Clinical trials

232

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Person-Centered Quality Measurement and Management in a System for Addictions Treatment in New York State (Project 3)

The goal of this study is to implement Opioid Use Disorder Quality Measurement and Management (OUD-QM2) strategy by the Office of Addiction Services and Supports (OASAS) to drive change and improve treatment practices. Through a concurrent mixed methods approach that iteratively examines quantitative and qualitative data to inform the process, the investigators will examine the effects of the strategy on stakeholders-PWUD/patients, families, and providers-and outcomes. This comprehensive approach will allow for a "global" view of the perceived effects of the OUD-QM2 strategy for all stakeholders while allowing us to use administrative data to test the effects of the strategy on patient outcomes. Through qualitative interviews and focus groups conducted in years 1, 3, and 5 of the phase, the investigators will derive information from stakeholders about their perceptions and use of the quality measures. Through surveys conducted with all clinics, the investigators will elicit data on changes in provider use of quality measures, clinical practice, and use of measures for incentive-based contracting. Finally, the investigators will conduct a stepped wedge trial to examine the effects of performance coaching that guides clinics on use of the quality measures for clinical practice improvement. The trial will also benefit from a treatment as usual (TAU) condition of clinics not participating in the trial to examine secular trends in patient outcomes across the period of the OASAS QM2 strategy rollout. The overall aim is to build and test a science-based OUD-QM2 strategy for person-centered treatment.

Participants needed: 35
Trial details
Age: 18-64Biological sex: AllType: InterventionalSponsor: NYU Langone HealthUpdated: Jul 13, 2026Locations: 1
Eligibility criteria

Individuals 18 years of age, and older [+1]

There are no exclusion criteria related to sex/gender to increase the generaliza...

Status: Not yet recruiting

High-protein plUs reSistance Training in gLucagon-like pEptide 1 Receptor Agonist Users (HUSTLE)

The primary objective of this study is to examine the effects of a high-protein diet (HP) paired with resistance training (RT) compared with a HP diet alone, on skeletal muscle mass (SMM) volume of the (a) quadriceps and (b) rhomboids, and upper and lower body muscle strength in adults recently prescribed tirzepatide. The secondary objectives of this study are to compare changes in resting energy expenditure (REE), adaptive thermogenesis (AT), and body adiposity (SFV, VAT, and intramuscular FF) in the quadriceps and rhomboid muscles) between the high-protein diet with RT and the high-protein diet arms at 6 months.

Participants needed: 32
Trial details
Age: 30-60Biological sex: AllType: InterventionalSponsor: NYU Langone HealthUpdated: Jul 13, 2026Locations: 1
Eligibility criteria

Age 30- 60 years [+11]

Patients currently prescribed oral or injectable incretin mimetics containing GL... [+28]

Status: Not yet recruiting

Noise Reduction With Hearing Aids

The purpose of this study is to use an optimized version of the SEDA algorithm (SEDA-HA) for hearing aids to evaluate the benefit for listeners with varying degrees of hearing loss in realistic environments and evaluate its impact on speech perception and sound quality. The primary objective is to evaluate performance with and without the SEDA-HA algorithm on speech perception and speech reception tasks. The secondary objective is to evaluate performance of and experience with SEDA-HA integrated into a portable hearing aid prototype in the laboratory and in real-world situations outside the laboratory.

Participants needed: 60
Trial details
Age: 16+Biological sex: AllType: InterventionalSponsor: NYU Langone HealthUpdated: Jul 13, 2026Locations: 1
Eligibility criteria

16 years of age and older [+3]

under 16 years of age [+1]

Status: Recruiting

Implementation of Communication Disability Collection and Accommodations in Primary Care Settings

This multi-methods-multi-site study aims to adapt and evaluate the effects of an implementation support package of strategies to assist primary care clinics in documenting patients' communication disability (CD) and accommodation needs in the electronic health record (EHR) and providing communication accommodations through EHR data extraction, surveys, focus groups, interviews, and clinical practice observations.

