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NCT ID: NCT06150716 Recruiting - Clinical trials for Pelizaeus-Merzbacher Disease

Orbit Study: A Study to Evaluate the Safety, Pharmacokinetics, and Pharmacodynamics of Intrathecally Administered ION356 in Participants With Pelizaeus Merzbacher Disease (PMD)

Start date: April 10, 2024
Phase: Phase 1
Study type: Interventional

The primary purpose of this study is to evaluate the safety and tolerability of ION356.

NCT ID: NCT06150664 Recruiting - Clinical trials for Non Small Cell Lung Cancer

A Phase 1 of CTX-8371 in Patients With Advanced Malignancies

Start date: March 19, 2024
Phase: Phase 1
Study type: Interventional

This is a Phase 1, open-label, first-in-human study of CTX-8371 administered as a monotherapy in patients with metastatic or locally advanced malignancies. The study will be conducted in 2 cohorts: Dose Escalation and Dose Expansion.

NCT ID: NCT06150612 Not yet recruiting - Migraine Clinical Trials

Unwinding Anxiety for Migraine: Pilot

UAM
Start date: January 3, 2024
Phase: N/A
Study type: Interventional

This is a pilot study that aims to understand the feasibility and acceptability of a mobile health educational app plus group-based mindfulness therapy on anxiety and migraine-related disability among people with migraine.

NCT ID: NCT06150599 Not yet recruiting - Clinical trials for Chronic Pelvic Pain Syndrome

Sacral Neuromodulation for Chronic Pelvic Pain

SNM_CPP
Start date: July 2024
Phase: N/A
Study type: Interventional

Sacral neuromodulation (SNM) is a safe, effective, and minimally invasive FDA approved treatment for urinary and fecal incontinence, urinary frequency, urgency, and urinary retention. In this study we are assessing the effectiveness of sacral neuromodulation in women with suffering from chronic pelvic pain (CPP), through a single device implant procedure.

NCT ID: NCT06150573 Active, not recruiting - Dentin Sensitivity Clinical Trials

A Study Assessing the Effects of an Experimental Dentifrice in Maintaining Tooth Color Following Tooth Bleaching

Start date: November 27, 2023
Phase: N/A
Study type: Interventional

The main aim of this study is to investigate the ability of an experimental dentifrice containing 5 percent (%) potassium nitrate (KNO3), 1% alumina and 5% sodium tripolyphosphate (STP), to maintain tooth color and reduce extrinsic dental stain accumulation following peroxide tooth bleaching compared to a regular fluoride dentifrice.

NCT ID: NCT06150560 Recruiting - High Blood Pressure Clinical Trials

A Study of Angiotensin-II Receptor Blocker on Cardiovascular Remodeling (VALUE Trial)

VALUE
Start date: April 1, 2024
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the effectiveness and mechanism of action of Losartan in the treatment of coarctation of aorta.

NCT ID: NCT06150547 Enrolling by invitation - CNS Malignancy Clinical Trials

A Study of Metabolic Agents Following Brain Radiation

Start date: November 14, 2023
Phase:
Study type: Observational

This research is being done to determine if CEST Magnetic Resonance Imaging and F-dopa PET are feasible techniques to detect metabolic differences between tumor and brain.

NCT ID: NCT06150534 Recruiting - Clinical trials for Primary Immunodeficiency Diseases (PID)

At-Home Subcutaneous Immunoglobulin Replacement Therapy Using Alexa Skill

Start date: December 27, 2023
Phase:
Study type: Observational

The main aim of this study is to determine the impact of digital health technology, such as Alexa Skill, used to support the initiation of home-based subcutaneous immunoglobulin (SCIG) treatment, treatment management, and overall participant experience.

NCT ID: NCT06150443 Recruiting - Clinical trials for Carpal Tunnel Syndrome

Pilot Study Evaluating the Elasticity and Shear Wave Modulus (Stiffness) of the Median Nerve in Patients With Mild to Moderate Idiopathic Carpal Tunnel Syndrome Receiving OMT and Conservative Therapy

COMET-AOA
Start date: February 26, 2024
Phase: N/A
Study type: Interventional

To evaluate and quantify changes in the elasticity and shear wave modulus (stiffness) of the median nerve in patients diagnosed with mild to moderate carpal tunnel syndrome following osteopathic manipulative therapy.

NCT ID: NCT06150417 Recruiting - Prostate Cancer Clinical Trials

MDRT in Prostate Cancer Treated With Long-term Androgen Deprivation Therapy in the STAMPEDE Trial (METANOVA)

Start date: May 24, 2024
Phase: Phase 2
Study type: Interventional

The purpose of this study is to find out if giving radiation therapy (RT) to areas of metastatic prostate cancer at the time a participant is diagnosed will help control disease better than the usual treatment. This treatment is called metastasis-directed radiotherapy (MDRT). The usual treatment for prostate cancer that has spread to other parts of the body is to give lifelong treatment with hormone therapy (also known as androgen deprivation therapy or ADT). Participants may also be given prostate RT even if the disease is metastatic. Participants will receive hormone therapy (the standard treatment for prostate cancer) for 12 months. The hormone therapy agents may be taken by mouth or given as an injection. Participants will also have prostate RT. Up to 50 participants will have surgery to remove the prostate instead of having prostate RT. A portion of the participants will be randomized to receive MDRT to areas where the cancer has spread. For participants who have surgery to remove their prostate, they will be asked to allow tissue samples collected during the surgery to be sent to an outside lab for research tests and extra blood samples drawn for research tests before starting the study, and at the time the cancer becomes worse if applicable. Participation in the study will last approximately 12 months, and will be followed by their doctor for up to five years per standard of care. The main goal is to compare the efficacy of the standard of care (standard systemic therapy + definitive prostate-directed local therapy) versus the standard of care with metastasis-directed radiotherapy (MDRT) for consolidation of metastatic disease.