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NCT Number: NCT02115529

Study of Prevention of Postoperative Nausea and Vomiting Using Cesamet

Untreated, one third of patients undergoing general anesthesia will have postoperative nausea, vomiting, or both.

Patients often rate postoperative nausea and vomiting (PONV) as worse than postoperative pain. PONV increases the risk of aspiration and has been associated with suture dehiscence, esophageal rupture, subcutaneous emphysema, and bilateral pneumothoraxes. PONV frequently delays discharge, and is the leading cause of unexpected hospital admission after planned ambulatory surgery.

Nabilone (Cesamet®) is a synthetic cannabinoid developed in the 1970s which is a potent CB1 agonist. The use of nabilone in preventing nausea and vomiting in patients receiving chemotherapy has been thoroughly investigated. Results from clinical studies demonstrated the efficacy, safety, and tolerability of Cesamet in this population. There has been success in the past translating treatments for chemotherapy-induced nausea and vomiting (ie. 5-HT receptor agonists including Ondansetron and Granisetron) to use in the perioperative environment.

Only one RCT has studied the use of nabilone for the reduction of PONV. Published in 1995, this study compared the administration of either Cesamet 2 mg or metoclopramide 10 mg given 90 minutes before the operation in patients scheduled for elective hysterectomy in 60 women. This study failed to show any significant difference between groups. There are several limitations to this study including a poorly optimized dosing regimen, a small sample size, and a comparison group lacking clinical generalizability.

This study will investigate the use Cesamet vs Placebo, in addition to the regular antiemetic treatment which patients receive at the discretion of the managing anesthesiologist, for the prevention of PONV. The study group will include patients undergoing general anesthesia for elective ambulatory surgery with at least 3 risk factors (>60% risk) for the development of PONV.

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Key information

Age range

18 year–99 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

St Michael's Hospital

Toronto, Ontario, M5B 1W8, Canada

About this study

See above

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 18 or older with an American Society of Anesthesiologists (ASA) physical status of I to III who are scheduled to undergo elective surgery under general anesthesia with pre-anesthesia consultation prior to surgery.
  • Subjects must be able to swallow study medication;
  • At a risk of postoperative nausea and vomiting of at least 61% percent, according to a simplified risk score, based on the presence of at least three of the following risk factors: female sex, nonsmoker status, anticipated use of postoperative opioid and previous PONV or motion sickness.

Exclusion criteria

  • Subjects with clinically significant or unstable cardiac, respiratory, hepatic, renal, or other major organ system disease
  • Patients who will not be admitted to the PACU post-operatively (patients who are immediately transferred to the ICU)
  • Known sensitivity to marijuana or other cannabinoid agents
  • Psychotic illness or depression
  • Addiction to illicit substances or alcohol
  • Non-psychotic emotional disorders.
  • Pregnant or lactating
  • Subjects who suffer from chronic nausea and/or vomiting;
  • Has had treatment with any other investigational drug within 12 weeks prior to randomization
  • Subjects who, in the opinion of the investigator, would experience an unacceptable risk from administration of study drug

Treatment and study plan

Nabilone

Drug

Nabilone (0.5 mg) or placebo given preoperatively

Other names: Cesamet

Placebo

Drug

Placebo Comparator: identical capsule containing placebo (single dose) given preoperatively

Primary outcomes

  1. Incidence of postoperative nausea and/or vomiting

    Time frame: Prior to discharge from postanesthesia care unit, an expected average of two hours

Secondary outcomes

  1. Number of antiemetic rescue medications given postoperatively.

    Time frame: Prior to discharge from postanesthesia care unit, an expected average of two hours

Other outcomes

  1. Standardized score of nausea and/or vomiting severity if PONV occurs.

    Time frame: Prior to discharge from postanesthesia care unit, an expected average of two hours

  2. Pain score during the immediate post-operative period.

    Time frame: Prior to discharge from postanesthesia care unit, an expected average of two hours

  3. Use of intraoperative and postoperative opioids

    Time frame: Prior to discharge from postanesthesia care unit, an expected average of two hours

  4. Rates of known side effects.

    Time frame: Prior to discharge from postanesthesia care unit, an expected average of two hours

    Nabilone side effects include: drowsiness, vertigo, psychological high, dry mouth, depression, blurred vision, sensation disturbance, anorexia, headache, euphoria, and hallucinations (based on patient self-reporting).

  5. Time to discharge from the PACU.

    Time frame: Prior to discharge from postanesthesia care unit, an expected average of two hours

  6. Rates of admission due to PONV

    Time frame: Prior to discharge from postanesthesia care unit, an expected average of two hours

  7. Antiemetics given prophylactically by the anesthesiologist.

    Time frame: Until discharge from postanesthesia care unit, an expected average of two hours

Sponsors and collaborators

Lead sponsor

Unity Health Toronto

Other

Registry information

Official study title

A Randomized Controlled Trial of Cesamet(R) (Nabilone) for the Prevention of Postoperative Nausea and Vomiting in Elective Surgery

Acronym: Cesamet

Important dates

Study start
2014
Primary completion
2015
Study completion
2015
First posted
Apr 16, 2014
Registry last updated
Dec 3, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.