At any time based on the patient's unwillingness to continue participating in study (2) Systemic hypertension (blood pressure above the 140/90 mm-Hg in two or more measurements(3) renal failure(4) coagulopathy (5)chronic heart failure, (6)liver failure(7) Diabetes mellitus (fasting morning glucose levels over 100 mg / dl)(8) previous history of severe nausea and vomiting after surgery (9)pregnancy(10) surgery prolonged more than 2 hours.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Incidence of nausea and vomiting. Timepoint: immediately and at 30, 60, 90, 120 after recovery and at 6, 12, 24 hours after being discharged from the recovery. Method of measurement: yes/no and Record in Questionnaire.

Secondary

MeasureTime frame
Intensity of nausea and vomiting. Timepoint: immediately and at 30, 60, 90, 120 after recovery and at 6, 12, 24 hours after being discharged from the recovery. Method of measurement: VRS(visual rating scale) and Record in Questionnaire.;Use of antiemetics. Timepoint: during 24 hours after surgery. Method of measurement: mg(miligram) and record in questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAbolfazl Firouzian MD

Mazandaran University of Medical Sciences

A.firouzian@mazums.ac.ir; Ab.firouzian@gmail.com+98 11 3337 5038

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026