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Found 296 clinical trials
Cystic Fibrosis - Insulin Deficiency Early Action

Cystic Fibrosis (CF) is the most common life-threatening genetic condition affecting Australian children. As well as repeated lung infections, children with CF develop insulin deficiency and

antibiotics
malnutrition
insulin
genetic disorder
oral glucose tolerance test
  • 57 views
  • 27 Sep, 2021
  • 6 locations
Theophylline Treatment for Pseudohypoparathyroidism - Children 2-12 Years Old

Pseudohypoparathyroidism is a genetic disorder with limited treatment options, characterized by early-onset obesity, short stature and resistance to multiple hormones. This phase 2 clinical

  • 0 views
  • 07 Oct, 2021
  • 1 location
Improving Therapeutic Adherence With a Co-constructed Program Involving Both Patients and Health Care Professionals

Background Cystic fibrosis is a life-threatening genetic disorder responsible for pulmonary failure and multi-systemic complications involving specific and large medical care burden. To date, no

fibrosis
genetic disorder
  • 0 views
  • 09 Apr, 2022
Core Stability Exercises and Hereditary Ataxia (Core-ataxia)

The hereditary ataxias are a group of genetic disorders characterized by slowly progressive incoordination of gait and balance impairments in sitting and standing. Trunk local stability during

  • 0 views
  • 23 May, 2022
Hereditary Risk Factors for Thyroid Cancer

Thyroid cancers can occur sporadically, but can also be found as tumors that cluster in families with other cancers or genetic syndromes. Researchers are studying thyroid cancer in children and

cancer
thyroid nodule
Accepts healthy volunteers
  • 10 views
  • 16 May, 2022
  • 1 location
PINPOINT: Gaming Technology for SCD Pain (Pinpoint II)

Sickle cell disease (SCD) is a common genetic disorder characterized by episodes of pain, yet programs to assist SCD adolescents with better identification and communication about pain are

genetic disorder
Accepts healthy volunteers
  • 0 views
  • 26 Jan, 2022
  • 2 locations
Realization of Sequencing of All Known Human Genes in Case of Detection of Cerebral Renal or Ophthalmological Fetal Malformations During Pregnancy in Order to Make an Etiological Diagnosis and to Precise the Fetal Prognosis

features as part of a syndromic condition. For some malformations strongly suggestive of a genetic condition, we propose to realize an exome (i.e. all coding parts of the genome) sequencing of the

  • 0 views
  • 26 Jan, 2021
  • 12 locations
A Study of CAP-1002 in Ambulatory and Non-Ambulatory Patients With Duchenne Muscular Dystrophy (HOPE-3) (HOPE-3)

HOPE-3 is a multi-center, randomized, double-blind, placebo-controlled clinical trial evaluating the safety and efficacy of a cell therapy called CAP-1002 in study participants with Duchenne muscular dystrophy (DMD) and impaired skeletal muscle function. Non-ambulatory and ambulatory boys and young men who meet eligibility criteria will be randomly assigned to receive …

duchenne muscular dystrophy
cell therapy
glucocorticoids
respiratory assessment
  • 0 views
  • 05 Jun, 2022
  • 2 locations
Improving Care of Prader-Willi Syndrome : Evaluation of a New Care Program Combining Adapted Physical Activity, Nutrition and Therapeutic Education (APHYNET)

Prader-Willi syndrome (PWS) is a rare and complex genetic disease characterized by hypothalamic-pituitary axis dysfunction combining eating disorders associated with hyperphagia and satiety

  • 0 views
  • 14 Mar, 2022
  • 1 location
Gene Transfer for X-Linked Severe Combined Immunodeficiency in Newly Diagnosed Infants (LVXSCID-ND)

SCID-X1 is a genetic disorder of blood cells caused by DNA changes in a gene that is required for the normal development of the human immune system. The purpose of this study is to determine if

  • 26 views
  • 25 Mar, 2022
  • 3 locations