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AzTrials

Research institution

Charles University, Czech Republic Clinical Trials

Studies where Charles University, Czech Republic is the lead sponsor: what is enrolling now, by phase, condition and country.

228 registered studies

In numbers

Open to volunteers
53
Active
61
With results posted
2
All registered
228

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

Open to volunteers

All 53
  • Urinary Incontinence , Stress, Laser Therapy

    Standardized 4D Transperineal Ultrasound Assessment of Urethrovesical Junction Mobility After Vaginal Laser Treatment for Stress Urinary Incontinence.

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

    This prospective single-center observational cohort study will assess changes in urethrovesical junction (UVJ) mobility and urethral morphology after vaginal Er:YAG laser treatment in 40 adult women with pure stress urinary…

    Trial name
    NCT07907016
    Where
    Czechia
    Volunteers
    40 people
    Sponsor
    Charles University, Czech Republic
    Can I take part? NCT07907016
  • Trauma, Brain

    Risk Assessment of Mild Traumatic Brain Injury in Military Training

    • Enrolling by invitation
    • Age: 18 to 50 years

    The SNIPER-TBI study aims to identify and quantify the risk of mild traumatic brain injury (mTBI) in soldiers of the Czech Armed Forces during specific high-risk training activities, including parachute jumps, high-caliber…

    Trial name
    NCT06992570
    Testing
    Quantification of mild trauma brain injury risk, Biomechanical Analysis of Head Impact Forces
    Where
    Czechia
    Volunteers
    50 people, healthy volunteers welcome
    Sponsor
    Charles University, Czech Republic
    Can I take part? NCT06992570
  • Leg Ulcer

    Topical Sevoflurane for Treatment of Chronic Leg Ulcers

    • Recruiting
    • Age: 18 years and older
    • Phase 4

    Patients with painful non-healing leg ulcer will be enrolled in the clinical single-blinded randomized study. The active treatment group will have sevoflurane applied at approximately 1 ml/cm2 at the start of wound treatment, the…

    Trial name
    NCT05303805
    Testing
    Sevoflurane, Cyteal
    Where
    Czechia
    Volunteers
    50 people
    Sponsor
    Charles University, Czech Republic
    Can I take part? NCT05303805
  • Obesity, Physical Inactivity

    Exercise Snacks Enabled by an mHealth Intervention Delivered in General Practice to Promote a Sustainable Active Lifestyle in Adults With Obesity

    • Not yet recruiting
    • Age: 18 to 65 years
    • Medical device
    • Lifestyle or therapy programme

    Adults with obesity gain as much from regular physical activity as anyone else, but structured exercise programmes are hard to sustain once the programme ends.

    Conditions
    Obesity, Physical Inactivity, Sedentary Behavior
    Trial name
    SnackFIT (NCT07867665)
    Testing
    Exercise snacks programme, Conversational agent, Wrist-worn activity tracker
    Where
    3 sites in Czechia
    Volunteers
    306 people
    Sponsor
    Charles University, Czech Republic
    Can I take part? SnackFIT
  • Vision Disorder, Stroke

    Visual Impairment and Functional Visual Performance Following Acquired Brain Injury: A Cross-Sectional Study

    • Enrolling by invitation
    • Age: 18 to 85 years
    • Observational study

    This cross-sectional observational study aims to characterize acquired visual impairment in adults with acquired brain injury and to examine the relationship between objectively identified visual impairment and self-reported…

    Conditions
    Vision Disorder, Stroke, Brain Injuries
    Trial name
    NCT07858708
    Where
    Czechia
    Volunteers
    108 people
    Sponsor
    Charles University, Czech Republic
  • Brain Injuries

    Pilot Study of Individualized Neurovisual Rehabilitation Following Acquired Brain Injury

    • Not yet recruiting
    • Age: 18 to 85 years
    • Lifestyle or therapy programme

    This prospective single-group pilot study will evaluate the feasibility and preliminary outcomes of an individualized neurovisual rehabilitation program for adults with visual impairment following acquired brain injury.

    Trial name
    NCT07849582
    Testing
    Individualized Neurovisual Rehabilitation
    Where
    Czechia
    Volunteers
    30 people
    Sponsor
    Charles University, Czech Republic
    Can I take part? NCT07849582
  • Ovarian Cancer, Ovarian Cancer Stage III

    Prehabilitation in Gynaecological Cancer Patients

    • Recruiting
    • Age: 18 to 85 years
    • Phase 3
    • Lifestyle or therapy programme

    Prehabilitation refers to interventions aiming to improve patients' resilience and functional capacity before a known stressful event, e.g., scheduled surgery.

    Conditions
    Ovarian Cancer, Ovarian Cancer Stage III, Ovarian Cancer Stage IV, Endometrial Cancer
    Trial name
    PHOCUS (NCT04789694)
    Testing
    Physiological intervention, Psychological intervention, Nutritional intervention
    Where
    Czechia
    Volunteers
    64 people
    Sponsor
    Charles University, Czech Republic
    Can I take part? PHOCUS
  • Atrial Fibrillation (AF)

    Extended Ablation Versus Pulmonary Vein Isolation to Treat Persistent Atrial Fibrillation

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

    The aim is to determine the effect of extended ablation (pre-specified linear PF/RF lesion set) in addition to PVI in symptomatic persistent AF patients on AF/AT/AFL recurrence.

    Trial name
    EXTEND-PVI (NCT07424326)
    Testing
    PVI-plus, PVI-only
    Where
    4 sites in Czechia
    Volunteers
    450 people
    Sponsor
    Charles University, Czech Republic
    Can I take part? EXTEND-PVI
  • Neonatology

    EXTERNAL NEGATIVE PRESSURE DURING LISA

    • Recruiting
    • Age: 1 hour to 3 days
    • Surgery or procedure

    The goal of this clinical trial is to evaluate the feasibility, safety, and preliminary effectiveness of applying external continuous negative pressure (ECNP) during less invasive surfactant administration (LISA) in preterm…

    Trial name
    ENCP LISA (NCT07271368)
    Testing
    ENCP
    Where
    Czechia
    Volunteers
    25 people
    Sponsor
    Charles University, Czech Republic
    Can I take part? ENCP LISA
  • Endometriosis, Endometriosis (Diagnosis)

    Deep Endometriosis Affecting the Urogenital Tract: Long-term Outcomes and Impact on Renal Function

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

    Endometriosis is a chronic estrogen-dependent disease characterized by the presence and growth of endometrium-like tissue outside the uterine cavity.

    Conditions
    Endometriosis, Endometriosis (Diagnosis), Urinary Tract Diseases
    Trial name
    RENDO (NCT07776574)
    Where
    Czechia
    Volunteers
    20 people
    Sponsor
    Charles University, Czech Republic
    Can I take part? RENDO

Completed, with results posted

All 2

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