Participants needed: 126,870
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: NYU Langone HealthUpdated: Jul 2, 2026Locations: 5
Eligibility criteria

Adults 18+ years [+6]

Patients whose records are unavailable due to technical issues. [+10]

Status: Not yet recruiting

Sexual Health Communication Skills Training Intervention for Patients With Prostate Cancer

This is a pilot randomized controlled trial of a sexual health communication skills training multimedia intervention (Starting the Conversation \[STC\] adapted for patients with prostate cancer \[PCa\]) to improve patients' ability to communicate with providers about their sexual health concerns during PCa care compared to a time and attention control arm.

Participants needed: 100
Trial details
Age: 18+Biological sex: MaleType: InterventionalSponsor: NYU Langone HealthUpdated: Jul 1, 2026Locations: 1
Eligibility criteria

Adult male with PCa at least 18 years of age [+6]

Individual with impaired decision-making capacity. [+1]

Status: Recruiting

Early Cochlear Implant Use

This observational study will examine newly activated cochlear implant users and determine whether their abilities to discern simple sounds change and relate to improved speech perception. Take-home computers and test-equipment will be sent home, and subjects will complete approximately 25 test sessions over the first 3 months of cochlea implant use. Then, subjects will be tested 3 more times in the laboratory until 1 year-post activation. The primary objective is to determine and quantify how sounds change and speech perception improves over the course of early cochlear implant use.

Participants needed: 25
Trial details
Age: 18-85Biological sex: AllType: ObservationalSponsor: NYU Langone HealthUpdated: Jul 1, 2026Locations: 1
Eligibility criteria

Postlingually deaf cochlear implant users [+4]

Diagnosed cognitive or communicative disorders (other than deafness) [+2]

Status: Recruiting

Feasibility of Home-Based Intermittent 60Hz Light Therapy for Major Depressive Disorder (MDD)

This pilot study evaluates the feasibility, safety, and preliminary efficacy of home-based 60Hz intermittent light therapy in adults with a major depressive episode (MDE). Participants will be randomized in a 2:1 ratio to receive either active or sham 60Hz intermittent light stimulation for 30 minutes daily (Monday through Friday) over three weeks. The light is delivered through a wearable headset. Clinical assessments will be conducted remotely at baseline, mid-point, post-treatment, and follow-up to measure changes in depressive symptoms.

Participants needed: 40
Trial details
Age: 24-65Biological sex: AllType: InterventionalSponsor: NYU Langone HealthUpdated: Jun 29, 2026Locations: 1
Eligibility criteria

Age between 24 and 65 years (inclusive)*. [+8]

Presence of primary neurological or autoimmune disorders. [+9]

Status: Recruiting

Home-Based Transcranial Direct Current Stimulation (tDCS) for Depression in Multiple Sclerosis (MS)

This project is a double-blind, sham-controlled, parallel-arm, randomized controlled trial. We will recruit n=170 people living with MS, who are experiencing an episode of depression in the context of a major depressive episode (MDE). Using our remotely supervised (RS) tDCS protocol, enrolled participants will complete 30 days of 30-minute tDCS (2.0, DLPFC left anodal) while listening to mindfulness meditation. Over the course of the study, participants will complete assessments of depression and MS symptoms. Participants will be randomized 1:1 active:sham tDCS.

Participants needed: 170
Trial details
Phase: Phase 2Age: 18-65Biological sex: AllType: InterventionalSponsor: NYU Langone HealthUpdated: Jun 29, 2026Locations: 1
Eligibility criteria

Age: 18-65 years (inclusive) [+5]

Neurological or Medical Disorders: History of primary neurological disorder othe... [+5]

Status: Not yet recruiting

Optimal Dosing of High-Intensity Locomotor Training for Step Attainment and Locomotor Outcomes in Stroke Patients Undergoing Acute Inpatient Rehabilitation

The purpose of this study is to elucidate optimal dosing for High Intensity Gait Training (HIGT) to reduce locomotor disability for those undergoing inpatient rehabilitation (IR) in the subacute phase of stroke recovery. This is a randomized controlled trial conducted at a single IR facility. Investigators will randomize patients to receive one of two distinct HIGT interventions or a high step count intervention during standard care.

Participants needed: 20
Trial details
Age: 18-95Biological sex: AllType: InterventionalSponsor: NYU Langone HealthUpdated: Jun 26, 2026Locations: 1
Eligibility criteria

Weightbearing restrictions, uncontrolled cardiopulmonary, metabolic, infectious,... [+3]

Status: Not yet recruiting

Phase 1 Study of WBRT or PCSI With REYOBIQ for Leptomeningeal Metastases

This Phase 1 study is designed to assess the safety, tolerability, and schedule feasibility of administering Rhenium-186 NanoLiposome (REYOBIQ) at different dosing intervals following whole brain radiotherapy (WBRT) or proton craniospinal irradiation (PCSI).

