Clinical Trial Search Results
Comparing Biceps and Triceps Muscle Oxygenation Using Near Infra-Red Spectroscopy in Healthy Participants using Blood Flow Restriction
This study is currently enrolling.
The purpose of the study is to assess and compare the muscle oxygenation in the biceps and triceps muscles with and without applying blood flow restriction on the arms of healthy individuals.
Concurrent Sports Hernia and Femoroacetabular Labral Repair – 2-year FU
This study is currently enrolling.
We aim to assess the clinical outcomes of concurrent sports hernia repair and femoroacetabular labral repair at a 2-year follow-up. We will compare pre-operative and post-operative scores and different time intervals. ...
Correlation Between the Number of Pain Pills and Pain level in Upper Extremity Surgery
This study is currently enrolling.
The purpose of the study is to investigate the effect of the number of pain relief pills on pain level and opioid refill request rate.
Correlation of Intraoperative Drop Test to Postoperative Range of Motion in Total Knee Arthroplasty
This study is currently enrolling.
The purpose of the study is to investigate the correlation between perioperative drop leg test and the final range of motion in primary total knee arthroplasty procedures.
CP-START-001: A Phase 1/2, First-in-Human, Open-Label, Dose Escalation and Expansion Study of STAR0602, a Selective T Cell Receptor (TCR)-targeting, Bifunctional Antibody-fusion Molecule, in Subjects with Unresectable, Locally Advanced, or Metastatic Solid Tumors that are Antigen-rich (START-001)
This study is currently enrolling.
The purpose of this research study is
CPO301-US-101: A Phase 1, Multicenter, Single Agent Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Evidence of Antitumor Activity of CPO301, an EGFR-Targeting Antibody-Drug Conjugate, in Adult Patients with Advanced or Metastatic Solid Tumors
This study is currently enrolling.
The purpose of the study, called CPO301-US-101, is to see if CPO301 (also known as SYS6010) is safe and effective in treating your type of cancer when administered as an intravenous (administered into the vein) infusion (IV) ov ...
CT-868-004
A Phase 2, Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Efficacy, Safety, Tolerability, and Pharmacokinetics of CT-868 Administered for 16 Weeks to Overweight and Obese Adult Participants with Type 1 Diabetes Mellitus
A Phase 2, Double-Blind, Randomized, Placebo-Controlled Study to Evaluate the Efficacy, Safety, Tolerability, and Pharmacokinetics of CT-868 Administered for 16 Weeks to Overweight and Obese Adult Participants with Type 1 Diabetes Mellitus
This study is currently enrolling.
Study Purpose: To evaluate the safety and tolerability of the study drug, CT-868, and to study the effect that CT-868 has on Type 1 Diabetes and weight. To be enrolled in this study, you must meet certain requirements. You may ...
D9075C00001: A Phase 3, Randomized, Double blind, Placebo controlled, Multicentre, International Study of Durvalumab and Domvanalimab (AB154) as Sequential Therapy in Participants with Locally Advanced (Stage III), Unresectable Non-small Cell Lung Cancer Whose Disease has not Progressed Following Definitive, Platinum-based Concurrent Chemoradiation Therapy (PACIFIC 8)
This study is currently enrolling.
This study is being carried out in stage III NSCLC which cannot be removed by surgery. In this study, we will identify the effectiveness and safety of a possible treatment combination – durvalumab with domvanalimab, comparing t ...
DiuRetics Alone vs. AortIx ENdovascular Device for Acute Heart Failure (DRAIN HF)
This study is currently enrolling.
ENROLLING IN TAMPA, FL - The purpose of this research is to evaluate the investigational Aortix System. The Aortix System is not approved by the FDA. The system has been designed for use in patients hospitalized with heart fail ...