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Atrophy clinical trials

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NCT ID: NCT05121012 Recruiting - Clinical trials for Multiple System Atrophy

Synaptic Loss in Multiple System Atrophy

Start date: September 1, 2021
Phase:
Study type: Observational

In this study the investigators would like to investigate the degree of damage of the synapses, an important part of the neurons vital for the communications between neurons, in Multiple System Atrophy (MSA).

NCT ID: NCT05118685 Recruiting - Atrophic Vaginitis Clinical Trials

Estrogen and Platelet Rich Plasma in Treatment of Atrophic Vaginitis

Start date: November 13, 2021
Phase: Phase 1
Study type: Interventional

This study is designed to compare the efficacy, acceptability, and safety of vaginal estrogen cream and platelet-rich plasma in pt. complaining of atrophic vaginitis.

NCT ID: NCT05115110 Recruiting - Clinical trials for Spinal Muscular Atrophy (SMA)

A Study to Investigate the Safety and Efficacy of RO7204239 in Combination With Risdiplam (RO7034067) in Participants With Spinal Muscular Atrophy

MANATEE
Start date: June 2, 2022
Phase: Phase 2/Phase 3
Study type: Interventional

Risdiplam works by helping the body produce more survival motor neuron (SMN) protein throughout the body. This means fewer motor neurons - nerve cells that pass impulses from nerves to muscles to cause movement - are lost, which may improve how well muscles work in people with SMA. RO7204239 is an investigational anti-myostatin antibody that is designed to target myostatin. Myostatin plays an important role in the regulation of skeletal muscle size by controlling growth. Inhibiting myostatin may help muscles grow in size and strength. RO7204239 in combination with risdiplam, which is designed to increase the amount of SMN protein throughout the body, has the potential to further improve motor function and clinical outcomes for people living with SMA. This trial will study the safety and efficacy of RO7204239 in combination with risdiplam in patients with spinal muscular atrophy (SMA). The trial has two parts; Part 1 is the dose-finding part in SMA patients that are either ambulant (aged 2-10 years) or non-ambulant (aged 5-10 years) within separate cohorts, and Part 2 is the pivotal part in SMA patients aged 2-25 years that are ambulant.

NCT ID: NCT05110885 Not yet recruiting - Clinical trials for Duchenne Muscular Dystrophy

Public AttitudesTowards SMA and DMD Awareness, Newborn and Carrier Screening and Physiotherapy Practices

Start date: November 2021
Phase:
Study type: Observational

The addition of SMA and DMD muscle diseases to newborn screening and premarital carrier screening has been controversial. In this study, researchers aim to measure the awareness level of SMA and DMD muscle diseases of individuals living in Turkey and to obtain information about their attitudes towards newborn and carrier screening and physiotherapy practices. Thus, this study aimed to determine the factors that affect people's views on this subject.

NCT ID: NCT05109637 Completed - Clinical trials for Spinal Muscular Atrophy

A Study to Assess the Clinical Validity of Konectomâ„¢ in Adults Living With Neuromuscular Disorders

DigiNOA
Start date: February 10, 2022
Phase: N/A
Study type: Interventional

The primary objective of the study is to explore the convergent validity of smartphone-based Konectom DOAs against in-clinic standard assessments. The secondary objectives of this study are to evaluate the test-retest reliability of smartphone-based Konectom Digital Outcome Assessments (DOAs); to determine the relationship between Konectom upper limb DOAs and conventional upper limb assessments in clinical environments; to determine the relationship between Konectom lower limb DOAs and status of ambulation in clinical environments; to evaluate group differences in smartphone-based Konectom DOAs [self-administered at home and in-clinic] between person with spinal muscular atrophy (PwSMA) and healthy subjects (HS); to evaluate the variability of Konectom DOAs self-administered in everyday environment in HS and PwSMA; to compare Konectom DOAs between in-clinic supervised administration versus self-assessments in everyday environment in HS, PwSMA groups; to evaluate the relationship of Konectom DOAs against patient-reported outcomes (PROs) in PwSMA and to evaluate the clinical safety of Konectom in PwSMA.

NCT ID: NCT05109091 Active, not recruiting - Clinical trials for Multiple System Atrophy

Study of ATH434 in Participants With Multiple System Atrophy

Start date: July 1, 2022
Phase: Phase 2
Study type: Interventional

This study will assess the safety and efficacy of ATH434 in participants with Multiple System Atrophy

NCT ID: NCT05108324 Not yet recruiting - Clinical trials for Edentulous; Alveolar Process, Atrophy

Reliability of All on 4 Using 2 Zygomatic and 2 Conventional Implants vs All on 4 Implants for Rehabilitation of Maxilla

Start date: November 10, 2021
Phase: N/A
Study type: Interventional

Oral rehabilitation by dental implants in the severely atrophic maxilla often represents a challenge. To overcome this difficulty, bone augmentation procedures such as sinus augmentation, guided bone regeneration (GBR), or distraction osteogenesis have been used to obtain adequate bone height and width for proper three-dimensional implant placement. To avoid surgical morbidity and shorten treatment length, alternative methods such as short or tilted implants, as well as zygomatic implants (ZIs),have been proposed and have shown promising outcomes.

NCT ID: NCT05104476 Active, not recruiting - Clinical trials for Multiple System Atrophy

A Study of Lu AF82422 in Participants With Multiple System Atrophy

AMULET
Start date: November 16, 2021
Phase: Phase 2
Study type: Interventional

To find out the effect of Lu AF82422 on disease progression in participants with multiple system atrophy.

NCT ID: NCT05097092 Recruiting - Clinical trials for Muscle Disuse Atrophy

Strength Training Augmenting Rehabilitation

STAR
Start date: August 13, 2021
Phase: N/A
Study type: Interventional

This project aims to determine whether a novel strength training rehabilitation protocol can diminish the negative consequences of limb immobilization and expedite the restoration of muscle function during retraining in healthy individuals.

NCT ID: NCT05095597 Recruiting - Asherman Syndrome Clinical Trials

Umbilical Cord Plasma for Treating Endometrial Pathologies (Thin Endometrium / Asherman's Syndrome/ Endometria Atrophy)

hSCU-PRP
Start date: April 22, 2022
Phase: Phase 2
Study type: Interventional

In the last years, platelet-rich plasma (PRP) has emerged as a promising alternative to treat endometrial pathologies affecting the endometrial lining. Different studies have tried this therapeutic approach in human patient, but results are not conclusive at all. Also, in the last years, different studies have suggested the umbilical cord blood has a stronger reservoir of growth factors and other pro-regenerative molecules than the adult peripheral blood. That is the reason why the present study aims to evaluate if using platelet-rich plasma obtained from umbilical cord blood is able to increase endometrial thickness and prepare the endometrium for an embryo transference. However, due to the novelty of this approach, the investigators have considered to include a 'proof of concept' group (women with premature ovarian insufficiency) to obtain a deeper understanding of the clinical value of this blood derivative.