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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03667235
Other study ID # 2017-01334; ch17Reuthebuch2
Secondary ID
Status Completed
Phase
First received
Last updated
Start date August 4, 2017
Est. completion date October 31, 2019

Study information

Verified date December 2019
Source University Hospital, Basel, Switzerland
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To compare mechanic and thermic stability of pericardium fixated either with 0.6% glutaraldehyde for 10 minutes or with 0.6% glutaraldehyde for 20 minutes


Description:

Autologous pericardium for aortic valve reconstruction is treated with 0.6% glutaraldehyde for 10 minutes to improve stability (OKAZI technique).

This study investigates whether treatment with 0.6% glutaraldehyde for 20 minutes improves mechanic and thermic stability of autologous pericardial tissue. Autologous pericardium remaining after aortic valve reconstruction surgery is used.

To investigate 10 versus 20 minutes treatment of removed original aortic valve tissue with glutaraldehyde as a reference.


Recruitment information / eligibility

Status Completed
Enrollment 6
Est. completion date October 31, 2019
Est. primary completion date October 31, 2019
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- patients undergoing aortic valve surgery with sufficient leftover tissues from the OZAKI procedure (excess of pericardium and calcified aortic valve leaflets)

Exclusion Criteria:

- denial of consent

- insufficient leftover tissues from the OZAKI procedure

- patients after thoracic radiation or surgery

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Treatment of human pericardium with glutaraldehyde in OZAKI procedure
10 versus 20 minutes treatment of human pericardium with 0.6% glutaraldehyde in OZAKI procedure
Treatment of human aortic valve tissue with glutaraldehyde
10 versus 20 minutes treatment of human aortic valve tissue with 0.6%glutaraldehyde

Locations

Country Name City State
Switzerland Herzchirurgie University Hospital Basel Basel

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Basel, Switzerland

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary mechanic stability tests to investigate uniaxial and cyclical tensile properties mechanical tests include the use of a universal test machine (MTS Bionix, Department of Bioengineering of Universitaetsspital Basel) for:
uniaxial ultimate tensile strength (UTS) test;
cyclical tensile stretching of the tissue in order to investigate its viscoelastic properties
4 days after surgery
Primary thermic stability by using constant force at linearly increasing temperature constant force at linearly increasing temperature: Thermal stability tests will be conducted on 20 x 4 mm stripes by the imposition of a constant load (approximately 1N) submerged in a saline-solution bath. The temperature of the bath will be increased at a rate of approximately 2.5-5 °C/min, and the sample cross-section will be measured by means of a high-resolution camera (Canon EOS, Japan) 4 days after surgery
Secondary histologic analysis of collagen fiber organization and quantification histologic analysis by Scanning Electrical Microscopy (SEM) and using Picrosirius staining to identify the types I and IV collagen 4 days after surgery
Secondary Pronase testing to analyse enzymatic degradation Pronase testing to analyse enzymatic degradation 4 days after surgery
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