Kamigyo-ku, Japan Clinical Trials

A listing of Kamigyo-ku, Japan clinical trials actively recruiting patients volunteers.

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Found 23 clinical trials
Safety and Effectiveness of Agent Paclitaxel-Coated PTCA Balloon Catheter. (AGENT Japan SV)

A Randomized Trial Comparing the Agent Paclitaxel-Coated PTCA Balloon Catheter vs SeQuent Please Drug Eluting Balloon Catheter for the Treatment of a Small Vessel De Novo Native Coronary Artery Lesion.

bypass graft
in stent restenosis
percutaneous coronary intervention
Kyoto-Katsura Hospital
 (5.1 away) Contact site
  • 02 May, 2021
  • +13 other locations
Isolation Procedure vs. Conventional Procedure During Distal Pancreatectosplenectomy for Pancreatic Cancer

In the distal pancreatectomy (including pancreatic tail resection) for invasive ductal carcinoma of the pancreas, we evaluate the usefulness of a procedure of firstly transection of splenic arteries and veins (the isolation procedure group) compared to a conventional procedure of transection of the splenic vein at the end.

Shiga Medical University
 (5.6 away) Contact site
  • 26 Jan, 2021
  • +9 other locations
Observational Study of Patients With Moderate to Severe Chronic Plaque Psoriasis

This study will assess the use of risankizumab in adult patients with moderate to severe chronic plaque psoriasis and compare risankizumab to other commonly used biologics.

University Hospital Kyoto Prefectural University of Medicine /ID# 213396
 (0.8 away) Contact site
  • 02 Feb, 2021
  • +286 other locations
Indication and Treatment of Adult Kyphoscoliosis

Degeneration, iatrogenic-/idiopathic causes and fractures can lead to kypho- scoliotic deformities potentially resulting in pain and loss of function. The surgical strategies rely on surgeon preferences and type of deformity as well as clinical symptoms. The complication rate of surgical treatment is high. The aim of this study is to …

Kyoto University Hospital
 (1.3 away) Contact site
  • 23 Feb, 2021
  • +4 other locations
Special Drug Use Observational Study of Xolair in Patients With Severe to Most Severe Seasonal Allergic Rhinitis Aged 12 Years and < 18 Years Whose Symptoms Were Inadequately Controlled Despite to Conventional Therapies

This is a multicenter, uncontrolled, open-label, special drug use study to investigate the safety and efficacy of Xolair by collecting data in its clinical setting in patients with severe to most severe seasonal allergic rhinitis aged 12 years and < 18 years whose symptoms were inadequately controlled despite to conventional …

Novartis Investigative Site
 (1.4 away) Contact site
  • 24 May, 2021
  • +14 other locations
IMFINZI Study in Patients With Extensive Stage Small Cell Lung Cancer

To capture safety(FN) when IMF is administered to patients with extensive stage small cell lung cancer in clinical practice after launch

Research Site
 (5.1 away) Contact site
  • 12 Jun, 2021
  • +38 other locations
Pompe Disease Registry Protocol

The Pompe Registry is a global, multicenter, international, longitudinal, observational, and voluntary program for patients with Pompe disease, designed to track the disease's natural history and outcomes in patients, both treated and not. Data from the Registry are also used to fulfill various global regulatory commitments, to support product development/reimbursement, …

replacement therapy
gaa gene
alglucosidase alfa
Investigational Site Number 392106
 (9.7 away) Contact site
  • 28 Jan, 2021
  • +279 other locations
Product Performance Report: Evaluate Long-term Reliability & Performance of Medtronic Marketed Cardiac Therapy Products

The main purpose of the Product Performance Report (formerly referred to as System Longevity Study) is to evaluate long-term performance of Medtronic market-released cardiac rhythm products by analyzing product survival probabilities.

 (1.4 away) Contact site
  • 04 Jun, 2021
  • +227 other locations
3T MRI CIED Post-Approval Study

The purpose of this study is to evaluate product performance of Magnetic Resonance (MR) Conditional Cardiac Implantable Electronic Devices (CIED) following 3 tesla (3T) MRI exposure. This will be achieved by evaluating the changes in pacing capture threshold (PCT) measurements following 3T MRI scan exposure. This study is required by …

 (1.4 away) Contact site
  • 02 Jun, 2021
  • +142 other locations
Brilinta Clinical Experience Investigation

To confirm the following safety topics in patients to be treated with BRILINTA tablets 60 mg or 90 mg (hereinafter referred to as "BRILINTA") in clinical practice in the post-marketing phase. Profile and incidence of ADRs The CEI will be conducted to collect data of the events, especially focusing on …

Research Site
 (1.4 away) Contact site
  • 26 Apr, 2021
  • +31 other locations