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NCT ID: NCT03952715 Recruiting - Healthy Clinical Trials

Can Training Increase Reporting Accuracy and Study Power in Human Pain Trials

Start date: April 17, 2018
Phase: N/A
Study type: Interventional

In previous studies, results of both the Focused Analgesia Selection Test (FAST) procedure, a method to assess pain-reporting accuracy, and the Evoked Pain Training (EPT) procedure, aimed to improve pain-reporting accuracy, correlated with the placebo response. The objectives of the current project were to determine if EPT (1) increases pain reporting accuracy and (2) affect the placebo response in experimental pain study.

NCT ID: NCT04145245 Recruiting - Patient Compliance Clinical Trials

A Randomized Controlled Trial to Assess the Effect of L-carnitine in Patients With Diabetic Peripheral Neuropathy to Relief Pain and Symptom Improvement

Start date: April 17, 2018
Phase: Phase 2
Study type: Interventional

Diabetic Peripheral Neuropathy (DPN) is a common complication of diabetes mellitus. The prevalence rate is approaching towards a peak throughout the world including Bangladesh. The current intervention used in peripheral neuropathy does not bring satisfactory result. Recent trial shows that L-carnitine is effective and safe in DPN. So it is expected that L-carnitine may produce better effect in compared to other medicine used previously for alleviation of DPN.

NCT ID: NCT04404322 Recruiting - Suicide, Attempted Clinical Trials

Ultra - Brief Crisis IPT-A Based Intervention for Suicidal Children and Adolescents (IPT-A-SCI)

Start date: April 17, 2018
Phase: N/A
Study type: Interventional

To address the critical need in crisis intervention for children and adolescents at suicidal risk the investigators developed an ultra-brief acute crisis intervention, based on Interpersonal Psychotherapy (IPT). The current adaptation of IPT-A is comprised of five weekly sessions, followed by monthly follow-up caring email contacts to the patients and their parents, over a period of three months.

NCT ID: NCT04408859 Recruiting - Clinical trials for QOL; Quality of Life;Gastric Cancer; Gastrectomy;Neoadjuvant Chemotherapy

Quality of Life in Advanced Gastric Cancer Patients Receiving Neoadjuvant Chemotherapy

Start date: April 17, 2018
Phase:
Study type: Observational

The purpose of this study is to explore the influence of neoadjuvant chemotherapy in the long term quality of life with advanced gastric cancer patients.

NCT ID: NCT03197480 Recruiting - Clinical trials for Diabetic Macular Edema

Diabetic Macular Edema Asian Response (DEAR) Study: Biomarkers for Response to Aflibercept in Asian Patients With Center Involving DME

Start date: April 17, 2019
Phase: Phase 4
Study type: Interventional

To investigate whether ocular imaging and proteomic biomarkers; and systemic biochemical, metabolomic, and genetic biomarkers predict treatment response to intravitreal aflibercept in a cohort of patients with DME.

NCT ID: NCT03384433 Recruiting - Clinical trials for Cerebrovascular Disorders

Allogenic Mesenchymal Stem Cell Derived Exosome in Patients With Acute Ischemic Stroke

Start date: April 17, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

Administration of cell-free exosomes derived from mesenchymal stem cell (MSCs) can be sufficient to exert therapeutic effects of intact MSCs after brain injury. In this study we aim to assay the administration of MSC derived exosome on improvement of disability of patients with acute ischemic stroke

NCT ID: NCT03519269 Recruiting - Clinical trials for Osteoarthritis, Knee

Navio Robotic Versus Conventional Total Knee Arthroplasty

Start date: April 17, 2019
Phase: N/A
Study type: Interventional

Total knee replacement surgery is a conventional approach to alleviating the pain and lack of function resulting from arthritis of the knee. While conventional knee replacement surgery is highly successful, incidences of improperly installed replacement parts are not uncommon. To improve outcomes, robotic-assisted total knee replacement surgery has recently become available, and has been shown to be extremely effective for partial knee replacement surgery. However, further research is needed to determine if this same technology can be equally effective for total knee replacement surgery. The present study will evaluate outcomes of robotic-assisted versus conventional total knee replacement surgery in patients between 40 and 85 years old with end stage arthritis of the knee. Other than surgical technique, patients will receive the same operative care and knee replacement implants. In addition to standard x-rays, subjects will be asked to complete several short-term clinical and functional tests and questionnaires to determine outcomes of their surgery.

NCT ID: NCT03545386 Recruiting - Pouchitis Clinical Trials

Fecal Microbiota Transplantation for Pouchitis

Start date: April 17, 2019
Phase: Phase 2
Study type: Interventional

This is a randomized double-blind placebo controlled trial involving a single centre (McMaster University) recruiting patients from Hamilton, ON and the surrounding regions, to evaluate whether fecal microbiota transplantation once weekly for six weeks increases the remission rate compared to placebo in patients with active pouchitis.

NCT ID: NCT03718637 Recruiting - Clinical trials for Lateral Epicondylitis

Efficacy Bioinductive Implant for Tennis Elbow (Lateral Epicondylitis)

Start date: April 17, 2019
Phase: Phase 4
Study type: Interventional

The investigators are testing the efficacy of a new, FDA-approved bioinductive patch in lateral epicondylitis (tennis elbow) patients. A bioinductive patch is an implant that may foster tendon regrowth and healing following surgery. Patients will be randomize into one of two groups: control and investigational. Patients in the "control group" will receive the normal surgery for patients who do not respond to physical therapy, lifestyle changes, and anti-inflammatory treatment. Patients in the "experimental group" will receive the same surgical treatment, with the addition of the bioinductive patch. This patch will be implanted during surgery. Then, using a combination of ultrasound studies and other measures, the investigators will assess how well the patch works compared to surgery alone.

NCT ID: NCT03850899 Recruiting - Alcoholic Hepatitis Clinical Trials

Alcoholic Hepatitis Network Observational Study

Start date: April 17, 2019
Phase:
Study type: Observational

The purpose of this research study is to create a clinical database and bio-repository. To do this, we will obtain blood, urine, saliva, and stool samples (e.g., biological samples) and personal health information from you to use in future research studies related to alcoholic hepatitis or other diseases. Part of your blood sample will be used to extract your DNA. DNA is the genetic material that gives us unique characteristics. We are doing this research study because we are trying to find out more about how and why illnesses related to alcoholic hepatitis or other diseases occur in people. To do this, we will study the biological samples and personal health information from healthy and sick people. A "biological sample" is usually blood, but can be any body fluid. "Personal Health Information" includes such items as your name, age, gender, race, and/or your medical information. It can also include data from measurements and tests that you had while participating in another research study or that were done during the course of your regular medical care or doctor visits.