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Effect of fasting time and Ondansetron on postoperative complications

Effect of reducing fasting time and Ondansetron on postoperative complications in orthopedic patients

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20171216037895N1
Enrollment
96
Registered
2018-09-24
Start date
2018-01-21
Completion date
Unknown
Last updated
2018-10-11

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

Conditions

Condition 1: Orthopedic diseases. Condition 2: Postoperative pain. Condition 3: Postoperative nausea and vomiting. Orthopedic aftercare Pain in limb, hand, foot, fingers and toes Nausea and vomiting

Interventions

Intervention 1: Intervention group 1: Two hours before surgery, 200 ml of 12.5% carbohydrates are given to the patient. This solution is prepared by the researcher. Each 100 ml contains 93.75 ml of de

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Desire and satisfaction to participate in the study People over 18 years old Patient should not be multiple trauma Elective and non-emergency surgery There is no history of allergy to ondanseton or other serotonin-receptor antagonists There is no problem or underlying illness associated with nausea and vomiting The patient does not have diabetes No report of severe nausea and vomiting within 24 hours or no use of anti-nausea and vomiting drugs 24 hours before surgery Not being a candidate for spinal anesthesia

Exclusion criteria

Exclusion criteria: People whose fasting time is less than 6 hours According to the doctor's opinion or anesthesiologist, it is necessary to prescribe preoperative Anti-nausea and vomiting drugs

Design outcomes

Primary

MeasureTime frame
Nausea. Timepoint: After the intervention, 6, 12 and 24 hours after full consciousness. Method of measurement: Questionnaire and observation.;Pain. Timepoint: After the intervention,Immediately 2, 4, 6, 12 and 24 hours after full consciousness. Method of measurement: Visual Analogue Scale.;Vomiting. Timepoint: After the intervention, 6, 12 and 24 hours after full consciousness. Method of measurement: Questionnaire and observation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohsen Torabi Khah

Esfahan University of Medical Sciences

m.torabikhah@nm.mui.ac.ir+98 31 3792 2918

Outcome results

None listed

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