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Condition

Delirium Clinical Trials

Studies of delirium, matched by condition name and medical subject headings. Start with those open to enrolment.

1,711 registered studies

In numbers

Open to volunteers
365
Active
415
With results posted
124
All registered
1,711

Open to volunteers: recruiting, not yet recruiting or enrolling by invitation. Active adds studies under way that have stopped recruiting.

Open to volunteers

All 365
  • Delirium, Intensive Care Unit Delirium

    Family-partnered Delirium Prevention, Detection, and Management in the ICU

    • Not yet recruiting
    • Age: 18 years and older
    • Lifestyle or therapy programme

    Almost half of critically ill patients experience delirium. Delirium is associated with impaired cognition, mortality, and increased healthcare costs.

    Conditions
    Delirium, Intensive Care Unit Delirium, Post Intensive Care Unit Syndrome, Post Intensive Care Unit Syndrome Family
    Trial name
    ACTIVATE (NCT07896356)
    Testing
    Standard of Care, Delirium Education, Prevention, and Management
    Where
    Canada
    Volunteers
    1,344 people
    Sponsor
    University of Calgary
    Can I take part? ACTIVATE
  • Lactium, Premedication

    Lactium Premedication to Prevent Emergence Agitation

    • Not yet recruiting
    • Age: 3 to 12 years
    • Phase 3

    This biased coin sequential allocation, dose finding study will be conducted to determine the effective dose of oral lactium in 90% of children (ED90) for prevention of emergence agitation during recovery from adenotonsillectomy.

    Conditions
    Lactium, Premedication, Emergence Agitation, Adenotonsillectomy
    Trial name
    NCT07894484
    Testing
    Lactium
    Where
    Egypt
    Volunteers
    40 people
    Sponsor
    Tanta University
    Can I take part? NCT07894484
  • Neurocognitive Disorders, Postoperative Delirium

    Creatine and Perioperative Brain Health

    • Not yet recruiting
    • Age: 60 to 85 years

    The overall goal of this study is to explore the effects of perioperative oral creatine supplementation on cognitive function and physiological responses to surgery in older adults.

    Conditions
    Neurocognitive Disorders, Postoperative Delirium, Postoperative Outcomes
    Trial name
    CREATE (NCT07310043)
    Testing
    Creatine monohydrate
    Volunteers
    120 people, healthy volunteers welcome
    Sponsor
    Massachusetts General Hospital
    Can I take part? CREATE
  • Cardiac Surgery With Cardiopulmonary Bypass, Postoperative Delirium

    Mechanisms and Intervention Strategies of Perioperative Glycemic Variability on Postoperative Delirium

    • Recruiting
    • Age: 18 years and older

    Delirium is a sudden change in attention, thinking, and awareness that can occur after heart surgery. It may slow recovery and is associated with longer hospital stays and poorer health outcomes.

    Trial name
    NCT07893353
    Testing
    Intranasal insulin-20U, Intranasal insulin-40U, Intranasal Saline
    Where
    China
    Volunteers
    225 people
    Sponsor
    Fujian Medical University Union Hospital
    Can I take part? NCT07893353
  • Implementation Science, Delirium

    Behavioral Economic & Staffing Strategies in the ICU

    • Recruiting
    • Age: 19 years and older
    • Lifestyle or therapy programme

    The overarching goal of this study is to support the "real world" assessment of strategies used to foster adoption of several highly efficacious evidence-based practices in healthcare systems that provide care to critically ill…

    Conditions
    Implementation Science, Delirium, Critical Illness, Mechanical Ventilation Complication
    Trial name
    BEST-ICU (NCT06184945)
    Testing
    Realtime audit and feedback, RN Implementation Facilitator
    Where
    3 sites in United States
    Volunteers
    16,500 people
    Sponsor
    University of Nebraska
    Can I take part? BEST-ICU
  • Postoperative Cognitive Complications, Delirium

    Prospective Observational Multimodal Neuromonitoring During High-Risk Adult Surgery

    • Not yet recruiting
    • Age: 18 years and older
    • Observational study

    This is a prospective observational cohort study of adult patients undergoing high-risk surgery at UT Southwestern Medical Center.

    Conditions
    Postoperative Cognitive Complications, Delirium, Perioperative/Postoperative Complications, Brain Injuries
    Trial name
    NCT07577726
    Where
    United States
    Volunteers
    300 people
    Sponsor
    University of Texas Southwestern Medical Center
    Can I take part? NCT07577726
  • Sleep, Circadian Dysregulation

    reALIGNing Circadian Rhythm and Promoting Sleep in the Intensive Care Unit

    • Not yet recruiting
    • Age: 18 years and older
    • Early Phase 1

    The goal of this pilot clinical trial is to learn whether a program to support sleep and the body's daily rhythms can be delivered safely and consistently to critically ill adults in intensive care units (ICUs).

    Conditions
    Sleep, Circadian Dysregulation, ICU, Delirium in Intensive Care Unit
    Trial name
    ALIGN ICU (NCT07886567)
    Testing
    Sleep chronobundle, Control
    Where
    Canada
    Volunteers
    50 people
    Sponsor
    University of Alberta
    Can I take part? ALIGN ICU
  • Emergence Agitation, Vocal Cord Polyps

    Intranasal Dexmedetomidine Combined With Esketamine for Emergence Quality After Suspension Laryngoscopy

    • Not yet recruiting
    • Age: 18 to 65 years

    This is a single-center, prospective, single-blinded, randomized controlled trial conducted at The First Hospital of Jilin University.

