The state of Illinois currently has 18 active clinical trials seeking participants for Healthy research studies. These trials are conducted in various cities, including Chicago, Peoria, Springfield and Urbana.
Study to Assess Adverse Events and How ABBV-932 Oral Capsules Moves Through the Body of Healthy Adult Participants
Recruiting
The main objective of this study is to assess pharmacokinetics, safety, and tolerability of ABBV-932 in healthy adult participants.
Gender:
All
Ages:
Between 18 years and 65 years
Trial Updated:
03/22/2024
Locations: Acpru /Id# 249639, Grayslake, Illinois
Conditions: Generalized Anxiety Disorder (GAD), Healthy Participants
Improving Human Cerebrovascular Function Using Acute Intermittent Hypoxia
Recruiting
This study uses magnetic resonance imaging to determine whether 3 weeks of repeated exposure to Acute Intermittent Hypoxia can improve brain blood flow or blood flow regulation in healthy adults.
Gender:
All
Ages:
Between 21 years and 50 years
Trial Updated:
03/12/2024
Locations: Northwestern University, Chicago, Illinois
Conditions: Healthy Brain Perfusion
Plants Optimizing Development Study (PODS)
Recruiting
This study aims to conduct a randomized clinical trial to measure the effects of a 3-month daily mixed-soy food intervention vs. a control group receiving isocaloric foods on reproductive hormones, body composition, metabolic risk, fecal microbiota, and cognition among 8-11-year-old children. Additionally, this study will assess soy food intake immediately following participation in the clinical trial to determine changes in soy food acceptance in children.
Gender:
All
Ages:
Between 8 years and 11 years
Trial Updated:
03/07/2024
Locations: University of Illinois, Urbana, Illinois
Conditions: Healthy Children
Integrated Cancer Repository for Cancer Research
Recruiting
The iCaRe2 is a multi-institutional resource created and maintained by the Fred & Pamela Buffett Cancer Center to collect and manage standardized, multi-dimensional, longitudinal data and biospecimens on consented adult cancer patients, high-risk individuals, and normal controls. The distinct characteristic of the iCaRe2 is its geographical coverage, with a significant percentage of small and rural hospitals and cancer centers. The iCaRe2 advances comprehensive studies of risk factors of cancer... Read More
Gender:
All
Ages:
Between 19 years and 110 years
Trial Updated:
02/29/2024
Locations: Rush-Copley Cancer Care Center, Aurora, Illinois +2 locations
Conditions: Pancreatic Cancer, Thyroid Cancer, Lung Cancer, Esophageal Cancer, Thymus Cancer, Colon Cancer, Rectal Cancer, Anal Cancer, Bile Duct Cancer, Duodenal Cancer, Gallbladder Cancer, Gastric Cancer, Liver Cancer, Small Intestine Cancer, Peritoneal Surface Malignancies, Familial Adenomatous Polyposis, Lynch Syndrome, Bladder Cancer, Kidney Cancer, Penile Cancer, Prostate Cancer, Testicular Cancer, Ureter Cancer, Urethral Cancer, Hypopharyngeal Cancer, Laryngeal Cancer, Lip Cancer, Oral Cavity Cancer, Nasopharyngeal Cancer, Oropharyngeal Cancer, Paranasal Sinus Cancer, Nasal Cavity Cancer, Salivary Gland Cancer, Skin Cancer, Mesothelioma, Breast Cancer, Leukemia, Melanoma, Sarcoma, Unknown Primary Tumor, Multiple Myeloma, Ovarian Cancer, Endometrial Cancer, Vaginal Cancer, Neuroendocrine Tumors, Plasma Cell Dyscrasia, Healthy Control, Gastrointestinal Stromal Tumors, Central Nervous System Tumor, Central Nervous System Cancer
Study of an Investigational Pentavalent Meningococcal ABCYW Vaccine in Adults and Adolescents
Recruiting
The purpose of VAN00010 study is to assess the safety and immunogenicity of the investigational pentavalent meningococcal ABCYW vaccine in adults and adolescents. The study duration will be up to 12 months for all participants.
