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The effect of oral Aprepitant and Ondansetron injection on postoperative nausea and vomiting

Comparison of the effect of oral Aprepitant and Ondansetron injection individually and combining on postoperative nausea and vomiting after Laparoscopic cholecystectomy in women using general anesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016120831302N1
Enrollment
90
Registered
2017-05-17
Start date
2017-02-19
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

nausea and vomitting. Nausea and vomiting

Interventions

Intervention 1: group1: Ondancetron ampule 4mg intravenous after anesthetic induction and placebo capsule 1 hour before operation. Intervention 2: group 2: Aprepitant capsule 80mg 1 hour before operat
Treatment - Drugs
group1: Ondancetron ampule 4mg intravenous after anesthetic induction and placebo capsule 1 hour before operation
group 2: Aprepitant capsule 80mg 1 hour before operation and placebo ampule (normal saline) after anesthetic induction is administered
group 3: Aprepitant capsule 80mg 1 hour before operation and Ondansetron 4mg intravenous after anesthetic induction is administered

Sponsors

Vice President of Research, Kurdistan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: women between 18 to 50 years old with ASA class 1 and 2 with at least 2 criteria of APFEL (female; nonsmoker; motion sickness or PONV history; using opioids 100mcg fentanyl or equivalent ) Exclusion criteria: women under 18 or greater than 50 years old; AA class 3 or more; cholecystectomy in other anesthesia; systemic disease like diabetes; asthma; cardiovascular; reflux, severe obesity; pregnancy; breast feeding; hepatic and renal disease; neuromuscular disease; psychotic disease; addiction; acute cholecystitis.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Nausea and vomitting. Timepoint: 6 and 24 hours after operation. Method of measurement: VAS criteria.

Secondary

MeasureTime frame
Hospitalization period. Timepoint: at discharge time. Method of measurement: hospitalization days.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactReza Karami

Besat Hospital, Kurdistan University of Medical Sciences

reza_karami1367@yahoo.com+98 87 3322 8925

Outcome results

None listed

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