Vosoritide for Short Stature in Turner Syndrome
NCT05849389
Recruiting
Turner syndrome (TS) is characterized by a missing whole or part of the second sex chromosome in a phenotypic female, resulting in short stature due to haploinsufficiency of the short-stature homeobox-containing (SHOX) gene. Growth hormone (GH) is an approved therapy for this condition, although not associated with GH deficiency, and benefits are modest. Vosoritide, a C-type natriuretic peptide (CNP) analog, targets chondrocytes within the growth plate leading to increased cell proliferation and... Read More
Gender:
FEMALE
Ages:
Between 3 years and 11 years
Trial Updated:
06/20/2024
Locations: Children's National Hospital, Washington, District of Columbia
Conditions: Turner Syndrome, Short Stature
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Detection of EEG-Based Biomarkers of Chronic Low Back Pain
NCT06025201
Recruiting
Chronic low back pain (CLBP) is a pervasive disorder affecting up to one-fifth of adults globally and is the single greatest cause of disability worldwide. Despite the high prevalence and detrimental impact of CLBP, its treatments and mechanisms remain largely unclear. Biomarkers that predict symptom progression in CLBP support precision-based treatments and ultimately aid in reducing suffering. Longitudinal brain-based resting-state neuroimaging of patients with CLBP has revealed neural network... Read More
Gender:
ALL
Ages:
Between 18 years and 80 years
Trial Updated:
06/20/2024
Locations: Stanford's Systems and Neuroscience Pain Lab, Palo Alto, California
Conditions: Chronic Low-back Pain, Healthy
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Application of a Systematic Developmental Assessment to a Novel Population: Infants With Rare Genetic Disorders
NCT03967743
Recruiting
The main objective of this study is to apply a well-established model of developmental surveillance (which evolved to characterize the outcomes of very low birth weight infants) to infants with genetic disorders. A novel clinical model for infants with rare genetic disorders has been created as a joint initiative between the Division of Newborn Medicine's NICU Growth and Developmental Support Programs (NICU GraDS) program and the Division of Genetics at Boston Children's Hospital (BCH). This stu... Read More
Gender:
ALL
Ages:
4 years and below
Trial Updated:
06/19/2024
Locations: Boston Children's Hospital, Boston, Massachusetts
Conditions: Genetic Disease, Genetic Syndrome, Genetic Predisposition to Disease, Development, Infant, Development, Child
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Metformin and Nightly Fasting in Women With Early Breast Cancer
NCT05023967
Recruiting
This phase IIb trial studies the combined effect of prolonged nightly fasting and metformin hydrochloride extended release in decreasing breast tumor cell proliferation and other biomarkers of breast cancer. Preventing invasive breast cancer or DCIS. Metformin is widely used to treat type II diabetes and is associated with a decreased risk of cancer and death in diabetic individuals. Intermittent fasting may protect cancer patients from the toxic effects of chemotherapy agents without causing ch... Read More
Gender:
FEMALE
Ages:
18 years and above
Trial Updated:
06/19/2024
Locations: M D Anderson Cancer Center, Houston, Texas +2 locations
Conditions: Anatomic Stage I Breast Cancer AJCC v8, Anatomic Stage II Breast Cancer AJCC v8, Breast Ductal Carcinoma In Situ, Invasive Breast Carcinoma
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pBI-11 & TA-HPV (With Pembrolizumab as Treatment for Patients w/Advanced, PD-L1 CPS≥1, hrHPV+ Oropharyngeal Cancer
NCT05799144
Recruiting
This phase II trial tests how well pB1-11 and human papillomavirus tumor antigen (TA-HPV) vaccines in combination with pembrolizumab work in treating patients with oropharyngeal cancer that has come back (recurrent) or that has spread from where it first started (primary site) to other places in the body (metastatic) and that is PD-L1 and human papillomavirus (HPV) positive. Oropharyngeal cancer is a type of head and neck cancer involving structures in the back of the throat (the oropharynx), su... Read More
Gender:
ALL
Ages:
18 years and above
Trial Updated:
06/19/2024
Locations: Vanderbilt University/Ingram Cancer Center, Nashville, Tennessee
Conditions: Metastatic Oropharyngeal Carcinoma, Recurrent Oropharyngeal Carcinoma
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More Sleep: Pain Response to Longer Sleep
NCT05816434
Recruiting
This study is being done to find out whether extending sleep for at least an hour per night, seven days a week, predicts a higher tolerance and a higher threshold for pain. This is a 21-day study. Participants will be asked to wear sleep- and heart- monitoring watches. Pressure pain and cold pain will be measured at study visits.
