Coronary Artery Disease Clinical Trial
Official title:
Laser Hemotherapy Trial for Coronary Artery Disease Prevention in High Risk Patients
Verified date | February 2019 |
Source | Cairo University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study will evaluate the effect of low level laser blood radiation applied to all participants for prevention of coronary artery disease in patients with high risk (hypertension,high blood viscosity, hypercholesterolemia as well as related immune issues)
Status | Completed |
Enrollment | 50 |
Est. completion date | December 30, 2018 |
Est. primary completion date | August 5, 2018 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 55 Years to 65 Years |
Eligibility |
Inclusion Criteria: - stage I hypertensive patients - patients from 30 to 34.9 kg/m2 body mass index - medically stable patients - all participants have sufficient cognition enough to understand the requirements of the study Exclusion Criteria: - history of malignant disease - smoking - history of progressive fatal disease - history of drug or alcohol abuse - blood donation within at least 30 days - pregnant, trying to be pregnant or breast feeding - cognitive impairment that will make it difficult to partake in the study |
Country | Name | City | State |
---|---|---|---|
Egypt | Cairo | Giza | Dokki |
Lead Sponsor | Collaborator |
---|---|
Cairo University |
Egypt,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | changes of blood pressure | measuring blood pressure before and after each low level laser radiation | 8 weeks | |
Secondary | changes in blood viscosity | measuring changes in blood viscosity before and after low level laser radiation session | 8 weeks | |
Secondary | change in IL-17 level | measuring changes in IL-17 level before and after low level laser radiation session | 45 days | |
Secondary | change in functional capacity | measuring of 6 minute walking test before and after low level laser irradiation as an indicator of functional capacity improving | 70 days | |
Secondary | change in CD 8 (cluster of differentiation 8) level | measuring changes in CD 8 (cluster of differentiation 8) level before and after low level laser radiation session | 45 days | |
Secondary | change in TC (total cholesterol) level | measuring changes in TC (total cholesterol) level before and after low level laser radiation session | 60 days | |
Secondary | change in LDL (low density lipoprotien) level | measuring changes in LDL (low density lipoprotien) level before and after low level laser radiation session | 60 days | |
Secondary | change in TG (triglyceride) level | measuring changes in TG (triglyceride) level before and after low level laser radiation session | 60 days | |
Secondary | change in HDL (high density lipoprotien) level | measuring changes in HDL (high density lipoprotien) level before and after low level laser radiation session | 60 days |
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT06030596 -
SPECT Myocardial Blood Flow Quantification for Diagnosis of Ischemic Heart Disease Determined by Fraction Flow Reserve
|
||
Completed |
NCT04080700 -
Korean Prospective Registry for Evaluating the Safety and Efficacy of Distal Radial Approach (KODRA)
|
||
Recruiting |
NCT03810599 -
Patient-reported Outcomes in the Bergen Early Cardiac Rehabilitation Study
|
N/A | |
Recruiting |
NCT06002932 -
Comparison of PROVISIONal 1-stent Strategy With DEB Versus Planned 2-stent Strategy in Coronary Bifurcation Lesions.
|
N/A | |
Not yet recruiting |
NCT06032572 -
Evaluation of the Safety and Effectiveness of the VRS100 System in PCI (ESSENCE)
|
N/A | |
Recruiting |
NCT05308719 -
Nasal Oxygen Therapy After Cardiac Surgery
|
N/A | |
Recruiting |
NCT04242134 -
Drug-coating Balloon Angioplasties for True Coronary Bifurcation Lesions
|
N/A | |
Completed |
NCT04556994 -
Phase 1 Cardiac Rehabilitation With and Without Lower Limb Paddling Effects in Post CABG Patients.
|
N/A | |
Recruiting |
NCT05846893 -
Drug-Coated Balloon vs. Drug-Eluting Stent for Clinical Outcomes in Patients With Large Coronary Artery Disease
|
N/A | |
Recruiting |
NCT06027788 -
CTSN Embolic Protection Trial
|
N/A | |
Recruiting |
NCT05023629 -
STunning After Balloon Occlusion
|
N/A | |
Completed |
NCT04941560 -
Assessing the Association Between Multi-dimension Facial Characteristics and Coronary Artery Diseases
|
||
Completed |
NCT04006288 -
Switching From DAPT to Dual Pathway Inhibition With Low-dose Rivaroxaban in Adjunct to Aspirin in Patients With Coronary Artery Disease
|
Phase 4 | |
Completed |
NCT01860274 -
Meshed Vein Graft Patency Trial - VEST
|
N/A | |
Recruiting |
NCT06174090 -
The Effect of Video Education on Pain, Anxiety and Knowledge Levels of Coronary Bypass Graft Surgery Patients
|
N/A | |
Completed |
NCT03968809 -
Role of Cardioflux in Predicting Coronary Artery Disease (CAD) Outcomes
|
||
Terminated |
NCT03959072 -
Cardiac Cath Lab Staff Radiation Exposure
|
||
Recruiting |
NCT04566497 -
Assessment of Adverse Outcome in Asymptomatic Patients With Prior Coronary Revascularization Who Have a Systematic Stress Testing Strategy Or a Non-testing Strategy During Long-term Follow-up.
|
N/A | |
Recruiting |
NCT05065073 -
Iso-Osmolar vs. Low-Osmolar Contrast Agents for Optical Coherence Tomography
|
Phase 4 | |
Completed |
NCT05096442 -
Compare the Safety and Efficacy of Genoss® DCB and SeQuent® Please NEO in Korean Patients With Coronary De Novo Lesions
|
N/A |