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NCT02697448Completed

Comparison of Propofol and Sevoflurane as a Primary Anesthetic for Cardiac Ablation of Atrial Fibrillation.

Source: ClinicalTrials.gov · Last updated 20 Aug 2024

Brief summary (registry, in English)

Comparison of propofol and sevoflurane as a primary anesthetic for cardiac ablation of atrial fibrillation

Status (registry)
Completed
Study type
Interventional
Enrollment
135 (actual)
First submitted
29 Feb 2016
Start date
8 Jun 2016
Primary completion date
30 Jun 2023
Lead sponsor
Medical University of South Carolina
NCT number
NCT02697448

What you commit to

  • Study type: Interventional
  • Participants enrolled: 135
  • From 8 Jun 2016 to the primary completion date, 30 Jun 2023
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • none

Who the study is looking for

  • have paroxysmal atrial fibrillation
  • undergoing their first ablation.

Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Medical University of South Carolina
Coordinator of this site? Confirm its status
CharlestonUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.