Participants needed: 29
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: NYU Langone HealthUpdated: Jun 29, 2026
Eligibility criteria

At least 18 years of age at screening [+13]

The subject has not recovered to National Cancer Institute (NCI) Common Terminol... [+8]

Status: Recruiting

Catch A Vibe - 24-00864

This study evaluates a proposed community-based implementation strategy to scale up screening, identification, and intervention on Health-Related Social Needs (HRSN) among persons on Long-Acting Injectable Pre-exposure Prophylaxis (LAI-PrEP). To do so, (1) screening for HRSN will occur at provider visits every 4 months, (2) navigation and establishment of connections with community resources through collaboration with two established community-based organization (CBO) partners, and (3) development of a tracking system integrated into the Electronic Medical Record (EMR) for monitoring and assessment of referral outcomes.

Participants needed: 343
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: NYU Langone HealthUpdated: Jun 26, 2026Locations: 2
Eligibility criteria

18 years of age or older [+21]

Less than 18 years old [+19]

Status: Recruiting

Clinical Evaluation of Frequency Allocation for Bimodal CI Users

This study will examine experienced, bimodal cochlear implant (CI) patients who receive an alternative frequency allocation table (FAT) to determine how it improves sound quality, device satisfaction, and speech perception abilities with respect to the standard default FAT. The goal of this study is to investigate how improving place-pitch mismatch in bimodal CI users affects 1) sound quality, 2) satisfaction, and 3) speech perception.

Participants needed: 13
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: NYU Langone HealthUpdated: Jun 26, 2026Locations: 1
Eligibility criteria

Age 18 or older [+8]

Under age 18 [+7]

Status: Recruiting

Smartphones for Opiate Addiction Recovery

Treatments for opioid addiction exist, but effectiveness is compromised when subjects use illicit opiates during treatment. Reuse rates during treatment can be high, and reducing illicit opiate use during treatment has thus recently become a major NIDA policy goal. The 5-minute battery indicates the numerical probability that a patient will reuse illicit opiates within the next 7-10 days.

Participants needed: 225
Trial details
Phase: Phase 3Age: 18-85Biological sex: AllType: InterventionalSponsor: NYU Langone HealthUpdated: Jun 23, 2026Locations: 2
Eligibility criteria

Meet DSM-5 criteria for opioid-use disorder (heroin and/or prescription opioids)... [+13]

Serious medical, psychiatric or non-opioid substance use disorder that, in the o... [+11]

Status: Recruiting

Evaluating the Effectiveness of a Colonoscopy Surveillance Recommendations Algorithm in Clinical Practice

The primary objective is to determine if the use of the colonoscopy surveillance recommendations algorithm increases the accuracy of surveillance timing recommendations compared to traditional methods. The secondary objective is to assess the time required to make surveillance recommendations with and without the algorithm, determine the efficiency gains (the average time saved per recommendation), and evaluate the opportunity cost (the financial value of the time saved).

Participants needed: 100
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: NYU Langone HealthUpdated: Jun 22, 2026Locations: 1
Eligibility criteria

Gastroenterologists and primary care physicians, including residents and fellows... [+1]

Physicians not practicing in relevant fields or those with conflicts of interest...

Status: Not yet recruiting

Postoperative Non-Opioid Pain Management Utilizing Local Anesthetics Coupled With Modulated Coagulation

This study is a prospective randomized trial examining the effect of tranexamic acid (TXA) and aminocaproic acid (ε-Ahx) with local anesthetics and thrombin in all electively created surgical wound beds in hand surgery to provide long term pain relief and decrease the use of postoperative narcotics. All surgical created wounds for any hand surgery will be treated in a randomized fashion with the following four arms: 1. Bupivacaine + lidocaine 2. Bupivacaine + lidocaine + thrombin 3. Bupivacaine + lidocaine + thrombin + tranexamic acid 4. Bupivacaine + lidocaine + thrombin + aminocaproic acid All are applied topically to surgical bed prior to closure of skin.