Gender:
All
Ages:
Between 10 years and 25 years
Trial Updated:
02/20/2024
Locations: AES Peoria Site Number : 8400090, Peoria, Illinois
Conditions: Meningococcal Infection, Healthy Volunteers
Mechanical Coring to Achieve Directional Skin Tightening
Recruiting
The objective of this clinical study is to evaluate the safety and efficacy of mechanical coring for directional skin tightening. This study is a prospective, up to 3 center, multiple skin treatment area study of the safety and efficacy of mechanical coring with directional closure to achieve directional skin tightening.
Gender:
All
Ages:
Between 30 years and 70 years
Trial Updated:
02/13/2024
Locations: DeNova Research, Chicago, Illinois
Conditions: Skin Tightening, Healthy Volunteers
A Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of ABBV-932 in Healthy Adult Participants, Participants With Generalized Anxiety Disorder (GAD) and Participants With Bipolar Disorder (BPD)
Recruiting
The purpose of this study is to assess the pharmacokinetics, safety, and tolerability following multiple ascending oral doses of ABBV-932 or placebo in healthy adult participants, participants with Generalized Anxiety Disorder (GAD), and participants with bipolar disorder (BPD).
Gender:
All
Ages:
Between 18 months and 65 years
Trial Updated:
02/12/2024
Locations: Acpru /Id# 255945, Grayslake, Illinois
Conditions: Healthy Volunteers, Generalized Anxiety Disorder (GAD), Bipolar Disorder (BPD)
A Study to Evaluate Adverse Events and How Single Ascending Doses of ABBV-141 Move Through the Body of Healthy Adult Western and Asian Participants
Recruiting
The purpose of this study is to assess the safety, tolerability, pharmacokinetics (PK) and immunogenicity after single ascending doses (SAD) of ABBV-141 in healthy adult Western and Asian participants.
Gender:
All
Ages:
Between 18 years and 55 years
Trial Updated:
01/31/2024
Locations: Acpru /Id# 261162, Grayslake, Illinois
Conditions: Healthy Volunteers
A Study of TAK-279 in Adults With or Without Kidney Problems
Recruiting
The main aim of this study is to find out how the body processes 1 dose of TAK-279 (pharmacokinetics) in participants with kidney problems compared to participants without kidney problems. Other aims are to check for side effects from TAK-279 and to learn how well participants tolerate 1 dose of TAK-279. The participants will need to stay at the clinic for 11 days.
Gender:
All
Ages:
18 years and above
Trial Updated:
11/21/2023
Locations: Research by Design, Chicago, Illinois
Conditions: Renal Impairment, Healthy Volunteers
Testing the Contribution of Orbitofrontal Cortex Networks to Decision-making
Recruiting
This research study examines the contribution of orbitofrontal cortex (OFC) networks to decision-making.
Gender:
All
Ages:
Between 18 years and 40 years
Trial Updated:
11/08/2023
Locations: Northwestern University, Chicago, Illinois
Conditions: Healthy
The Gut and Skin Microbiome in Vitiligo Disease Progression
Recruiting
Investigators plan to perform a pilot study that aims to characterize the microbiome of human vitiligo patients with both active and stable disease and compare this to the microbiome of age and sex matched controls. The investigators aim to answer the question whether the gut and skin microbiome of patients with vitiligo differs from the general population.
Gender:
All
Ages:
Between 18 years and 89 years
Trial Updated:
11/07/2023
Locations: Northwestern University, Chicago, Illinois
Conditions: Vitiligo, Healthy
A Study to Assess Food Effect of Venetoclax New Tablet Formulation in Healthy Female Participants
Recruiting
The purpose of this study is to assess the bioavailability of two different doses of venetoclax new high drug load formulation tablets relative to two tablets of the currently marketed venetoclax tablets under fed conditions.
Gender:
Female
Ages:
Between 18 years and 65 years
Trial Updated:
10/02/2023
Locations: Acpru /Id# 259897, Grayslake, Illinois
Conditions: Healthy Volunteers