    Trial name
    NCT07880938
    Testing
    Dexmedetomidin, Esketamine
    Where
    China
    Volunteers
    134 people
    Sponsor
    The First Hospital of Jilin University
    Can I take part? NCT07880938
  • Postoperative Delirium (POD), Gynecologic Cancers

    Immunonutrition and Neuromonitoring for Postoperative Delirium in Gynecologic Oncology

    • Recruiting
    • Age: 65 to 80 years
    • Observational study

    Early postoperative delirium (POD) is a common and distressing neuropsychiatric complication frequently observed in elderly patients undergoing major surgical interventions, including radical and cytoreductive gynecologic…

    Conditions
    Postoperative Delirium (POD), Gynecologic Cancers, Malnutitrion
    Trial name
    NCT07877285
    Testing
    Preoperative Immunonutritional Scoring and Intraoperative Neuromonitoring
    Where
    Turkey (Türkiye)
    Volunteers
    80 people
    Sponsor
    Elazıg Fethi Sekin Sehir Hastanesi
    Can I take part? NCT07877285
  • Emergence Delirium, Post-Operative Cognitive Dysfunction

    Post Operative Cognitive Dysfunction After Oncologic Surgery

    • Recruiting
    • Age: 18 years and older
    • Observational study

    Aim of this trial is to define if Post-Operative Cognitive Dysfunction, detected analyzing changes between pre-operative and post-operative Neurocognitive Test, and Postoperative Delirium, relate to concentration of effector's…

    Trial name
    NCT03774420
    Where
    Italy
    Volunteers
    200 people
    Sponsor
    University of Padova
    Can I take part? NCT03774420

Completed, with results posted

All 99
  • Child, Intensive Care Unit Acquired Weakness

    Clinical Effectiveness of the "PICU Up!" Multifaceted Early Mobility Intervention for Critically Ill Children

    • Completed
    • Age: All ages
    • Results posted

    While mortality in U.S. pediatric intensive care units (PICUs) is improving, surviving children frequently develop persistent physical, cognitive, and psychological impairments.

    Conditions
    Child, Intensive Care Unit Acquired Weakness, Critical Illness, Hospital Acquired Pressure Ulcer
    Trial name
    PICU Up! (NCT04989790)
    Testing
    PICU Up!
    Where
    11 sites in United States
    Volunteers
    1,470 people
    Sponsor
    Johns Hopkins University
    Can I take part? PICU Up!
  • Postoperative Delirium, Sleep

    Minimizing ICU Neurological Dysfunction With Dexmedetomidine-induced Sleep

    • Completed
    • Age: 60 years and older
    • Phase 2/3
    • Results posted

    This study aims to determine whether, compared with placebo, the nighttime administration of a intravenous dexmedetomidine is effective at inducing sleep and preventing postoperative delirium in extubated post-cardiac surgical…

    Conditions
    Postoperative Delirium, Sleep, Anesthesia
    Trial name
    MINDDS (NCT02856594)
    Testing
    Dexmedetomidine
    Where
    United States
    Volunteers
    469 people, healthy volunteers welcome
    Sponsor
    Massachusetts General Hospital
    Can I take part? MINDDS
  • Thiamine Deficiency, Thiamine Deficiency; Sequelae

    Prevalence of Thiamine Deficiency in Hospitalized Non-Alcoholic Veterans

    • Completed
    • Age: 18 years and older
    • Observational study
    • Results posted

    Thiamine micronutrient deficiency (TD) can cause a variety of non-specific symptoms and leads to several thiamine deficiency disorders such as heart failure, polyneuropathy, Wernicke's Encephalopathy and generalized weakness and…

    Trial name
    NCT05480943
    Testing
    Thiamine repletion
    Where
    United States
    Volunteers
    206 people
    Sponsor
    VA Office of Research and Development
    Can I take part? NCT05480943
  • Weakness, Muscle, Delirium in Old Age

    YOOMI: Effect of Gamified Physical Therapy Exercise Software on Inpatient Mobility

    • Completed
    • Age: 65 years and older
    • Medical device
    • Results posted

    Patients admitted to the hospital often develop functional impairments due to being in bed most of the day. Each day of bedrest leads to significant muscle loss.

    Conditions
    Weakness, Muscle, Delirium in Old Age, Muscle Atrophy or Weakness, Muscle Loss
    Trial name
    YOOMI (NCT05815017)
    Testing
    Yoomi Physical Therapy Software
    Where
    United States
    Volunteers
    30 people, healthy volunteers welcome
    Sponsor
    Rutgers, The State University of New Jersey
    Can I take part? YOOMI
  • Postoperative Insomnia, Postoperative Delirium

    Efficacy of Suvorexant on Post-operative Sleep Disturbance

    • Completed
    • Age: 50 to 90 years
    • Phase 4
    • Results posted

    The study is a parallel group, double blind, randomized trial. Subjects will be recruited from individuals undergoing elective surgery for orthopedic, abdominal, urologic, gynecologic or spine reasons.

    Trial name
    NCT05823844
    Testing
    Suvorexant
    Where
    United States
    Volunteers
    100 people
    Sponsor
    Columbia University
    Can I take part? NCT05823844

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