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Taking people in United StatesPhase 2

Rivastigmine for Antimuscarinic Delirium

Key facts

Who runs it
Washington University School of Medicine
Where
St Louis, United StatesSee the site
Trial code
Status
Recruiting
Phase
Phase 2
People taking part
42 people, planned
Started
Jun 2026
Expected to end
Dec 2028
Type of study
Interventional, 2 groupsOne group gets a placebo (a dummy treatment), for comparison.
Treatments tested
  • Rivastigmine
  • Placebo
Record updated
4 June 2026

Who can take part

Age
10 years and older
Sex
Women and men
Healthy volunteers
Cannot take part

The registry criteria, word for word

Show all 10 criteriaShow less

Who can take part

  • 10 years of age or older
  • Diagnosis of antimuscarinic delirium by history and physical examination, in the opinion of the treating attending toxicologist
  • Reasonably likely to benefit from antidotal therapy for antimuscarinic delirium, as demonstrated by clinically significant agitation and delirium:; Richmond Agitation-Sedation Scale (RASS) of +1 or higher at the time of enrollment; Positive for delirium as defined by the Confusion Assessment Method for the ICU (CAM-ICU)

Who cannot take part

  • Inability to safely tolerate oral medication, in the judgement of the treating attending physician
  • Any known allergy or intolerance to rivastigmine or other AChEI
  • Evidence of significant risk for serious cardiac or neurologic sequelae of antimuscarinic poisoning:; Any known or suspected seizure activity prior to enrollment b. QRS duration >100 milliseconds on EKG at enrollment c. Any ventricular dysrhythmia prior to enrollment d. Respiratory failure of any etiology requiring endotracheal intubation e. Any hypotension at enrollment: i. Adults: systolic blood pressure (SBP) <90 mmHg ii. Children ≥10: systolic blood pressure (SBP) <90 mmHg, as per Pediatric Advanced Life Support (PALS) age-based cutoff for children 10 years of age or older3 f. Any administration of sodium bicarbonate, hypertonic saline, vasopressors, inotropes, antiarrhythmic agents, or intravenous lipid emulsion prior to enrollment; Unacceptable risk of serious medical sequelae of antimuscarinic poisoning in the judgment of the treating attending toxicologist
  • Age less than 10 years at time of enrollment
  • Evidence of significant risk of adverse effect of AChE-I:; a.Bradycardia or risk of AChE-I induced bradycardia at enrollment: i. Adults: heart rate (HR) <80 beats per minute ii. Children: heart rate below the median heart rate for age as proposed by Fleming et al.33:; Ages 10-12: HR <84 beats per minute 2. Ages 12-15: HR <78 beats per minute 3. Ages 15-18: HR <73 beats per minute b. Known or suspected seizure disorder. c. History of asthma or COPD or wheezing during index presentation d. Known or suspected physical obstruction of intestinal or urogenital tract i. Ileus and/or urinary retention due to antimuscarinic poisoning do not exclude patients from enrollment; Known or suspected peptic ulcer disease
  • Surrogate decision maker not available to provide informed consent for enrollment
  • Patient is pregnant or a ward of the state

Where in United States

  • Washington University School of MedicineSt Louis, United StatesContact: Kevin BaumgartnerTaking people

About the trial

What the trial wants to find out

Antimuscarinic delirium (AMD) is a common and dangerous toxicology condition caused by poisoning by medications and other chemicals that block muscarinic receptors. Physostigmine, the standard antidote for AMD, currently has very limited availability in the United States due to an interruption of production.

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Recent case reports and small observational studies suggest that rivastigmine might be useful in the treatment of AMD, but there is not direct prospective evidence comparing rivastigmine to physostigmine or supportive care. In order to investigate the effectiveness of rivastigmine, the investigators propose a randomized, placebo-controlled clinical trial of rivastigmine for AMD. The investigators hypothesize that patients treated with rivastigmine for antimuscarinic delirium will experience more rapid resolution of agitation and delirium than those treated with placebo.

The 2 groups in the trial

  • RivastigmineTreatment being tested

    Patients in the rivastigmine arm will receive rivastigmine 3mg by mouth once, followed by rivastigmine 1.5mg by mouth every 1 hour as needed for ongoing delirium or agitation (at the discretion of the treating physician), for up to three doses.

  • PlaceboPlacebo, for comparison

    Patients in the placebo arm will receive oral placebo by mouth once, followed by oral placebo every 1 hour as needed for ongoing delirium or agitation (at the discretion of the treating physician), for up to three doses.

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Official title
Rivastigmine for Antimuscarinic Delirium: a Randomized, Placebo-controlled Trial
Record updated
4 June 2026