Sponsor study identifier
interventional
131
1 country
2
Study Start
May 21, 2024
Actual (reported)Primary Completion
December 21, 2025
Actual (reported)Study Completion
December 21, 2025
Actual (reported)The purpose of the study is to compare the effectiveness of two different methods of administering adenosine for the treatment of stable supraventricular tachycardia (SVT).
Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.
December 21, 2025
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Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.
May 21, 2024
Actual (reported)December 21, 2025
Actual (reported)December 21, 2025
Actual (reported)February 6, 2026
Actual (reported)April 28, 2026
Actual (reported)First-dose successful termination of PSVT
Proportion of participants with conversion from paroxysmal supraventricular tachycardia to sinus rhythm after the first dose of adenosine.
Within 2 minutes after administration of the first dose of adenosine.
Total administered dose of adenosine.
From administration of the first dose until successful termination of PSVT or up to 10 minutes, whichever occurs first.
Simplified method, containing both 6 mg of adenosine and 18 mL NS. If SVT termination failed: Second dose of adenosine with SS containing both 12 mg of adenosine and 18 mL NS. A total of three doses could be provided to each patient
One Syringe containing 6 mg of adenosine + one syringe containing 20 mL NS aided with a stopcock. If SVT termination failed: Second dose of adenosine (12 mg) + one syringe containing 20 mL NS. A total of three doses could be provided to each
Shahid Mohammadi Hospital
Bandar Abbas, Hormozgan, Iran
Shahid Mohammadi Hospital
Bandar Abbas, Iran
131 participants (actual enrollment reported by the registry).
First Submitted
February 6, 2026
First Posted
April 28, 2026
Study Start
May 21, 2024
Actual (reported)Propafenone Versus Amiodarone in Septic Shock
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Primary Completion
December 21, 2025
Actual (reported)Study Completion
December 21, 2025
Actual (reported)Last Updated
April 28, 2026
Record last verified: 2026-04
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Source: ClinicalTrials.gov.
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