Participants needed: 40
Trial details
Phase: Phase 4Age: 18+Biological sex: AllType: InterventionalSponsor: NYU Langone HealthUpdated: Jun 12, 2026Locations: 1
Eligibility criteria

Age 18 or older [+1]

Any patient with a traumatic or infected open wound (only surgically created wou... [+15]

Status: Recruiting

Natural History Study of Synucleinopathies

Synucleinopathies are a group of rare diseases associated with worsening neurological deficits and the abnormal accumulation of the protein α-synuclein in the nervous system. Onset is usually in late adulthood at age 50 or older. Usually, synucleinopathies present clinically with slowness of movement, coordination difficulties or mild cognitive impairment. Development of these features indicates that abnormal alpha-synuclein deposits have destroyed key areas of the brain involved in the control of movement or cognition. Patients with synucleinopathies and signs of CNS-deficits are frequently diagnosed with Parkinson disease (PD), dementia with Lewy bodies (DLB) or multiple system atrophy (MSA). However, accumulation of alpha-synuclein and death of nerve cells can also begin outside the brain in the autonomic nerves. In such cases, syncucleinopathies present first with symptoms of autonomic impairment (unexplained constipation, urinary difficulties, and sexual dysfunction). In rare cases, hypotension on standing (a disorder known as orthostatic hypotension) may be the only clinical finding. This "pre-motor" autonomic stage suggests that the disease process may not yet have spread to the brain. After a variable period of time, but usually within 5-years, most patients with abnormally low blood pressure on standing develop cognitive or motor abnormalities. This stepwise evolution indicates that the disease spreads from the body to the brain. Another indication of this spread is that acting out dreams (i.e., REM sleep behavior disorder, RBD) a problem that occurs when the lower part of the brain is affected, may also be the first noticeable sign of Parkinson disease. The purpose of this study is to document the clinical features and biological markers of patients with synucleinopathies and better understand how these disorders evolve over time. The study will involve following patients diagnosed with a synucleinopathy (PD/DLB and MSA) and those believed to be in the "pre-motor" stage (with isolated autonomic impairment and/or RBD). Through a careful series of follow-up visits to participating Centers, we will focus on finding biological clues that predict which patients will develop motor/cognitive problems and which ones have the resilience to keep the disease at bay preventing spread to the brain. We will also define the natural history of MSA - the most aggressive of the synucleinopathies.

Participants needed: 800
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: NYU Langone HealthUpdated: Jun 10, 2026Locations: 8
Eligibility criteria

Both male and female patients will be included [+2]

Diabetes according to the American Diabetes Association criteria [+6]

Status: Recruiting

Influence of "Likes" in Social Media Food Ads on Black and White Adolescents' Food Purchases - Study 2

This is a randomized trial to examine the influence of number of "likes"on social media food ads on Black and White adolescents' food purchases

Participants needed: 1,300
Trial details
Age: 13-17Biological sex: AllType: InterventionalSponsor: NYU Langone HealthUpdated: Jun 10, 2026Locations: 1
Eligibility criteria

adolescent (13-17 years of age) who identifies as only non-Latino White or only...

Status: Recruiting

Effects of Racial Congruence, "Likes", and Food Images in Social Media Ads on Adolescents' Caloric Intake - Study 3

This is a randomized trial to to test the degree to which visual attention to unhealthy foods, racially congruent people, and/or "likes" in social media ads explains the relationship between ad exposure and calorie intake.

Participants needed: 480
Trial details
Age: 13-17Biological sex: AllType: InterventionalSponsor: NYU Langone HealthUpdated: Jun 10, 2026Locations: 1
Eligibility criteria

adolescent (13-17 years of age) who identifies as only non-Latino White or only...

- participants who do not meet all criteria described above

Status: Recruiting

tDCS: Sleep to Mood in Depression (S2M-D)

The purpose of this study is to determine whether changes in sleep consolidation occur during home-based transcranial direct current stimulation (tDCS) in adults with moderate depression and whether these changes are temporally associated with improvements in depressive symptoms.

