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Which heparin method works best during heart ablation?
NCT ID NCT07361081
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at two methods of giving the blood thinner heparin during a procedure called atrial fibrillation ablation. The goal is to see which method keeps the blood's clotting time in a safe range more often. Researchers reviewed records of 300 patients who had the procedure between 2018 and 2020. The findings could help reduce complications like stroke or bleeding.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- heparin
- What this could lead to
- If successful, this could point to a safer, more consistent way to give heparin during heart procedures, potentially reducing stroke and bleeding risks.
- What could go wrong
- This is a small, single-center retrospective study, not a large randomized trial. Results may not apply to all patients or hospitals.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
-
300 people
The number who actually took part.
- Started
-
Sep 2022
- Expected to finish
-
Dec 2028
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
This is a single-center and retrospective cohort study. The study will enroll patients above 20 years old and received RF ablation for AF from 2018 to the end of 2020. The baseline characteristics of the patients will be obtained from the electronic medical records, including age, sex, body weight, body height, risk factors of stroke, cardiac echo, laboratory data, and medications. Three experienced attending physicians are involved in the study. Two used the prespecified continuous infusion protocol to adjust heparin doses.
- Ages
-
20 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Above 20 years old 2. Received RF ablation for AF from 2018 to the end of 2020 Exclusion Criteria: \-
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
National Taiwan University Hospital,
Taipei, 100, Taiwan
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Other studies related to the condition(s) this trial covers.
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