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Résztvevőt keres itt: Egyesült Államok2. fázis

Rivastigmine for Antimuscarinic Delirium

A legfontosabb adatok

Ki végzi
Washington University School of Medicine
Hol
St Louis (Egyesült Államok)A helyszín megnézése
Azonosító
Állapot
Toboroz
Fázis
2. fázis
Résztvevők
42 fő, tervezett
Kezdés
2026. jún.
Várható befejezés
2028. dec.
A vizsgálat típusa
Beavatkozással járó, 2 csoportAz egyik csoport placebót (hatóanyag nélküli szert) kap, összehasonlításként.
A vizsgált kezelések
  • Rivastigmine
  • Placebo
A regiszteradat frissítve
2026. június 4.

Ki vehet részt

Életkor
10 év felett
Nem
Nők és férfiak
Egészséges önkéntesek
Nem vehetnek részt

A regiszter feltételei, szó szerint

Mind a 10 feltétel megnézéseKevesebb

Ki vehet részt

  • 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)

Ki nem vehet részt

  • 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

Helyszínek itt: Egyesült Államok

  • Washington University School of MedicineSt Louis, Egyesült ÁllamokContact: Kevin BaumgartnerRésztvevőt keres

A vizsgálatról

Mit akar kideríteni a vizsgálat

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.

A teljes eredeti leírásKevesebb

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.

A vizsgálat 2 csoportja

  • RivastigmineA vizsgált kezelés

    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, összehasonlításként

    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.

Kérdések a vizsgálat csapatának

  1. Milyen gyakran kell bejárnom, és egy-egy alkalom mennyi ideig tart?
  2. Megtérítik az utazási költséget?
  3. Megtarthatom a saját orvosomat?
  4. Mi történik, ha ki akarok lépni?

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

Oldal nyomtatása az orvosomnak

Adatok és források

Regiszteradat
Szerepel a ClinicalTrials.gov-on.
Hivatalos cím
Rivastigmine for Antimuscarinic Delirium: a Randomized, Placebo-controlled Trial
A regiszteradat frissítve
2026. június 4.