Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04332952
Other study ID # Cardiologia-002
Secondary ID
Status Completed
Phase
First received
Last updated
Start date August 1, 2017
Est. completion date December 31, 2017

Study information

Verified date April 2020
Source Hospital Beneficencia Espanola de Puebla
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The glycocalyx is a component of the vascular endothelium that currently plays a relevant role in the modified Starling theory.

The manipulation of the heart during cardiac surgery stimulates the release of the natriuretic atrial peptide, which causes endothelial wear in patients undergoing extracorporeal circulation. Dilation of the atrium produces natriuretic atrial peptide, which reduces plasma volume by increasing renal excretion and vascular permeability. The atrial peptide degrades the surface of the coronary endothelium, causing loss of the side cam protein nucleus. This study investigates the relationship between clamping time in cardiac surgery and the clearance of endothelial inflammation markers.


Recruitment information / eligibility

Status Completed
Enrollment 21
Est. completion date December 31, 2017
Est. primary completion date October 1, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Over 18 years of age

- Patients who underwent cardiac surgery for a single valve change or replacement

Exclusion Criteria:

- Stage 3 renal failure patients

- Patients with a previous diagnosis of hematological malignancy

- Patients undergoing pulmonary valve change surgery.

- Patients undergoing Bentall and Bono surgery.

- Patients Undergoing Coronary Artery Bypass Surgery

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Mexico Hospital Beneficencia Española de Puebla Puebla

Sponsors (2)

Lead Sponsor Collaborator
Miguel Ayala León Instituto Nacional de Cardiologia Ignacio Chavez

Country where clinical trial is conducted

Mexico, 

Outcome

Type Measure Description Time frame Safety issue
Primary Extracorporeal circulation time Duration of Extracorporeal Circulation in minutes 2 hours
Primary Aortic clamping time Duration of aortic clamping time in minutes 2 hours
Primary Hyaluronic acid levels in blood before surgery Quantity of hyaluronic acid in blood before surgery 30 minutes
Primary Hyaluronic acid levels in blood after surgery Quantity of hyaluronic acid in blood after surgery 30 minutes
Primary Hyaluronic acid levels in urine before surgery Quantity of hyaluronic acid in urine before surgery 30 minutes
Primary Hyaluronic acid levels in urine after surgery Quantity of hyaluronic acid in urine before surgery 30 minutes
Primary Sydecan -1 levels in blood before surgery Quantity of Sydecan -1 in blood before surgery 30 minutes
Primary Sydecan -1 levels in blood after surgery Quantity of Sydecan -1 in blood after surgery 30 minutes
Primary Sydecan -1 levels in urine before surgery Quantity of Sydecan -1 in urine before surgery 30 minutes
Primary Sydecan -1 levels in urine after surgery Quantity of Sydecan -1 in urine after surgery 30 minutes
See also
  Status Clinical Trial Phase
Recruiting NCT05053893 - Roxadustat Combined With Sacubitril Valsartan Sodium Tablets in the Treatment of Cardiorenal Anemia Syndrome N/A
Recruiting NCT03176862 - Left Ventricular Fibrosis in Chronic Kidney Disease N/A
Recruiting NCT04170855 - Kidney Sodium Content in Cardiorenal Patients N/A
Not yet recruiting NCT05079724 - Acute Kidney Injury After Cardiac Surgery
Withdrawn NCT02085668 - Renal Denervation in Patients With Chronic Heart Failure N/A
Terminated NCT02772146 - A Clinical Study of the Safety and Efficacy of a Wearable Device (CLS UF) That Delivers Continuous Administration of Glucose to Recirculated Peritoneal Dialysis Fluid for the Purpose of Ultrafiltration in Patients With Congestive Heart Failure N/A
Recruiting NCT02846337 - Ultrafiltration Versus Medical Therapies in the Management of the Cardio Renal Syndrome N/A
Active, not recruiting NCT02502981 - Comparing the Effects of Spironolactone With Chlortalidone on LV Mass in Patients With CKD Phase 4
Recruiting NCT04947670 - A Prospective, Multicenter, Randomized, Blinded, Sham-controlled, Feasibility Study of Renal Denervation in Patients With Chronic Heart Failure N/A
Not yet recruiting NCT05368766 - Predictive Value of Venous Excess Ultrasound Score in Management of Cardiorenal Patients
Withdrawn NCT02959281 - Bioimpedance and Hand-held Echocardiographay for Clinical Decision-making in Treatment of Cardio-renal Syndrome Type I N/A
Completed NCT04407936 - Risk Factors and Prognosis of Adverse Cardiovascular and Kidney Events After Coronary Intervention
Completed NCT05050877 - Risk Factors and Prognosis of Adverse Cardiovascular and Kidney Events After Coronary Intervention II
Recruiting NCT03628443 - Cardiorenal Risk Stratification Pilot Study
Recruiting NCT02343393 - Nitrates In Combination With Hydralazine in cardiorEnal Syndrome (NICHE) Study Phase 3
Completed NCT02664246 - Contrast-induced Nephropathy: Incidence,Risk Factors,Effective Prevention and Management Method N/A
Completed NCT03219996 - Risk Factors for Predictors of In-hospital Death in Acute Fulminant Myocarditis N/A
Completed NCT04145635 - The Aortix CRS Pilot Study N/A
Completed NCT02405377 - Central Venous Pressure Guided Hydration Prevention for Contrast-Induced Nephropathy N/A
Recruiting NCT05677100 - Diuretics Alone vs. Aortix Endovascular Device for Acute Heart Failure N/A