There are currently 46 clinical trials in Lafayette, Louisiana looking for participants to engage in research studies. Trials are conducted at various facilities, including GSK Investigational Site, Romagosa Radiation Oncology Center, 1160.26.0018 Boehringer Ingelheim Investigational Site and Cardiovascular Institute of the South. Whether you're a healthy volunteer looking to participate in paid medical research or seeking trials related to a specific condition, the city provides a diverse range of opportunities near you.
A Prospective Single-Arm Multicenter StuDy of the BarE TEmporary SPur StEnt System foR the tREatment of Vascular Lesions Located in the infrapoplitEal Arteries beLow the Knee (DEEPER REVEAL)
Recruiting
This is a prospective, multicenter, single arm study designed to evaluate the safety and efficacy of the Temporary Bare Spur Stent System (Spur Stent System).
Gender:
All
Ages:
18 years and above
Trial Updated:
01/26/2024
Locations: Cardiovascular Institute of the South, Lafayette, Louisiana
Conditions: Peripheral Arterial Disease, Critical Limb Ischemia
A Phase 3 Study Evaluating Efficacy and Safety of Lanifibranor Followed by an Active Treatment Extension in Adult Patients With (NASH) and Fibrosis Stages F2 and F3 ( NATiV3 )
Recruiting
This Phase 3 study is conducted to evaluate lanifibranor in adults with NASH and liver fibrosis histological stage F2 or F3
Gender:
All
Ages:
18 years and above
Trial Updated:
01/24/2024
Locations: Combined Gastro Research LLC, Lafayette, Louisiana
Conditions: NASH - Nonalcoholic Steatohepatitis
Phase 2a To Evaluate PL-8177 in Subjects With Active Ulcerative Colitis (UC)
Recruiting
The purpose of this study is to compare PL8177 (a melanocortin receptor agonist) to placebo (in a 3:1 ratio-meaning that for every 3 people that get the active drug, one will receive placebo). The study treatment will be for 8 weeks. The study will measure safety and the body's ability to handle PL8177 and look at the improvement and healing of the intestine after 8 weeks of treatment. The study will include adult males and nonpregnant, nonlactating females with acute Ulcerative Colitis (UC).
Gender:
All
Ages:
Between 18 years and 75 years
Trial Updated:
01/08/2024
Locations: Gastroenterology Clinic of Acadiana, Lafayette, Louisiana
Conditions: Ulcerative Colitis, Ulcerative Colitis Acute, Ulcerative, Ulcerative Colitis Flare
A Study to Evaluate EDP 938 Regimens in Children With RSV
Recruiting
A 2-part study to evaluate the safety, pharmacokinetics and efficacy of EDP-938 in children with RSV infection.
Gender:
All
Ages:
Between 28 days and 36 months
Trial Updated:
01/04/2024
Locations: MedPharmics - Lafayette, Lafayette, Louisiana
Conditions: Respiratory Syncytial Virus (RSV)
Post-approval Study of Transcarotid Artery Revascularization in Standard Risk Patients With Significant Carotid Artery Disease
Recruiting
The study objective is to evaluate real world usage of the ENROUTE Transcarotid Stent when used with the ENROUTE Transcarotid Neuroprotection System in patients at standard risk for adverse events from carotid endarterectomy
Gender:
All
Ages:
Between 18 years and 79 years
Trial Updated:
11/15/2023
Locations: Acadiana Vascular Clinic / Our Lady Lourdes Heart Hospital, Lafayette, Louisiana
Conditions: Carotid Artery Diseases
Misago® RX Self-expanding Peripheral Stent for Common and/or External Iliac Artery
Recruiting
This is a multi-center, single arm, non-randomized, prospective clinical study using the Misago® RX Self-expanding Peripheral Stent for treatment of de novo, restenotic, and/or occlusive lesion(s) of the common and/or external iliac artery.
Gender:
All
Ages:
18 years and above
Trial Updated:
10/25/2023
Locations: Cardiovascular Institute of the South, Lafayette, Louisiana
Conditions: Iliac Artery Stenosis
A Study of EDP-938 in Non-hospitalized Adults With RSV Who Are at High Risk for Complications.
Recruiting
This is a Phase 2b, randomized, double-blind, placebo-controlled study of EDP-938 administered orally for the treatment of non-hospitalized adult subjects with confirmed RSV infection who are at high risk for complications after RSV infection.
Gender:
All
Ages:
18 years and above
Trial Updated:
09/12/2023
Locations: Velocity Clinical Research - Covington - PPDS, Lafayette, Louisiana
Conditions: RSV Infection
Phase 2 Clinical Trial of CartiLife® in the United States
Recruiting
To evaluate the safety and efficacy of implanting pellet-type extracellular matrix-associated autologous chondrocytes (CartiLife®) obtained by cultivating costal chondrocytes of the subject with articular cartilage defects of the knee as a result of trauma or degeneration.
Gender:
All
Ages:
18 years and above
Trial Updated:
08/24/2023
Locations: Lafayette General Health, Lafayette, Louisiana
Conditions: Articular Cartilage Defect, Articular Cartilage Degeneration
Prospective Research Assessment in Multiple Myeloma: An Observational Evaluation (PREAMBLE)
Recruiting
The purpose of this study is to assess the clinical effectiveness of all approved multiple myeloma (MM) therapies in the newly-diagnosed (NDMM) and the relapsed/refractory MM (RRMM) settings in real-world clinical practice.
Gender:
All
Ages:
18 years and above
Trial Updated:
02/16/2023
Locations: Cancer Center of Acadiana at Lafayette General Health, Lafayette, Louisiana +1 locations
Conditions: Multiple Myeloma
Diagnostic Accuracy and Safety of DBV1605 for the Diagnosis of Non-IgE Mediated Cow's Milk Allergy in Children
Recruiting
Study to assess the diagnostic accuracy (sensitivity, specificity, positive and negative predictive value) of DBV1605 for the diagnosis of non-Immunoglobulin E (IgE) mediated cow's milk allergy (CMA) in children with symptoms suggestive of non-IgE mediated CMA.
Gender:
All
Ages:
Between 29 days and 24 months
Trial Updated:
08/09/2022
Locations: MedPharmics, LLC - Lafayette, Lafayette, Louisiana
Conditions: Cow's Milk Allergy