A listing of All Conditions medical research trials actively recruiting patient volunteers. Search for closest city to find more detailed information on a research study in your area.
See below. To characterize the patterns of longitudinal change in brain volume, white matter myelin content, and measures of NVU function (cerebral blood flow (CBF), CVR, BBB permeability, and extracellular free water) over the first 3 years following TBI. To determine the prognostic value of NVU measures (CBF, CVR, BBB …
Please refer to section 3 of the study protocol. Penn will only enroll participants into Part 3 of the study. PRIMARY OBJECTIVES The primary objective of Part 1 is to assess the safety, tolerability, and manufacturing feasibility of Descartes-08 in patients with GMG. Part 1 of the study follows an …
To evaluate the safety, tolerability, and recommended Phase 2 dose (RP2D) of magrolimab in combination with bevacizumab and FOLFIRI (5-fluorouracil [5-FU], irinotecan, and leucovorin [LV]) in previously treated patients with advanced inoperable metastatic colorectal cancer (mCRC). We would like to rely on Advarra as the IRB of record for this …
Primary Objective: To determine if CONDUIT and PEEK +rhBMP-2 cages produce similar clinical and radiographic outcomes in patients undergoing direct lateral Interbody fusion Secondary Objective: To determine if CONDUIT and PEEK + rhBMP-2 cages are comparable with regards to cost The primary study endpoint will be the difference in fusion …
Please refer to Protocol Section 3 (Objectives and Endpoints). Please refer to Protocol Section 3 (Objectives and Endpoints). Please refer to Protocol Section 3 (Objectives and Endpoints).
The purpose of this study is to better understand molecular pathways and joint destruction in patients with autoimmune diseases such as Psoriatic Arthritis (PsA).
The Aim of this study is to validate community-based use of the haptic robot gym. We will test the safety of the haptic robot gym in a community-based rehabilitation setting. Milestones are 1) to quantify the safety of the system in terms of adverse events frequency and characteristics, 2) to …
A single site, 3-arm (CBT-I group; Bright Light Therapy group; Standard of Care group), parallel, randomized controlled trial in subjects with insomnia, fatigue and PAH will be conducted. Primary Objective To assess the feasibility (recruitment and retention rates) of CBT-I and Bright Light Therapy in patients with PAH. Secondary Objectives …
To compare the progression-free survival in participants with relapsed/refractory large B-cell lymphoma or follicular lymphoma grade 3B with stable disease (SD) or partial remission (PR) on first imaging response by central review (day +30PET/CT scan) after commercial CD19 CAR T-cell therapy
This is a prospective cohort study to document long-term dental and other oral outcomes in patients who receive external beam and modern radiation therapy (RT) modalities with curative intent, as part of clinical care for a head and neck cancer. ORARAD II study will examine participants of the original cohort …