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N/A Completed N=200 Randomized Double-blind Prevention

Aprepitant for Post-operative Nausea

Postoperative Nausea
Source: ClinicalTrials.gov NCT01020903 ↗
Enrolled (actual)
200
Serious AEs
Results posted
Jun 2015
Primary outcomePrimary: Post-operative Nausea and Vomiting

Summary

Anesthesia, especially for laparoscopic surgery, can cause post-operative nausea and vomiting. Most patients are given two drugs, decadron and ondansetron, to try to minimize this. This study is to determine if a new drug, aprepitant, would add any benefit in terms of post-op nausea prevention. All laparoscopic cholecystectomy study patients will receive decadron and ondansetron. Half the patients will receive aprepitant in addition. The other half will receive placebo. The study will be randomized and double-blind.

Outcome Measures

OutcomeResultp-value
PRIMARY
Post-operative Nausea and Vomiting

Eligibility Criteria

Inclusion Criteria

  • Laparoscopic cholecystectomy patients.
  • Must be able to swallow a pill.

Exclusion Criteria

  • Liver failure,
  • Age less than 18.
  • Pregnancy, breast-feeding.
  • Pre-op vomiting.
  • Allergy to aprepitant.
  • Need for post-op gastric drainage.
  • Use of drugs that interact with aprepitant.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01020903). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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