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AzTrials

Drug or intervention

Experimental Group Clinical Trials

Studies that test Experimental Group, alone, with other treatments or as the comparison.

779 registered studies

In numbers

Open to volunteers
166
Active
199
With results posted
19
All registered
779

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

Open to volunteers

All 166
  • Pain, Chronic

    VR and Cooled Genicular Nerve Radio Frequency Ablation for Chronic Knee Pain

    • Recruiting
    • Age: 18 years and older

    This study will examine the impact of virtual reality used in conjunction with sedation compared to sedation alone in patients undergoing watervcooled genicular nerve ablations for chronic knee pain.

    Trial name
    NCT06336447
    Testing
    Experimental: Group #1: Virtual Reality Headset, Group 2 No Virtual Reality Headset
    Where
    United States
    Volunteers
    62 people
    Sponsor
    Northwestern University
    Can I take part? NCT06336447
  • Trauma, Psychological, Traumatic Stress Disorder

    Group Cognitive Processing Therapy for Women Survivors of Gender-Based Violence: Feasibility Study

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

    Introduction: Post-traumatic stress disorder (PTSD) is a global health challenge requiring effective, evidence-based interventions, such as Cognitive Processing Therapy (CPT).

    Trial name
    HEALING-TRAUMA (NCT07897903)
    Testing
    Group CPT + TAU (Experimental)
    Volunteers
    10 people
    Sponsor
    Universidad Complutense de Madrid
  • Breast Cancer, HER2-negative Breast Cancer

    Albumin-Bound Paclitaxel (Ⅱ) in Patients With Advanced Breast Cancer

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

    This is a multicenter, prospective, observational real-world study. The study aims to evaluate the efficacy, safety and economic benefits of albumin-bound paclitaxel (Ⅱ) compared with conventional albumin-bound paclitaxel, in…

    Conditions
    Breast Cancer, HER2-negative Breast Cancer, Advanced Breast Cancer
    Trial name
    NCT07899047
    Testing
    Experimental Group, control group
    Where
    China
    Volunteers
    1,372 people
    Sponsor
    Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
    Can I take part? NCT07899047
  • Multiple Sclerosis

    Evaluation of the Effect of Mental Imagery Training Combined With Modified Constraint-Induced Movement Therapy in Individuals With Multiple Sclerosis

    • Not yet recruiting
    • Age: All ages
    • Lifestyle or therapy programme

    This study aims to investigate the effects of mental imagery training combined with modified constraint-induced movement therapy in individuals with multiple sclerosis.

    Trial name
    NCT07899411
    Testing
    odified Constraint-Induced Movement Therapy + Mental Imagery Training, Modified Constraint-Induced Movement Therapy
    Where
    Turkey (Türkiye)
    Volunteers
    14 people
    Sponsor
    Hacettepe University
    Can I take part? NCT07899411
  • Osteosarcoma, Pediatric Osteosarcoma

    Fight Osteosarcoma Through European Research Evolving Study Platform From Diagnosis to Relapse

    • Recruiting
    • Age: 4 years and older
    • Phase 3
    • Pill or oral medicine

    This clinical study is the initiative of the FOSTER (Fight OsteoSarcoma Through European Research) consortium and Gustave Roussy, which is the sponsor.

    Conditions
    Osteosarcoma, Pediatric Osteosarcoma, Osteosarcoma in Children, Osteosarcoma in Adolescents and Young Adults
    Trial name
    FOSTER (NCT07871864)
    Testing
    Experimental group : Cabometyx ® 40mg/m2/day (Max: 60mg/day) , Treatment schedule : Daily**, day 1-28 during 4 weeks (ie. 1 cycle) during 12 cycles
    Where
    77 sites in Denmark, Finland and 6 more
    Volunteers
    530 people
    Sponsor
    Gustave Roussy, Cancer Campus, Grand Paris
    Can I take part? FOSTER
  • Diabetes Mellitus, Peripheral Arterial Disease

    Construction and Empirical Research of a Risk Prediction Model for Preventing Lower Extremity Arteriosclerosis Obliterans in Diabetic Patients Based on the HAPA Model

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

    In this study, Logistic regression analysis was used to construct a risk prediction model for ASO in diabetic patients. Guided by the HAPA model, a nursing intervention plan for preventing ASO in diabetic patients was constructed…

    Trial name
    NCT07881588
    Testing
    Routine Care, Experimental group intervention
    Where
    China
    Volunteers
    154 people
    Sponsor
    Second Affiliated Hospital of Nanchang University
    Can I take part? NCT07881588
  • Upper Cross Syndrome, Spinal Alignment

    Beyond Osteopathic Therapy: Functional Performance Following the Addition of Ujjayi Pranayama in College Students With Upper Cross Syndrome

    • Recruiting
    • Age: 20 to 29 years

    This study aims to explore the relationship between spinal alignment and functional performance in individuals with upper cross syndrome following a combined breathing and manual therapy program.

