Clinical Trials Logo

Atrophy clinical trials

View clinical trials related to Atrophy.

Filter by:
  • Not yet recruiting  
  • Page 1 ·  Next »

NCT ID: NCT06461286 Not yet recruiting - Clinical trials for Autosomal Dominant Optic Atrophy

SAD of IVT PYC-001 in OPA1 Mutation-Associated Autosomal Dominant Optic Atrophy (Sundew)

Start date: July 2024
Phase: Phase 1
Study type: Interventional

A First-in-Human multi-centre, prospective, Phase1a, Single Ascending Dose (SAD) interventional study of PYC-001 in participants with confirmed OPA1 mutation (haploinsufficiency) associated ADOA.

NCT ID: NCT06446687 Not yet recruiting - Clinical trials for Implant Site Reaction

Radiographic Assessment of Bone Gain Following Sinus Lifting With Simultaneous Implant Placement Using Crestal Approach With Membrane Control Technique for Bone Augmentation of Atrophied Maxillary Posterior Ridge

Start date: June 1, 2024
Phase: N/A
Study type: Interventional

This study aims to evaluate the quantity and quality of the native and the newly bone around dental implants that's simultaneously installed with sinus lifting

NCT ID: NCT06435884 Not yet recruiting - Atrophic Scar Clinical Trials

Long-Term Follow-up of Adult With Atorpphic Scars Treated With TRTP-101

Start date: September 2024
Phase:
Study type: Observational

CIC101-01-LT is a long-term follow-up study of subjects treated with TRTP-101 and will evaluate the long-term safety and efficacy of TRTP-101.

NCT ID: NCT06400316 Not yet recruiting - Clinical trials for Rheumatoid Arthritis

Muscle Wasting and Rheumatoid Arthritis Flares

Start date: May 13, 2024
Phase: N/A
Study type: Interventional

People living with Rheumatoid Arthritis (RA) often present with low muscle mass compared to their healthy counterparts. This affects their mobility, overall health and quality of life. Even though low muscle mass in RA has been recognised for decades, it is still highly prevalent and very little is known about its development, progression, and potential management. The researchers hypothesise that flares of disease activity trigger acute events of muscle wasting due to high inflammation and reduced mobility. This is commonly observed in bed rest studies and people hospitalised for various reasons. If this holds true for RA, it would point towards a stepwise development of RC and potentially allow for time-targeted management of it. A potential method to manage it is through the use of nutritional supplements. Specifically, amino acid supplementation (commonly used by athletes or people wanting to increase muscle mass) during and shortly after a flare may counteract some of the muscle wasting and allow for better long-term mobility and quality of life for people living with RA. This study aims to investigate aspects of muscle health changes following a disease flare-up in people with Rheumatoid Arthritis (RA) and test potential interventions to minimise any such changes. The investigators will randomly assign participants to a standard care or a nutritional supplementation group and assess aspects of body composition, muscle health, disease activity and inflammation on five occasions over a 3-month period.

NCT ID: NCT06396325 Not yet recruiting - Clinical trials for Spinal Muscular Atrophy

A Registry Based Randomized-Controlled Trial of an Upper Limb Exergaming Intervention for Children and Adolescents With Spinal Muscular Atrophy

INFORM SMA
Start date: June 1, 2024
Phase: N/A
Study type: Interventional

We aim to conduct a randomized registry-based waitlist-controlled trial (RCT) with 22 youth with Spinal Muscular Atrophy (SMA) aged 8-18 years to determine if Tales from the Magic Keep is more effective than usual care for improving occupational performance and satisfaction. This clinical trial is embedded in INFORM RARE, an innovative clinical trials network funded by the Canadian Institutes of Health Research (CIHR) Strategy for Patient-Oriented Research (SPOR), co-designed by patients and families, healthcare providers, policymakers, methodologists, and research ethicists (https://www.informrare.ca/). INFORM RARE addresses a recognized need for innovation in treatable pediatric rare diseases to facilitate timely and robust evidence generation in support of knowledge user decision-making. Finally, the study is co-designed by adolescents with SMA and their families, healthcare providers, policymakers, and methodologists, incorporating the SPOR guiding principles of patient engagement at all levels of research.