Participants needed: 35
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: NYU Langone HealthUpdated: Jun 8, 2026Locations: 1
Eligibility criteria

Ability to read and understand study materials in English, as demonstrated by a... [+6]

Current major medical condition that, in the opinion of the study clinician, wou... [+7]

Status: Recruiting

Improving Food Access in East Flatbush Through a Community Partner Coalition in New York City (NYC)

The objective of this research study is to implement and evaluate a food pantry pilot program to improve access to food and overall diet quality in East Flatbush. This will be achieved through the implementation of a tailored, client-choice food pantry pilot program. The pilot program will specifically offer locally grown produce.

Participants needed: 250
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: NYU Langone HealthUpdated: Jun 9, 2026Locations: 1
Eligibility criteria

Adult at least 18 years old [+3]

Status: Recruiting

Cannabidiol (CBD) in Pain Reduction for Knee Osteoarthritis

The purpose of this study is to see if cannabidiol (CBD) orally dissolving tablets (ODTs) can lessen pain, improve function, and improve patient satisfaction in cases of knee osteoarthritis. CBD comes from the cannabis plant and is non-psychoactive (i.e. does not produce a 'high' or altered mental state) as compared to tetrahydrocannabinol (THC), another compound found in cannabis. Researchers are studying different forms of CBD for potential use in treating pain, inflammation, and illnesses.

Participants needed: 100
Trial details
Phase: Phase 2, Phase 3Age: 40-75Biological sex: AllType: InterventionalSponsor: NYU Langone HealthUpdated: Jun 9, 2026Locations: 1
Eligibility criteria

Patients presenting with knee osteoarthritis (KL Grade II-III) [+5]

Knee Injections within the last 3 months (cortisone, PRP, hyaluronic acid) [+23]

Status: Recruiting

Blood Flow Restriction Therapy in Achilles Injury

Blood flow restriction (BFR) therapy is a brief and partial restriction of venous outflow of an extremity during low load resistance exercises. It is a safe and effective method of improving strength in healthy and active individuals, recovering from orthopedic pathologies and procedures. This prospective, randomized study will look at the implications this form of treatment has on the rehabilitation of Achilles injuries.

Participants needed: 57
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: NYU Langone HealthUpdated: Jun 8, 2026Locations: 1
Eligibility criteria

Diagnosed with Achilles Injury [+2]

Patients with intention to receive standard therapy and not the study therapy [+4]

Status: Recruiting

The Effect of Yoga Practice on Chronic Back Pain

Chronic low back pain is notoriously difficult to treat and is a primary contributor to lost work days and excessive health expenditures, and whose treatment has, in part, contributed to the opioid crisis. Surgery is only an option in a minority of these patients, usually confined to those with structural instability. Yoga is an ancient modality whose benefits are currently being studied.

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: NYU Langone HealthUpdated: Jun 4, 2026Locations: 1
Eligibility criteria

Willingness to and ability to participate in study procedures [+1]

Indication for surgery (i.e., fracture, infection, scoliosis, spondylolisthesis) [+1]

Status: Recruiting

Risk Factors for Sudden Unexplained Death in Epilepsy

The main purpose of this study is to develop a North American registry for SUDEP cases; requesting family members of epilepsy patients who died suddenly of unclear causes (SUDEP) to contact the study team. The family members who decide to participate in the study will be asked to complete a brief telephone interview about their loved one's epilepsy and seizure history and the circumstances of his or her death. If the death has occurred within the past 24 hours, and the family is willing to consider donating tissue to the study, the subject will be transferred to the Autism Tissue Program, and the remainder of the phone interview will be conducted at a later time. In addition to the phone interview, the family will be asked to provide access to the deceased's medical records. Any costs involved in obtaining medical records will be covered by the study, and all medical information will remain completely confidential.

Participants needed: 800
Trial details
Biological sex: AllType: ObservationalSponsor: NYU Langone HealthUpdated: Jun 4, 2026Locations: 1
Eligibility criteria

Not listed

Status: Recruiting

Hirschsprung Disease Genetic Study

Hirschsprung disease is a genetic condition caused by lack of nerve cells in varying lengths of the intestines. This study will investigate the complex genetic basis of the disease, which involves multiple interacting genetic factors.

Participants needed: 3,000
Trial details
Age: 1-100Biological sex: AllType: ObservationalSponsor: NYU Langone HealthUpdated: Jun 4, 2026Locations: 1
Eligibility criteria

Unable or unwilling to provide sample for genetic studies [+1]