    Conditions
    Upper Cross Syndrome, Spinal Alignment, Functional Performance
    Trial name
    NCT07786415
    Testing
    The experimental group will perform ujjayi pranayama and osteopathic manipulative tratment, control group will perform osteopathic manipulative treatment only
    Where
    Egypt
    Volunteers
    40 people
    Sponsor
    Al-Zaytoonah University of Jordan
    Can I take part? NCT07786415
  • Small-cell Lung Cancer, Brain Metastases

    SRS/SRT/Hypo-RT Versus HA-WBRT for No More Than 10 Brain Metastases in SCLC

    • Recruiting
    • Age: 18 to 80 years
    • Phase 3
    • Surgery or procedure

    This phase III trial compares the effect of stereotactic radiosurgery and whole brain radiation therapy that avoids the hippocampus (the memory zone of the brain) for the treatment of small cell lung cancer that has spread to the…

    Conditions
    Small-cell Lung Cancer, Brain Metastases, SRS, Stereotactic Radiotherapy
    Trial name
    SHARP (NCT06457906)
    Testing
    Experimental group (SRS/SRT/Hypo-RT), Controled group (HA-WBRT)
    Where
    China
    Volunteers
    340 people
    Sponsor
    Cancer Institute and Hospital, Chinese Academy of Medical Sciences
    Can I take part? SHARP
  • Pregnant Women

    Performance and Safety of Assisted Vaginal Delivery With the Odon Device™ Versus Vacuum Extraction

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

    This is a pivotal study designed to demonstrate the non-inferiority of the Odon Device™ versus vacuum extraction

    Trial name
    E-SAFE-ODON (NCT07862842)
    Testing
    Experimental: The BD Odon DeviceTM, Active Comparator: Vacuum extraction group
    Volunteers
    628 people
    Sponsor
    Centre Hospitalier Universitaire de Besancon
  • Opioid Use Disorder, Opioid Overdose

    A Bundled Intervention to End Opioid Overdoses

    • Recruiting
    • Age: 19 years and older
    • Phase 4
    • Pill or oral medicine
    • Lifestyle or therapy programme

    Opioid overdose deaths have reached historically high records in the United States and are particularly concentrated among patients after emergency department (ED) discharge.

    Trial name
    B-CARE (NCT07485335)
    Testing
    Bundled intervention (Experimental), control group, Buprenorphine (Experimental)
    Where
    United States
    Volunteers
    160 people
    Sponsor
    University of Alabama at Birmingham
    Can I take part? B-CARE

Completed, with results posted

All 1,020
  • Orthodontic Tooth Movement

    Clinical Trial to Assess the Efficacy of Reducing the Aligners' Wear Protocol

    • Completed
    • Age: 18 to 30 years
    • Medical device
    • Results posted

    The hypothesis of this project is that replacing the current 7-day wear protocol with a 3-day wear protocol, while integrating less tooth movement per aligner (reduce the amount of activation per aligner) may produce more…

    Trial name
    NCT05905224
    Testing
    Invisalign 7-day wear protocol, Invisalign 3-day wear protocol
    Where
    United States
    Volunteers
    45 people, healthy volunteers welcome
    Sponsor
    University of Florida
    Can I take part? NCT05905224
  • Opioid Use Disorder, Opioid Overdose

    A Bundled Intervention

    • Completed
    • Age: 19 years and older
    • Phase 4
    • Results posted

    Opioid overdose deaths have reached historically high records in the United States and are particularly concentrated among patients after emergency department (ED) discharge.

    Trial name
    B-CARE (NCT06593093)
    Testing
    a bundled intervention, including peer support specialist, buprenorphine, physician care, and telehealth
    Where
    United States
    Volunteers
    30 people
    Sponsor
    University of Alabama at Birmingham
    Can I take part? B-CARE
  • Mild Cognitive Impairment, Adherence, Patient

    MI-CBT Adherence Program for Lifestyle Interventions in Older Adults

    • Completed
    • Age: 60 to 85 years
    • Lifestyle or therapy programme
    • Results posted

    Objective 1: Assess feasibility and acceptability of all protocol components of a pilot trial testing a 6-week telehealth Mediterranean ketogenic nutrition adherence (KNA) program using motivational interviewing and cognitive…

    Conditions
    Mild Cognitive Impairment, Adherence, Patient, Ketosis
    Trial name
    MI-CBT KNAP (NCT04817176)
    Testing
    Motivational Interviewing-Cognitive Behavioral Therapy Ketogenic Nutrition Adherence Program, Ketogenic Nutrition Program
    Where
    United States
    Volunteers
    58 people, healthy volunteers welcome
    Sponsor
    Florida State University
    Can I take part? MI-CBT KNAP
  • Acne

    Efficacy and Safety of IDP-121 and IDP-121 Vehicle Lotion in the Treatment of Participants With Acne Vulgaris

    • Completed
    • Age: 9 years and older
    • Phase 3
    • Results posted

    The objective of this study was to evaluate the efficacy, safety, and tolerability of a once daily topical application of IDP-121 Lotion compared with its vehicle (IDP-121 Vehicle Lotion) in participants with moderate to severe…

    Trial name
    NCT02932306
    Testing
    IDP-121 Lotion, IDP-121 Vehicle Lotion
    Where
    39 sites in United States
    Volunteers
    820 people
    Sponsor
    Bausch Health Americas, Inc.
    Can I take part? NCT02932306
  • Chronic Conditions, Multiple

    ElderTree Via a Voice Activated Device for Managing Chronic Health Conditions (NHLBI)

    • Completed
    • Age: 60 years and older
    • Lifestyle or therapy programme
    • Results posted

    Multiple chronic conditions (MCCs) are costly and pervasive among older adults. MCCs account for 90% of Medicare spending, and 65% of Medicare beneficiaries have 3 or more chronic conditions; 23% have 5 or more.

    Trial name
    NCT05240534
    Testing
    ET-Text (Laptop), ET-Voice (Smart System)
    Where
    United States
    Volunteers
    502 people
    Sponsor
    University of Wisconsin, Madison
    Can I take part? NCT05240534

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