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Gastric UltrasoundNCT06567873

Gastric Ultrasound Assessment for Patients Taking Cannabis

An observational study of Gastric Ultrasound and Point of Care Ultrasound, run by Hospital for Special Surgery, New York at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The aim of this study is to perform bedside gastric point of care ultrasound (POCUS) exams to assess the gastric volume and content (clear liquids vs solid food) perioperatively in patients who report cannabis use. Read more about this study

Who is it for?
Ages 18 to 99 years
What is being tested?
Gastric Ultrasound Exam
How many people
40 participants
Where
1 siteUnited States
Study dates
9 May 2025to 14 Oct 2025
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 99 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: The study population will be comprised of patients scheduled for surgery at HSS who meet the following inclusion criteria and none of the exclusion criteria.

Who may be able to join

  • Any patient reporting preoperative cannabis usage within 1 month of surgery date

Who cannot join

  • Patient refusal to participate
  • Patient with gastric bypass or any other gastric surgery
  • Large hiatal hernia
  • Patients with large ascites
  • Patients on peritoneal dialysis
  • Emergency surgery
Show all 14Show fewer
  • Pre-existing diagnosis of gastroparesis
  • Parkinson's disease
  • Diabetes
  • Currently taking metformin
  • Chronic kidney disease stage 3 or higher
  • Creatinine ≥ 1.2
  • Esophageal surgery
  • Currently taking GLP1 agonist medication

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Hospital for Special Surgery

    New York, New York, 10021

Other trials in United States

About this study

Official title: Assessment of Preoperative Gastric Content With Ultrasound in Patients Reporting Cannabis Use

The aim of this study is to perform bedside gastric point of care ultrasound (POCUS) exams to assess the gastric volume and content (clear liquids vs solid food) perioperatively in patients who report cannabis use.

Read the detailed description

Cannabis use in the United States has continued to increase in recent years, particularly in the adult population. Ease of access through legalization paired with improved public perception has contributed to the uptick in cannabis use. The subset of cannabis users suffering from pain who present for surgery pose a risk for perioperative aspiration due to the slowing of gastric motility due to cannabis use. There is currently no adapted NPO guideline to account for cannabis use.

Gastric Ultrasound (GUS) can be used as a bedside tool for assessing a patient's stomach contents and risk of aspiration. GUS can identify whether a patient's stomach is empty or filled with clear liquid, thick liquid, or solid food. The volume of the stomach can be accurately calculated if there is clear liquid content. A full stomach is categorized as those with solid or thick liquid content or with clear liquid measuring more than 1.5 ml/kg body weight. As GUS is noninvasive and does not pose risk to patients, it is a useful tool assessing aspiration risk in the preoperative period.

Being tested
Gastric Ultrasound Exam
Keywords
cannabis, gastric ultrasound
Medical subject headings
Marijuana Abuse

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Gastric Ultrasound ExamOther

    A gastric ultrasound is a simple, fast, non-invasive bedside diagnostic test that provides a qualitative and quantitative assessment of gastric contents. There are no known risks of a gastric ultrasound exam.

Study groups in NCT06567873
Study groupRoleWhat they receive
Cannabis UsersThe cannabis user group will be comprised of patients who report preoperative cannabis use within 1 month of surgery date. This group will receive the ultrasound exam to assess stomach contents.
Receives: Other: Gastric Ultrasound Exam

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Incidence of delayed gastric emptying

    A full stomach on gastric ultrasound is defined by the presence of either solid food, thick liquids, or a specific volume (>1.5 ml/kg) of clear liquids on gastric ultrasound.

    Measured: This will be measured pre-operatively in the holding room area.

Secondary outcomes (3)
  1. Nothing by mouth (NPO) intervals

    Measure the NPO interval after last solid food and liquid consumption

    Measured: This will be measured pre-operatively in the holding room area.

  2. Presence of gastric peristalsis

    Gastric peristalsis will be graded as absent, slow, or normal on gastric ultrasound

    Measured: This will be measured pre-operatively in the holding room area.

  3. Time interval since last cannabis use

    Measure the time from last cannabis consumption to the time the gastric ultrasound was performed

    Measured: This will be measured pre-operatively in the holding room area.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted23 Aug 2024
  2. Study start9 May 2025
  3. Primary completion13 Oct 2025
  4. Study completion14 Oct 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Cross-sectional
Enrolment
40 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06567873
Sponsor's protocol ID
2024-1155
Status last verified
Nov 2025
First submitted
20 Aug 2024
Last updated
16 Dec 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • King DD, Stewart SA, Collins-Yoder A, Fleckner T, Price LL. Anesthesia for Patients Who Self-Report Cannabis (Marijuana) Use Before Esophagogastroduodenoscopy: A Retrospective Review. AANA J. 2021 Jun;89(3):205-212.

    PubMed 34042571
  • Cammarano CA, Villaluz JE. A Reason to Rethink Fasting Guidelines? Marijuana-Induced Gastroparesis and the Implications for Aspiration Risk in the Nil Per Os (NPO) Patient: A Case Report. Am J Case Rep. 2021 Nov 29;22:e934187. doi: 10.12659/AJCR.934187.

    PubMed 34840324
  • McCallum RW, Soykan I, Sridhar KR, Ricci DA, Lange RC, Plankey MW. Delta-9-tetrahydrocannabinol delays the gastric emptying of solid food in humans: a double-blind, randomized study. Aliment Pharmacol Ther. 1999 Jan;13(1):77-80. doi: 10.1046/j.1365-2036.1999.00441.x.

    PubMed 9892882
  • Esfandyari T, Camilleri M, Ferber I, Burton D, Baxter K, Zinsmeister AR. Effect of a cannabinoid agonist on gastrointestinal transit and postprandial satiation in healthy human subjects: a randomized, placebo-controlled study. Neurogastroenterol Motil. 2006 Sep;18(9):831-8. doi: 10.1111/j.1365-2982.2006.00834.x.

    PubMed 16918762

Questions about this trial

What is this clinical trial studying?

An observational study of Gastric Ultrasound and Point of Care Ultrasound, run by Hospital for Special Surgery, New York at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 14 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 16 Dec 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Incidence of delayed gastric emptying (time frame: This will be measured pre-operatively in the holding room area.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06567873, which also lists 4 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 Dec 2025.

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