- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00005195
Catheter Ablation Registry
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
BACKGROUND:
Cardiac tachyarrhythmias that are refractory to either conventional or experimental antiarrhythmic therapy, antitachycardia pacemakers, or both, may result in serious symptoms or death. Catheter ablation has been developed as a nonpharmacologic, closed-chest alternative for the management of these patients. The technique was first applied to man in 1981 and reported by both Scheinman et al and Gallagher et al in 1982. Hartzler reported the first catheter ablation procedure for the treatment of ventricular tachycardia in 1983. In that same year, Weber reported the first use of catheter ablation of an accessory atrioventricular pathway. The standard method of energy delivery for closed-chest catheter ablation attempts involved direct current delivered using a defibrillator, but beginning in 1985, radiofrequency energy was employed in man. This promised to revolutionize the field of catheter ablation, because it offered the hope of more precise destruction of tissue, avoided the need for general anesthesia and significantly lowered complication rates, since it did not involve the levels of energy used in direct current attempts.
The Catheter Ablation Registry (CAR) evolved from a pilot study, the Percutaneous Cardiac Mapping and Ablation Registry (PCMAR) formed in 1983. There were scientific limitations in this voluntary registry. Further prospective studies were needed to better define this procedure, and a multicenter international prospective cohort study was designed to allow a rapid assessment of ablation's dangers and potential usefulness. Results from the study were used to guide physicians as to which patients would and would not benefit from these new procedures.
DESIGN NARRATIVE:
Data were collected prospectively from sixteen clinical centers in the United States and Europe on attempted catheter ablation of the atrioventricular junction, accessory atrioventricular pathways and ventricular tachycardia. Each of the three ablation techniques was studied as a separate subset and the two methods of energy delivery, direct current or radiofrequency energy, were compared within each subset. A standardized protocol was used for direct current ablation and the results of a variety of protocols for the other two procedures and for radiofrequency energy were observed. Patients were evaluated quarterly in the first post-procedure year, and biannually for the subsequent duration of the study. Statistical analyses were performed to determine the distribution of specific patient characteristics such as age, sex, clinical status, underlying heart disease, and a variety of procedural categories including energy level, mapping data, and catheter position. A determination was made of the frequency of successful outcomes including cessation of arrhythmias, production of third degree atrioventricular block, and disappearance of symptoms and of adverse effects, including procedure-related complications and death.
The study completion date listed in this record was obtained from the "End Date" entered in the Protocol Registration and Results System (PRS) record.
Study Type
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Study Plan
How is the study designed?
Collaborators and Investigators
Publications and helpful links
General Publications
- Fisher JD, Scavin GM, Roth JA, Ferrick KJ, Kim SG, Johnston DR, Williams HR, Frame R. Direct current shock ablation: quantitative assessment of proarrhythmic effects. Pacing Clin Electrophysiol. 1991 Dec;14(12):2154-66. doi: 10.1111/j.1540-8159.1991.tb06486.x.
- Evans GT Jr, Scheinman MM, Bardy G, Borggrefe M, Brugada P, Fisher J, Fontaine G, Huang SK, Huang WH, Josephson M, et al. Predictors of in-hospital mortality after DC catheter ablation of atrioventricular junction. Results of a prospective, international, multicenter study. Circulation. 1991 Nov;84(5):1924-37. doi: 10.1161/01.cir.84.5.1924.
Study record dates
Study Major Dates
Study Start
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1074
- R01HL035077 (U.S. NIH Grant/Contract)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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