NCT ID: NCT06363942 Not yet recruiting - Frailty Clinical Trials

A Personalized Video-based Exercise Program for Fall Prevention in Frail and Pre-frail Older Adult

Start date: April 15, 2024
Phase: N/A
Study type: Interventional

This is a randomized interventional clinical trial, whereby 100 participants will be randomized to either follow the SAFE exercise program (experimental group) or not (control group). At the end of the intervention, the experimental group will be encouraged to continue doing the exercises, and the control group will have the opportunity to participate in the SAFE exercises. 12 weeks post-intervention, the investigators will follow up with participants by telephone to follow up whether they are still following the SAFE program or not.

NCT ID: NCT06353945 Not yet recruiting - Vaginal Atrophy Clinical Trials

Perceived Effectiveness of the Vaginal Moisturizer Investigational Product Under Normal Conditions of Use.

Start date: April 29, 2024
Phase: N/A
Study type: Interventional

The present research project aims to evaluate the perceived effectiveness of the product under investigation under normal conditions of use for 28 days, to defend the claims "High hydration power, relief of discomfort and improvement of vaginal tone."

NCT ID: NCT06333782 Not yet recruiting - Vulvar Atrophy Clinical Trials

Evaluation of the Safety and Efficacy of Hyaluronic Acid Injection in Labia Majora Augmentation

Start date: March 31, 2024
Phase: N/A
Study type: Interventional

The goal of this interventional clinical investigation using Genefill Contour® CE marked device outside of its indication is to compare with other hyaluronic acid device already marketed for labia majora augmentation in women with labia majora hypotrophy/atrophy. The primary objective is the evaluation of the safety of Genefill Contour®. The secondary objectives is effectivenes of the investigational device (improvement of patient´s symptoms, patient´s satisfaction, sexual function & pain during injection). Participants will come to a total of 8 visits (including 2 phone calls) over a period of 12 months. Participants would be enrolled in Genefill Contour® or comparator group. An ancillary study would be conducted in a cohort of participants evaluating the increase in volume and distance between labia after HA injection

NCT ID: NCT06321965 Not yet recruiting - Clinical trials for Spinal Muscular Atrophy

Characterization of New Phenotypes of Patients With Spinal Muscular Atrophy Treated With SMN Restoring Therapy

PHENO SMART
Start date: April 1, 2024
Phase: N/A
Study type: Interventional

With the advent of new treatments for ASI, new phenotypes are emerging. The investigators propose to describe these new phenotypes by prospectively following children with ASI of all types treated with TRS and aged under 16 for 2 years. The investigators also propose to evaluate potential assessment tools to determine whether they are relevant for monitoring this population, either routinely or for future clinical trials. The investigators also aim to collect the total costs associated with ASI in order to propose a first prospective medico-economic study in France.

NCT ID: NCT06300996 Not yet recruiting - Clinical trials for Spinal Muscular Atrophy

Spinal Cord Stimulation for the Treatment of Motor Deficits in People With Spinal Muscular Atrophy - Upper Limb

Start date: September 2024
Phase: N/A
Study type: Interventional

Spinal cord stimulation (SCS) has shown remarkable efficacy in restoring motor function in people with spinal cord injury by recruiting afferent input to enhance the responsiveness of spared neural circuits to residual cortical inputs. This pilot will test if SCS can show evidence to improve motor deficits in people with Type 2, 3, or 4 spinal muscular atrophy (SMA). The investigators will enroll up to six subjects with Type 2, 3, or 4 SMA aged 16 or older that show quantifiable motor deficits of the upper body. The investigators will then implant the subjects with percutaneous, linear spinal leads near the cervical spinal cord for a period of up to 29 days. Although these leads are not optimized for motor function but rather for their clinically approved indication of treating pain, the investigators believe they provide a safe technology enabling our team to perform scientific measurement necessary to evaluate potential for effects of SCS in motor paralysis with SMA. After the end of the study, the leads will be explanted.