Gender:
ALL
Ages:
Between 18 years and 24 years
Trial Updated:
06/19/2024
Locations: Pennsylvania State University, University Park, Pennsylvania
Conditions: Sleep, Pain
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Phase 3 Study of Toripalimab Alone or in Combination With Tifcemalimab as Consolidation Therapy in Patients With Limited-stage Small Cell Lung Cancer (LS-SCLC)
NCT06095583
Recruiting
The Study is a Phase 3, randomized, three-arm, double-blind, placebo-controlled, multi-regional clinical research study to evaluate the safety and efficacy use of toripalimab alone or in combination with tifcemalimab as consolidation therapy in patients with limited-stage small cell lung cancer without disease progression following chemoradiotherapy. Tifcemalimab is a monoclonal antibody against B and T lymphocyte attenuator (BTLA). Toripalimab is a monoclonal antibody against programmed death... Read More
Gender:
ALL
Ages:
18 years and above
Trial Updated:
06/19/2024
Locations: Banner MD Anderson Cancer Center, Goodyear, Arizona +155 locations
Conditions: Limited-stage Small Cell Lung Cancer (LS-SCLC)
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mHealth + e-Navigator Stepped Care on ART Adherence in Latino MSM
NCT06375135
Recruiting
The goal of this study is to evaluate the efficacy of stepped care strategies to improve ART adherence among adult Latino MSM with HIV using a sequential, multiple assignment, randomized trial (SMART). The trial will compare a stepped care strategy of delivering TXTXT ("Treatment Text") first and stepping up to remote patient navigation for non-responders vs. a stepped care strategy of delivering TXTXT + e-Navigation first and stepping up to EMA-supported e-Navigation for non-responders. Both TX... Read More
Gender:
MALE
Ages:
18 years and above
Trial Updated:
06/19/2024
Locations: Care Resource Community Health Centers, Inc., d/b/a CARE RESOURCE, Miami, Florida
Conditions: ART Adherence
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Evaluation of a Monofocal Intraocular Lens
NCT06428955
Recruiting
The aim of this study is to investigate the 3-month visual performance of the CT LUCIA 621P IOL, a hydrophobic aspheric monofocal IOL with a non-constant aspheric optic profile in adult patients 50 years of age or older who are undergoing cataract surgery.
Gender:
ALL
Ages:
50 years and above
Trial Updated:
06/19/2024
Locations: Price Vision Group, Indianapolis, Indiana +3 locations
Conditions: Cataract
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Early Intervention for Information Processing Speed Deficits in Acute SCI: A Pilot Study
NCT06452264
Recruiting
This study seeks to conduct a pilot study to test whether a cognitive training program can improve processing speed abilities in individuals with acute traumatic spinal cord injury.
Gender:
ALL
Ages:
Between 18 years and 65 years
Trial Updated:
06/19/2024
Locations: Kessler Foundation, East Hanover, New Jersey
Conditions: Spinal Cord Injuries, Cognitive Dysfunction, Cognitive Impairment, Acute Spinal Cord Injury
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Virtual Reality During Exercise Testing
NCT06464406
Recruiting
The goal of this clinical trial is to explore the effects of virtual reality use on maximal aerobic exercise test performance (aerobic capacity) in healthy adults. The main questions it aims to answer are: * Does using a virtual reality program during a maximal aerobic exercise test lead to differences in VO2peak (maximal aerobic capacity)? and, * Does using a virtual reality program during a maximal aerobic exercise test lead to differences in work rate at the ventilatory threshold? Participa... Read More
Gender:
ALL
Ages:
18 years and above
Trial Updated:
06/19/2024
Locations: Augusta University, Augusta, Georgia
Conditions: Virtual Reality
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Assessing the Functional Movement Screen as a Reliable Physical Therapy Discharge Criteria for Chronic Lower Back Pain Patients
NCT06474429
Recruiting
Overview of Research Design and Objectives This study is a prospective, concurrent cohort study aimed at evaluating the reliability of the Functional Movement Screen (FMS) as a discharge criterion for patients with chronic lower back pain (LBP) undergoing physical therapy. The primary objective is to identify a benchmark FMS score that correlates with a low risk of recurrence and high levels of functional performance post-discharge. Specific Aims and Hypotheses The study specifically aims to:... Read More
Gender:
ALL
Ages:
Between 18 years and 49 years
Trial Updated:
06/19/2024
Locations: Texas Back Institute, Plano, Texas
Conditions: Chronic Lower Back Pain
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