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NCT ID: NCT06268704 Recruiting - Clinical trials for Sacroiliac Joint Dysfunction

Particulate vs. Non-Particulate Steroid for Sacroiliac Joint Injection

Start date: March 27, 2024
Phase: Phase 4
Study type: Interventional

This study will compare two different corticosteroids (dexamethasone and methylprednisolone) for use in sacroiliac joint injections to treat SI joint pain.

NCT ID: NCT06268522 Recruiting - Low Back Pain Clinical Trials

Adjunctive Mindfulness During Opioid Tapering for patientS With Chronic Pain (The AMOS Study)

Start date: February 2024
Phase: N/A
Study type: Interventional

This study is a Randomized Controlled Trial exploring the effects of a Mindfulness interventions in reducing pain interference and opioid dose in patients with Chronic Low Back Pain. A total of 200 opioid-using patients with chronic pain, male and female participants will be enrolled, with a need for 160 completers. Patient will be randomly assigned into the Mindfulness-Oriented Recovery Enhancement or the Psychoeducation comparison control group.

NCT ID: NCT06268431 Recruiting - Prolonged Labor Clinical Trials

Oxytocin Rest to Reduce Cesarean Delivery

ORCA
Start date: February 15, 2024
Phase: N/A
Study type: Interventional

Prolonged labor is usually managed with continuous oxytocin infusion. "Oxytocin rest" has been proposed as a strategy to resolve protracted labor in patients who have received continuous oxytocin without progress. This strategy involves discontinuing oxytocin then restarting infusion after a period of time, under the theory that washout of the oxytocin receptor will strengthen uterine contractions to improve labor progress. "Oxytocin rest" is performed on labor and delivery units across the United States. Yet, there is no randomized or prospective data to support the practice. The purpose of this study is to assess whether oxytocin rest of 60 minutes in patients with prolonged labor reduces risk for cesarean delivery.

NCT ID: NCT06268288 Recruiting - Clinical trials for Autonomic Dysfunction

Non-invasive Vagal Neurostimulation (nVNS) in Adolescents With Postural Orthostatic Tachycardia Syndrome (POTS)

Start date: February 14, 2024
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if nVNS will decrease autonomic symptom intensity (COMPASS-31 and Child Functional Disability Inventory) in adolescent patients with postural orthostatic tachycardia syndrome (POTS) in comparison to standard recovery STEPS management.

NCT ID: NCT06268197 Recruiting - Chronic Pain Clinical Trials

Interoception-Based Yoga for Chronic Pain

Start date: February 16, 2024
Phase: N/A
Study type: Interventional

The purpose of this research is to examine the feasibility and acceptability of an interoception-based yoga program for chronic pain. Interoception involves your ability to feel sensations in your body (such as your heartbeat or muscle tension) as well as how you think about and interpret those sensations. Interoception may be an important component of chronic pain and the research team is studying whether yoga can change how you feel, think about, and interpret sensations in your body.

NCT ID: NCT06268145 Recruiting - Clinical trials for Type 2 Diabetes Mellitus

ECC5004 RBA FE Study in Healthy Participants

Start date: February 6, 2024
Phase: Phase 1
Study type: Interventional

This study is a Phase 1, open-label, randomized, single dose, fixed sequence, crossover study designed to compare the relative bioavailability of 50 mg ECC5004 current tablet formulation (F1) and 50 mg ECC5004 new tablet formulation (F2) under fasted and fed conditions in healthy participants

NCT ID: NCT06268041 Recruiting - Stroke Clinical Trials

HIT-Stroke Trial 2

HST2
Start date: February 9, 2024
Phase: N/A
Study type: Interventional

People who had a stroke at least 6 months prior and who still have difficulty with walking will each be randomly assigned to receive either moderate or vigorous intensity walking exercise. Both protocols will be performed individually with a physical therapist for 45 minutes, 3x/week for 12 weeks. Measures including walking function will be assessed at baseline (PRE), after 4, 8 and 12 weeks of training (12WK) and at 3-month follow up (3moPOST), by raters who are unaware of the participant randomization.

NCT ID: NCT06267846 Recruiting - Clinical trials for Major Depressive Disorder

A Study to Evaluate the Efficacy and Safety of NBI-1070770 in Adults With Major Depressive Disorder

Start date: March 20, 2024
Phase: Phase 2
Study type: Interventional

To evaluate the efficacy, safety, and tolerability of NBI-1070770 compared to placebo on improving symptoms of depression in participants with major depressive disorder (MDD).

NCT ID: NCT06267729 Recruiting - Clinical trials for Metastatic Prostate Cancer

Study of AZD0754 in Participants With Metastatic Prostate Cancer

APOLLO
Start date: March 12, 2024
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety, tolerability, and antitumour activity of AZD0754 CAR T-cell therapy in participants with metastatic prostate cancer.

NCT ID: NCT06267547 Recruiting - Physical Activity Clinical Trials

Healthy Activities Improve Lives (HAIL)

HAIL
Start date: April 23, 2024
Phase: N/A
Study type: Interventional

The investigators have developed an online platform to support the 8-week, F&S! exercise program called the Healthy Activity Improves Lives (HAIL) online platform. The aim of this study is to perform a cluster randomization of four racially diverse churches or senior centers to either the standard F&S! program, or the combined HAIL Online Platform + F&S! program to examine the efficacy of the HAIL online platform + F&S! program for older adults in black communities.