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The effect of dextrose injection in preventing postoperative nausea and vomiting in patients undergoing cholecystectomylaparoscopic surgery

The effect of dextrose injection in preventing postoperative nausea and vomiting in patients undergoing cholecystectomylaparoscopic surgery

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20141209020258N176
Enrollment
100
Registered
2022-10-03
Start date
2022-10-07
Completion date
Unknown
Last updated
2022-11-21

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

Conditions

Cholecystectomy laparoscopic surgery. Retained cholelithiasis following cholecystectomy

Interventions

Intervention 1: Intervention group: 10 millileter in kilogeram in hour of Ringer's lactate serum along with 500 miligram in kilogeram of 5% dextrose will be given. The solutions are infused 5 minutes

Sponsors

Arak University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 70 Years

Inclusion criteria

Inclusion criteria: All candidates for laparoscopic cholecystectomy Age between 30 and 70 years ASA class I and II Patients under general anesthesia The duration of surgery is between 60-150 minutes Absence of Parkinson's disease, motion sickness or history of chemotherapy Absence of diabetes

Exclusion criteria

Exclusion criteria: All patients who do not undergo general anesthesia for any reason. Patients who suffer cardiac arrest during surgery. Patients whose surgery lasts more than 180 minutes. Patients who are referred to the intensive care unit for any reason.

Design outcomes

Primary

MeasureTime frame
Vomitting. Timepoint: In recovery, 2, 4, 6, 12 and 24 hours after the operation. Method of measurement: Score from 0 to 4 (no vomiting gets zero and frequent vomiting gets 4.).;Severe nausea. Timepoint: Recovery, 2, 4, 6, 12 and 24 hours after the operation. Method of measurement: VAS visual analog scale.;Mean of dose of metoclopramide in 24 hours. Timepoint: At the end of the study. Method of measurement: Physical examination.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Hesamedin Modir

Arak University of Medical Sciences

modir.he@gmail.com+98 86 3222 2003

Outcome results

None listed

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