Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.
This study will collect longitudinal biological samples and survey data to identify the triggers of IBD flares.
Patient at Universidade Federal de Santa Catarina (UFSC) Hospital, under care of...
Cancer Diagnosis/Treatment [+1]
The goal of this observational study is to identify molecular features in multiple clinical samples and/or the patient environment that are associated with ALS. Participants will collect biological samples and answer questionnaires regarding their health at each appointment with their ALS practitioner.
Patient of Dr. Espíndola at UFSC
US residents who have mental health issues sign the informed consent form and are screened and enrolled for this study. Participants complete a survey upon enrollment and are randomized into one of two study arms. This study is direct to participant and will NOT utilize clinical sites.
Resident of the United States [+6]
Unwilling to change their current diet [+21]
A total of at least 1,000 participants with suspicion of cancer including at least 107 subjects who will be diagnosed with OSCC or OPSCC will be enrolled from either primary or secondary care centers in the U.S. Clinicians will use Viome collection kits to collect saliva samples from eligible patients.
Signed and dated informed consent prior to any study-specific procedures are per... [+3]
Pregnancy [+1]
This is a randomized, placebo-controlled trial that will test the efficacy of VPNP in reducing HbA1c. Participant recruitment will occur through direct-to-participant enrollment. No additional clinical sites will be used for recruitment.
Signed and dated informed consent form and medical release prior to any trial-sp... [+6]
Antibiotic use within one month of the GI test [+9]
US residents who have obesity and sign the informed consent form and are screened and enrolled for this study. Participants who are enrolled complete a survey upon enrollment and are randomized into one of three arms. This study is direct to participant and will not utilize clinical sites.
Resident of the United States [+6]
Unwilling to change current diet [+22]
To evaluate the design, safety and efficacy of OralViome Cancer Testing system in the early detection of Oral and Throat Cancers using saliva metatranscriptomic analysis. This study will recruit only at existing clinical sites and will NOT use any additional clinical sites.
Signed Informed Consent obtained [+2]
Pregnancy [+1]
US residents who have gastrointestinal issues sign the informed consent form and are screened and enrolled for this study. Participants who are enrolled complete a survey upon enrollment and are randomized into one of three arms. This study is direct to participant and will NOT utilize clinical sites.
Resident of the United States [+6]
Unwilling to change current diet [+14]
30 participants with advanced or recurrent gynecological cancer from are enrolled for this study. Eligible participants then provide fecal specimen, blood, vaginal swab, oral mucosal swab and receive food dietary recommendation. Additional samples are collected for results analysis.
Adult females > 18 years old [+2]
Patients unable to provide fecal specimens at three time points [+6]
This is a randomized, placebo-controlled trial that will test the efficacy of VPNP in reducing HbA1c. Participant recruitment will occur through direct-to-participant enrollment. No additional clinical sites will be used for recruitment.
Signed and dated informed consent form and medical release prior to any trial-sp... [+6]
Antibiotic use within one month of the GI test [+9]
The purpose of the study is to collect and analyze physiological, physical, and molecular data from a diverse population to increase our understanding of how such parameters are associated with health and disease.
Anyone that resides in the US at the time of enrollment.
None