Clinical trials: Functional Recovery, open to volunteers
Sepsis, Post Intensive Care Unit Syndrome
Accelerating Recovery After ICU Admission: Post-discharge Supplementation With Pasteurized Akkermansia Muciniphila.
The goal of this clinical trial is to learn if daily oral supplementation with pasteurized Akkermansia muciniphila (PAM), an EFSA-approved food supplement, can support recovery in adults who have recently been treated in the ICU…
- Conditions
- Sepsis, Post Intensive Care Unit Syndrome, Critical Illness, Microbiome Dysbiosis
- Trial name
- PAM-ICU (NCT07295353)
- Testing
- Pasteurized Akkermansia muciniphila
- Volunteers
- 50 people
- Sponsor
- Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Stroke
Power Exercise for Stroke Recovery: The POWER Pilot Trial (POWER-P)
Weakness is one of the most common consequences of stroke. For the over 750,000 Canadians living with stroke, many daily activities like standing from a chair, walking and balance not only require strength but often efforts in…
- Trial name
- POWER-P (NCT06780995)
- Testing
- Power Exercise for Stroke Recovery (POWER), Strength Training Engaging Guidelines to Enhance Total Health (STRENGTH)
- Where
- 2 sites in Canada
- Volunteers
- 60 people
- Sponsor
- McMaster University
Lumber Disc Prolapse
H-Reflex-Guided Direction-Sensitive Exercise Versus Standard Extension Exercise for Functional Recovery in Patients With Lumbar Disc Prolapse
This randomized controlled trial will compare H-reflex-guided direction-sensitive exercise with standard extension exercise in patients with lumbar disc prolapse.
- Trial name
- NCT07871422
- Testing
- H-Reflex-Guided Direction-Sensitive Exercise, Standard Lumbar Extension Exercise
- Where
- Egypt
- Volunteers
- 60 people
- Sponsor
- Delta University for Science and Technology
High Myopia
Comparison of Retinal Damage in ICL Implantation Using 3D Visualization System vs. Microscope
Implantable collamer lens (ICL) implantation is considered one of the most effective surgical treatments for high myopia. The procedure primarily involves adjusting the position of the ICL within the eye.
- Trial name
- NCT06966622
- Testing
- 3D visualization system with coaxial illumination, microscope with standard illumination
- Volunteers
- 40 people
- Sponsor
- Fuzhou Eye Hospital
Effect of Resveratrol on Performance and Recovery
Effect of Resveratrol Supplementation on Exercise Performance and Recovery
To examine the effects of once daily supplementation with 500mg VeriSperse® resveratrol (VRES) for 17 days on muscle function, delayed onset muscle soreness, systemic concentrations of muscular damage markers and markers of…
- Trial name
- NCT06723119
- Testing
- Resveratrol (VRES) 500 mg oral once daily.
- Where
- United States
- Volunteers
- 20 people, healthy volunteers welcome
- Sponsor
- University of Central Florida
Non Traumatic Spinal Cord Injury, Sub-Acute Rehabilitation
Functional Electrical Stimulation vs Transcutaneous Stimulation in Patients With Subacute Spinal Cord Injury
Cervical spinal cord injuries (SCI) are the most common form of spinal cord injuries within the veteran population. Losing arm function is a major concern with these injuries.
- Conditions
- Non Traumatic Spinal Cord Injury, Sub-Acute Rehabilitation, Spinal Cord Injury Cervical, Electric Stimulation Therapy
- Trial name
- NCT07911657
- Testing
- RTI Xcite, ExaStim
- Where
- United States
- Volunteers
- 20 people
- Sponsor
- Center for Veterans Research and Education
Spinal Cord Injuries, Neuromodulation
Harnessing Neuroplasticity of Postural Sensorimotor Networks Using Non-Invasive Spinal Neuromodulation to Maximize Functional Recovery After Spinal Cord Injury
It has been demonstrated that the human lumbosacral spinal cord can be neuromodulated with epidural (ESS) and transcutaneous (TSS) spinal cord stimulation to enable recovery of standing and volitional control of the lower limbs…
- Trial name
- NCT06213012
- Testing
- Transcutaneous Spinal cord Stimulation, Epidural Spinal Stimulation (ESS)
- Where
- United States
- Volunteers
- 60 people
- Sponsor
- The Methodist Hospital Research Institute
Aortic Valve Stenosis, Iron Deficiency
Iron Infusion in Patients Undergoing Transcatheter Aortic Valve Implantation
The aim of the open-label, randomized controlled superiority IRON TAVI trial is to investigate whether intravenous iron therapy (ferric carboxymaltose) improves Health-Related Quality of Life (HRQOL) in patients with severe…
- Conditions
- Aortic Valve Stenosis, Iron Deficiency, TAVI(Transcatheter Aortic Valve Implantation), Cardiovascular Diseases
- Trial name
- IRON TAVI (NCT07370688)
- Testing
- Intravenous ferric carboxymaltose
- Where
- Netherlands
- Volunteers
- 402 people
- Sponsor
- Erasmus Medical Center
Osteoarthritis of Knee
Preoperative Rehabilitation Training and Total Knee Arthroplasty Outcomes
Joint replacement surgery is an effective treatment for severe joint diseases, but the postoperative recovery process is complex and lengthy.
- Trial name
- PRTKAO (NCT06983912)
- Testing
- Preoperative Rehabilitation Training
- Volunteers
- 500 people
- Sponsor
- Fuzhou University Affiliated Provincial Hospital