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Beth Israel Deaconess Medical Center Clinical Trials

Studies where Beth Israel Deaconess Medical Center is the lead sponsor: what is enrolling now, by phase, condition and country.

567 registered studies

In numbers

Open to volunteers
79
Active
110
With results posted
172
All registered
567

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

Open to volunteers

All 79
  • Healthy

    Meditation and Yogic Breathing-driven Modulation of Neurofluid Coupling and Brain Clearance

    • Not yet recruiting
    • Age: 25 to 60 years
    • Lifestyle or therapy programme

    This study will examine whether meditation and yogic breathing can alter brain fluid movement and waste clearance in healthy adults.

    Trial name
    SPANDHA (NCT07903688)
    Testing
    Nadi Shuddhi, Shoonya Meditation
    Where
    United States
    Volunteers
    120 people, healthy volunteers welcome
    Sponsor
    Beth Israel Deaconess Medical Center
    Can I take part? SPANDHA
  • Hip Fractures (ICD-10 72.01-72.2), Post Operative Analgesia

    Suzetrigine (Journavx) as Multimodal Therapy for Pain Management in Adults Undergoing Surgery for Hip Fracture

    • Not yet recruiting
    • Age: 18 years and older
    • Phase 4

    The goal of this clinical trial is to learn whether suzetrigine (Journavx®), when added to standard multimodal pain management, can reduce opioid use while providing adequate pain control in adults undergoing surgery for an acute…

    Trial name
    STRIDE-HIP (NCT07905404)
    Testing
    Suzetrigine (Journavx)
    Where
    United States
    Volunteers
    79 people
    Sponsor
    Beth Israel Deaconess Medical Center
    Can I take part? STRIDE-HIP
  • Robotic Surgery

    Perioperative High-flow Nasal Oxygen in Patients Undergoing Robotic Surgery

    • Not yet recruiting
    • Age: 18 years and older
    • Medical device

    The aim of the study is to assess whether perioperative use of high-flow nasal oxygen (HFNO) during the period from induction of anesthesia until discharge from the post-anesthesia care unit in patients undergoing…

    Trial name
    Periop HFNO (NCT07591610)
    Testing
    High flow nasal oxygen
    Where
    United States
    Volunteers
    190 people
    Sponsor
    Beth Israel Deaconess Medical Center
    Can I take part? Periop HFNO
  • History Taking, Artificial Intelligence (AI)

    Safety, Feasibility, and Acceptability of the MINERVA Voice Conversational Agent for Emergency Department History-Taking

    • Enrolling by invitation
    • Age: 18 years and older
    • Observational study

    This study evaluates whether an artificial intelligence (AI) conversational agent called MINERVA (Medical Interface for Navigating the Emergency Room with Voice Assistance) can safely and feasibly gather medical histories from…

    Trial name
    MINERVA-HX (NCT07877883)
    Testing
    MINERVA AI Chatbot
    Where
    United States
    Volunteers
    250 people
    Sponsor
    Beth Israel Deaconess Medical Center
    Can I take part? MINERVA-HX
  • Neurotoxicity, Neurotoxicity Syndromes

    Assessing DCog Short for Neurotoxicity in CAR-T

    • Recruiting
    • Age: 18 years and older
    • Lifestyle or therapy programme

    The aim of this study is to determine the effectiveness of DCog Short, a self-reporting, iPad-based application tool, in assessing neurotoxicity in participants undergoing CAR-T cell therapy.

    Conditions
    Neurotoxicity, Neurotoxicity Syndromes, Hematologic Malignancy, Immune Effector Cell Associated Neurotoxicity Syndrome
    Trial name
    NCT07403812
    Testing
    DCog Short
    Where
    United States
    Volunteers
    40 people
    Sponsor
    Beth Israel Deaconess Medical Center
  • Labor Pain and to Reduce Pain

    Does the Volume of Medication Affect the Success of Labor Epidural Analgesia

    • Not yet recruiting
    • Age: 18 to 50 years
    • Phase 4

    The purpose of this study is to evaluate whether changing the volume and concentration of a medication affects the quality of pain relief and the side effects associated with labor epidural analgesia.

    Trial name
    EpiVol (NCT07684365)
    Testing
    administration of bupivacaine 7.5 mg and fentanyl 24 mcg every 40 minutes
    Volunteers
    70 people
    Sponsor
    Beth Israel Deaconess Medical Center
    Can I take part? EpiVol
  • Perioperative/Postoperative Complications, Postoperative Cognitive Dysfunction

    CEReBral AutorEgulation in Non-cardiac SuRgery and Relationship to Postoperative DeliriUm State

    • Recruiting
    • Age: 60 years and older
    • Observational study

    The goal of this observational study is to learn the how to determine the mean arterial pressure(MAP) or blood pressure level to be maintained during non-cardiac surgery for optimal brain health in patients above the age of 60…

    Conditions
    Perioperative/Postoperative Complications, Postoperative Cognitive Dysfunction, Postoperative Delirium, EEG With Periodic Abnormalities
    Trial name
    CERBERUS (NCT06133842)
    Testing
    Intra-op EEG and CO data collection
    Where
    United States
    Volunteers
    100 people, healthy volunteers welcome
    Sponsor
    Beth Israel Deaconess Medical Center
    Can I take part? CERBERUS
  • Chronic Obstructive Pulmonary Disease, Chronic Heart Failure

    Mindful Steps 2.0: Promoting Physical Activity in Patients With COPD and HF

    • Recruiting
    • Age: 40 years and older
    • Lifestyle or therapy programme

    The goal of this fully-remote randomized controlled trial is to test the efficacy of Mindful Steps in facilitating physical activity compared to usual standard of care among 136 patients with COPD and/or HF.

    Trial name
    NCT05934565
    Testing
    Mindful Steps
    Where
    2 sites in United States
    Volunteers
    136 people
    Sponsor
    Beth Israel Deaconess Medical Center
    Can I take part? NCT05934565
  • Artificial Intelligence (AI), Clinical Reasoning

    Teaching Doctors in Training to Reason With Artificial Intelligence

    • Enrolling by invitation
    • Age: All ages

    The purpose of the TEACH-AI study is to assess whether a brief, structured workshop on artificial intelligence can improve the performance of medicine doctors in training (i.e.

    Conditions
    Artificial Intelligence (AI), Clinical Reasoning, Clinical Decision-making, Medical Education
    Trial name
    TEACH-AI (NCT07813754)
    Testing
    Workshop-First
    Where
    4 sites in United States
    Volunteers
    200 people, healthy volunteers welcome
    Sponsor
    Beth Israel Deaconess Medical Center
    Can I take part? TEACH-AI
  • Women in the Menopausal Period

    ROSA-B: ALAN Exposure and Brain Health in Midlife Women With VMS

    • Not yet recruiting
    • Age: 45 to 58 years
    • Lifestyle or therapy programme

    This randomized, parallel-group study will examine how artificial light exposure during nighttime awakenings affects sleep and brain health in midlife women experiencing vasomotor symptoms, such as hot flashes and night sweats.

    Trial name
    NCT07834944
    Testing
    Artificial Light at Night (ALAN) 100 lux, Artificial Light at Night (ALAN) Dim Light
    Volunteers
    66 people, healthy volunteers welcome
    Sponsor
    Beth Israel Deaconess Medical Center
    Can I take part? NCT07834944

Completed, with results posted

All 133

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