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Effect of Dexmedetomidine on Pacemaker Function Following Cardiac Surgery

Nationwide Children's Hospital logo

Nationwide Children's Hospital

Status

Withdrawn

Conditions

Congenital Heart Disease

Treatments

Drug: Dexmedetomidine

Study type

Observational

Funder types

Other

Identifiers

NCT02709200
IRB13-00127

Details and patient eligibility

About

This is a prospective study looking at the effects of dexmedetomidine on pacemaker function in patients who have surgery for congenital heart disease utilizing cardiopulmonary bypass (CBP). For the purpose of the study, no change in intraoperative care will be dictated. The use of dexmedetomidine will be left up to the discretion of the treating physicians. The study will involve only the collection of data regarding the amplitude required to capture and specific demographics and intraoperative features including cross clamp time, time on CPB, and vasoactive agents that were and are being administered. In addition to these data, it will be noted whether dexmedetomdine was used or not and whether it is being administered on arrival to the CTICU.

Sex

All

Ages

6+ months old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with temporary surface pacemaker leads following surgery for congenital heart disease.

Exclusion criteria

  • Patients with single ventricle anatomy
  • Patients receiving epinephrine
  • Infants less than 6 months of age

Trial design

0 participants in 2 patient groups

Dexmedetomidine
Description:
Patients that received dexmedetomidine during open heart surgery.
Treatment:
Drug: Dexmedetomidine
No dexmedetomidine
Description:
Patients that didn't receive dexmedetomidine during open heart surgery.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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