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NCT ID: NCT04972383 Completed - Knee Osteoarthritis Clinical Trials

Comparing Effect of Autologous Platelet-Rich Plasma Versus Hyaluronic Acid Treatment on Knee Osteoarthritis

Start date: November 7, 2017
Phase: Phase 3
Study type: Interventional

To compare the efficacy and structural change of intraarticular single platelet-rich plasma(PRP) versus novel crosslinked Hyaluronic Acid(HA)(HyajointPlus) for the treatment of early stage knee osteoarthritis(OA). This was a prospective, double-blind, RCT with an allocation ratio of 1:1.

NCT ID: NCT04971057 Completed - Pain Clinical Trials

Multimedia Information for Patients With Renal Biopsy

Start date: December 14, 2019
Phase: N/A
Study type: Interventional

This study takes place in the Divisions of Nephrology. Patients undergoing renal biopsy were randomized to control group or multimedia information intervention group. The control group received routine care, and the multimedia information intervention group received a multimedia information. After the pre-test, the two groups performed the 1 to 3 post-tests on pre-operation, post-operative day 1 and post-operative day 9. This study used questionnaires that including General Self-Efficacy Scale, Pain Visual Analogy Scale, Visual Analogue Scale for Anxiety, and Positive and Negative Affective Scale.

NCT ID: NCT04969952 Completed - Cancer Patients Clinical Trials

Evaluation of an Interventional Module to Assist Physicians Introducing ACP to Cancer Patients

Start date: April 6, 2021
Phase: N/A
Study type: Interventional

Evaluation of an Interventional module to assist physicians introducing ACP to cancer patients

NCT ID: NCT04968912 Completed - Sjogren's Syndrome Clinical Trials

A Study of Nipocalimab in Adults With Primary Sjogren's Syndrome (pSS)

Start date: September 21, 2021
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of nipocalimab in participants with primary Sjogren's syndrome (pSS) versus placebo.

NCT ID: NCT04967742 Completed - COVID-19 Clinical Trials

A Extension Study to Evaluate the Safety, Tolerability, and Immunogenicity of UB-612 COVID-19 Vaccine

Start date: August 5, 2021
Phase: Phase 1
Study type: Interventional

This is an extension study to evaluate the safety, tolerability and immunogenicity of one booster dose of UB-612 COVID-19 vaccine in adults who completed two vaccinations of UB-612 vaccine 10, 30, and 100 μg in V-122 study.

NCT ID: NCT04967261 Completed - Cardiology Clinical Trials

The Evaluation of Optimal Observation Period for Neurological Recovery in Post-arrest Survivors

Start date: August 1, 2021
Phase:
Study type: Observational

To explore whether the patient's neurological function recovery period is sufficient after successful emergency resuscitation recommended by the current guidelines

NCT ID: NCT04966364 Completed - Clinical trials for the Effect of Hypotension Prediction Index Application

Hypotension Prediction Index in Major Gastrointestinal Surgery

Start date: July 22, 2021
Phase: N/A
Study type: Interventional

Intraoperative hypotension (IOH) is defined as a mean arterial pressure (MAP) of < 65mmHg during surgery. Patients undergoing major gastrointestinal (GI) surgery, such as esophagectomy with reconstruction, are at a high-risk of IOH because such surgeries typically require more than 3h to complete and require blood transfusion or inotrope administration. Critically, these surgeries involve organ removal or substitute connection, which require wound or flap anastomosis. IOH is believed to be associated with postoperative anastomosis necrosis. It increases the risk of postoperative intrathoracic or abdominal infection, resulting in septic shock, postoperative major organ dysfunction and mortality. The data of TWA-MAP< 65mmHg in the HPI guidance group will be significantly lower than that in the group without HPI guidance.

NCT ID: NCT04966312 Completed - Surgery Clinical Trials

Preoperative Educational Videos Reduce Maternal Anxiety Whose Children Received Congenital Heart Disease Surgery

Start date: January 1, 2017
Phase: N/A
Study type: Interventional

To examine if educational digital video disk can reduce maternal anxiety and depression if their children undergo congenital heart disease surgery and when surgical or post-surgical complications occur. Compared to only routine education, adding digital video disk could decrease mothers' anxiety more after education, and until the day of discharge. Compared to only routine education, adding digital video disk could decrease mothers' anxiety more on the discharge day if their child had surgical or post-surgical complications.

NCT ID: NCT04966286 Completed - Quality of Life Clinical Trials

The Effectiveness of Applying Multimedia on Self-Care and Quality of Life in Patient With Enterostomy

Start date: June 1, 2018
Phase: N/A
Study type: Interventional

This report was an effective evaluation of using multimedia educational program for self-care and quality of life in patients with a stoma at postoperative and established a simple threshold for enterostomy self-care skills.

NCT ID: NCT04964908 Completed - Clinical trials for Chronic Lymphocytic Leukemia

Study to Understand Clinical Characteristics, Treatment Pathway in Chronic Lymphocytic Leukemia

CREEK
Start date: December 3, 2021
Phase:
Study type: Observational

A Multicenter Retrospective Study to understand the clinical characteristics, treatment pathway and resource utilization for patients with chronic lymphocytic leukemia A retrospective, multi-centre, observational study to describe disease characteristics, treatment patterns, treatment-related outcomes, and resource utilization for Chronic Lymphocytic Leukemia (CLL) patients in multiple international regions