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AzTrials

Drug or intervention

Routine care Clinical Trials

Studies that test Routine care, alone, with other treatments or as the comparison.

639 registered studies

In numbers

Open to volunteers
202
Active
218
With results posted
23
All registered
639

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

Open to volunteers

All 202
  • Renal Cell Carcinoma, Urothelial Carcinoma

    Registry Platform Urologic Cancer

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

    The purpose of the project is to set up a national, prospective, longitudinal, multicenter cohort study with associated satellites, a tumor registry platform, to document uniform data on characteristics, molecular diagnostics…

    Trial name
    CARAT (NCT03374267)
    Testing
    Routine care as per site standard.
    Where
    Germany
    Volunteers
    2,230 people
    Sponsor
    iOMEDICO AG
    Can I take part? CARAT
  • Prematurity, Feeding Behaviors

    Effects of Environmental Comfort and Oral Motor Stimulation on Comfort and Oral Feeding Readiness in Preterm Infants

    • Not yet recruiting
    • Age: 1 hour to 12 months
    • Pill or oral medicine
    • Lifestyle or therapy programme

    This study aims to evaluate the effects of short-term environmental comfort interventions and oral motor stimulation on comfort and oral feeding readiness in preterm infants.

    Trial name
    NCT07917871
    Testing
    Massage, White Noise, Oral Motor Stimulation
    Where
    Turkey (Türkiye)
    Volunteers
    84 people
    Sponsor
    Marmara University
  • Intensive Care Unit Acquired Weakness

    Blood Flow Restriction Training for Mechanically Ventilated Patients With ICU-Acquired Weakness

    • Recruiting
    • Age: 18 to 75 years

    Patients receiving mechanical ventilation in the intensive care unit (ICU) frequently develop ICU-acquired weakness - a condition marked by widespread muscle loss and weakness caused by prolonged bed rest, severe illness, and…

    Trial name
    BFRT-ICU (NCT07802743)
    Testing
    Blood flow restriction training, Standard ICU Care and Routine Rehabilitation
    Where
    China
    Volunteers
    120 people
    Sponsor
    Affiliated Hospital of Jining Medical University
    Can I take part? BFRT-ICU
  • Breast Neoplasm Malignant Primary, Lymphedema Arm

    Agentic AI App and Home Bioimpedance Monitoring for Endocrine Therapy Adherence and Lymphedema in Breast Cancer Survivors

    • Not yet recruiting
    • Age: 18 to 75 years
    • Medical device
    • Lifestyle or therapy programme

    As survival rates following breast cancer surgery continue to improve, long-term survivorship management has emerged as a crucial clinical priority.

    Conditions
    Breast Neoplasm Malignant Primary, Lymphedema Arm, Medication Adherence, Ductal Carcinoma In Situ
    Trial name
    Pinkmate (NCT07911839)
    Testing
    Cohort1: Pinkmate Agentic AI-ePRO Active Management Platform, Cohort1: Pinkmate Basic Medication Reminders and Standard Outpatient Care, Cohort2: InBody BWA ON Home Bioimpedance Monitoring and Behavioral App
    Where
    South Korea
    Volunteers
    264 people
    Sponsor
    Chang-Ik Yoon
    Can I take part? Pinkmate
  • Chronic Coronary Syndrome

    Out-Patient Proactive Observation With Wearable-Assisted Tracking for Cardiovascular Health Management

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

    The goal of this randomized controlled study is to evaluate whether a wearable device-based, Life's Essential 8 (LE8)-guided management strategy can improve cardiovascular health in patients with chronic coronary syndrome (CCS).

    Trial name
    OPPO-WATCH (NCT07912671)
    Testing
    Wearable Device-Based Monitoring and LE8 Feedback, Routine Outpatient Care With Data-Blinded Wearable Monitoring
    Where
    China
    Volunteers
    400 people
    Sponsor
    China National Center for Cardiovascular Diseases
    Can I take part? OPPO-WATCH
  • Breastfeeding Rates

    Development and Implementation of a Breastfeeding Program for Post-Cesarean Section Women Based on the 5A Nursing Model

    • Enrolling by invitation
    • Age: 18 to 50 years
    • Lifestyle or therapy programme

    Develop and apply a breastfeeding program for postoperative mothers of cesarean section based on the 5A nursing model, and evaluate its impact on the mothers' mastery of breastfeeding knowledge, self-efficacy, breastfeeding rate…

    Trial name
    NCT07913438
    Testing
    Based on the 5A nursing intervention plan, Implement routine care
    Where
    China
    Volunteers
    60 people
    Sponsor
    The Third Xiangya Hospital of Central South University
  • Depressive Symptoms, Perinatal Loss

    e-Perinatal Butterfly: An Embedded Study for Parents Experiencing Perinatal Loss

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

    This study is part of the e-Perinatal project and is embedded within the parent e-Perinatal cluster randomized controlled trial (NCT07613008). No additional randomization is performed for this embedded study.

    Conditions
    Depressive Symptoms, Perinatal Loss, Perinatal Grief, Anxiety Symptoms
    Trial name
    e-Butterfly (NCT07898176)
    Testing
    e-Perinatal Butterfly, Standard routine maternal care
    Volunteers
    60 people, healthy volunteers welcome
    Sponsor
    University of Seville
    Can I take part? e-Butterfly
  • HIV, HIV - Human Immunodeficiency Virus

    Bwelela Easy Study

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

    Treatment interruption in HIV care is one of the most enduring challenges to HIV programs globally and is associated with high rates of detectable virus in the blood and overall morbidity and mortality.

