Clin2
NCT07332013Possibly a fitRecruiting

Urine titin test for Duchenne muscular dystrophy

Duchenne Muscular Dystrophy (DMD)Becker's Muscular Dystrophy (BMD)

Part of Bones, joints & muscles, Brain & nervous system, Genetic & congenital clinical trials.

This study measures a protein called titin in urine to see if it can help track muscle damage in boys with Duchenne or Becker muscular dystrophy. It also includes healthy boys for comparison.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
50 people
Ages
2 years to 10 years
Study type
Interventional

Who can take part

  • You are a boy or young man
  • You have a confirmed diagnosis of Duchenne or Becker muscular dystrophy (or you are a healthy child without these conditions)
  • You can walk on your own without help
  • Your home has electricity and a freezer to store urine samples

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

Similar studies

Other trials that look related to this one.

NCT07664124Not yet recruiting
Tracking arm use at home in non-walking boys with Duchenne

This study uses a small wearable device (called Syde) to track arm and hand movement in boys with Duchenne who can no longer walk. The goal is to see if this device can help doctors understand how arm function changes over time, which may guide future care.

Liège
NCT07423026Recruiting
Remote study using technology to track DMD in young boys

This study uses remote technology, like apps or wearable devices, to monitor motor skills and development in boys with Duchenne muscular dystrophy (DMD). It aims to find better ways to measure how the disease progresses over time without requiring frequent clinic visits.

Oxford
NCT06839469Recruiting
Walking study for rare muscle and nerve conditions

This study looks at how children and teens with Duchenne muscular dystrophy (DMD) or spinal muscular atrophy (SMA) walk, by having them do walking tests while wearing sensors. The goal is to find better ways to track how these diseases progress and how treatments work over time, without needing blood tests or scans.

Palo Alto, California
NCT07092540Recruiting
Baby Duchenne Study: Early Years in Boys With DMD

This study tracks development and health in young boys with Duchenne muscular dystrophy during the first three years of life. It aims to better understand early signs and how the condition progresses, which may help improve care and future treatments.

Rochester, New York
NCT07608432Recruiting· Phase 3
Testing a New DMD Treatment Given Every 4 Weeks

This study tests whether a new medicine called zeleciment rostudirsen can help ambulatory (walking) males with Duchenne muscular dystrophy (DMD). The medicine is given as an intravenous infusion (through a vein) every 4 weeks and works by helping the body produce a protective muscle protein.

Hillsborough, North Carolina
NCT06643923Not yet recruiting
Pelvic and lower back exercises for Duchenne muscular dystrophy

This study tests a physiotherapy program focused on the lower back and pelvis for children with Duchenne muscular dystrophy who can still walk. It may help improve bladder control and overall function.

Ankara, Çankaya

Hear when a new Duchenne Muscular Dystrophy (DMD) trial opens

We’ll email you when one opens — at most once a week, no account needed, unsubscribe anytime.