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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03249545
Other study ID # ozcan02
Secondary ID
Status Recruiting
Phase N/A
First received August 6, 2017
Last updated August 9, 2017
Start date July 1, 2017
Est. completion date March 1, 2019

Study information

Verified date August 2017
Source Yuksek Ihtisas Hospital
Contact Firat Ozcan, Ass. Prof, MD
Phone +905327854000
Email drfozcan@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Premature Ventricular Complex (PVC) ablation is performed in certain indications. Generally acutely abolition of PVC at the time of ablation accepted as successful ablation. However in some patients this effect occurs lately. In this study investigators sought late effect of ablation


Description:

On tissue level ablation lesion deepens and enlarges by time following the procedure. Based on this, investigators aimed to seek patients who has no acute success but late success. This phenomenon occurs in some patients. Investigators investigate the characteristics of those patients on both procedural and clinical aspects. Investigators enroll patients applied during prespecified dates


Recruitment information / eligibility

Status Recruiting
Enrollment 30
Est. completion date March 1, 2019
Est. primary completion date December 31, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

Patients who had both of the criteria below

- Presence of premature ventricular complex requiring ablation

- Successfully abolition of premature ventricular complex hours after the procedure

Exclusion Criteria:

Patients who had either of below mentioned criteria

- Abolition of premature ventricular complex during the procedure

- Unsuccessful procedure

Study Design


Locations

Country Name City State
Turkey Turkiye Yuksek Ihtisas Training and Research Hospital Ankara

Sponsors (1)

Lead Sponsor Collaborator
Yuksek Ihtisas Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Success Continuation of ablation on the long term 3 months
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