    Conditions
    HIV, HIV - Human Immunodeficiency Virus, Treatment Interruption, Reengagement
    Trial name
    NCT07900750
    Testing
    Standard of Care - Routine Phone Outreach / Standard of Care - Routine Care and Counseling (SOC-RPO/SOC-RCC), Standard of Care - Routine Phone Outreach / Navigation (SOC-RPO/NAV), Standard of Care - Routine Phone Outreach / Navigation plus Community-Based Medication Delivery (SOC-RPO/NAV+CB-Med)
    Where
    Zambia
    Volunteers
    1,500 people
    Sponsor
    Washington University School of Medicine
    Can I take part? NCT07900750
  • Hepatic Encephalopathy, Liver Cirrhosis

    Effect of Mini-Program Monitoring on Hepatic Encephalopathy in Post-TIPS Patients

    • Not yet recruiting
    • Age: 18 to 75 years
    • Medical device

    This study is a prospective, multicenter, randomized controlled clinical trial. It aims to evaluate whether an early monitoring and warning system based on a smartphone mini-program can effectively reduce the incidence of overt…

    Trial name
    NCT07901556
    Testing
    Standard Care and Routine Follow-Up, Hepatic Encephalopathy Intelligent Monitoring Mini-Program
    Volunteers
    394 people
    Sponsor
    The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School
    Can I take part? NCT07901556
  • Adolescent Idiopathic Scoliosis (AIS)

    Protocol for a Randomized Controlled Trial of a Clinician-Supervised Home-School-Hospital-Linked Digital Health Platform-Supported Conservative Management Pathway for AIS

    • Recruiting
    • Age: 12 to 16 years
    • Lifestyle or therapy programme

    Adolescent idiopathic scoliosis (AIS) brings substantial physical and psychological burden to affected teenagers, and current conservative follow-up management is fragmented under routine clinical settings.

    Trial name
    NCT06314594
    Testing
    Routine Guideline-Based Conservative Care, Clinician-Supervised, Platform-Assisted Conservative Management
    Where
    China
    Volunteers
    76 people
    Sponsor
    Hangzhou Medical College
    Can I take part? NCT06314594

Completed, with results posted

All –
  • Abdominal (ABD) Infection

    INSPIRE Trial for Abdominal Infections

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

    The INSPIRE Abdominal Infection Trial is a cluster-randomized controlled trial of HCA Healthcare hospitals comparing routine empiric antibiotic stewardship practices with real-time, precision medicine computerized physician order…

    Trial name
    NCT05423743
    Testing
    Arm 1: Routine Care, Arm 2: INSPIRE Stewardship Bundle for Abdominal Infection
    Where
    101 sites in United States
    Volunteers
    198,480 people
    Sponsor
    Harvard Pilgrim Health Care
    Can I take part? NCT05423743
  • Skin and Soft Tissue (SST) Infection

    INSPIRE Trial for Skin and Soft Tissue Infections

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

    The INSPIRE Skin and Soft Tissue Infection trial is a cluster-randomized controlled trial of HCA Healthcare hospitals comparing routine empiric antibiotic stewardship practices with real-time, precision medicine computerized…

    Trial name
    NCT05423756
    Testing
    Arm 1: Routine Care, Arm 2: INSPIRE Stewardship Bundle for Skin and Soft Tissue Infection
    Where
    102 sites in United States
    Volunteers
    118,562 people
    Sponsor
    Harvard Pilgrim Health Care
    Can I take part? NCT05423756
  • PreDiabetes

    CGM Plus GEM in Prediabetes

    • Completed
    • Age: 25 to 70 years
    • Lifestyle or therapy programme
    • Results posted

    This study is designed to look into the effect of a lifestyle management guide called GEM (Glycemic Excursion Minimization) alongside continuous glucose monitoring (CGM) and an activity monitor (FitBit) and the effect this can…

    Trial name
    IMPEDE (NCT05580978)
    Testing
    GEM, Routine Care
    Where
    United States
    Volunteers
    61 people
    Sponsor
    University of Colorado, Denver
    Can I take part? IMPEDE
  • Epilepsy

    Bridging the Childhood Epilepsy Treatment Gap in Africa

    • Completed
    • Age: 6 months to 16 years
    • Results posted

    About half of the world's children with epilepsy do not receive treatment - known as the epilepsy treatment gap - with significantly higher rates (67%-90%) in low- and middle-income countries (LMICs).

    Trial name
    BRIDGE (NCT04290975)
    Testing
    Task-shifting epilepsy care to epilepsy-trained community health workers (CHWs), Enhanced usual care for epilepsy (EUC)
    Where
    3 sites in Nigeria
    Volunteers
    1,672 people
    Sponsor
    Vanderbilt University Medical Center
    Can I take part? BRIDGE
  • Thyroid Nodules, Thyroid Cancer

    AIM2: Adequate Selection of Patients for Thyroid Biopsy: Evaluation of a Shared Decision Making Conversation Aid

    • Completed
    • Age: 18 to 99 years
    • Lifestyle or therapy programme
    • Results posted

    There is an epidemic of thyroid cancer that is harmful to patients and the medical system. The study hypothesizes that the use of an electronic conversation aid during clinical visits can help patients and clinicians collaborate.

    Trial name
    NCT04463719
    Testing
    Counseling using the electronic conversation aid, counseling by routine care
    Where
    2 sites in United States
    Volunteers
    107 people
    Sponsor
    University of Florida
    Can I take part? NCT04463719

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