Actively Recruiting

Phase 3
Age: 18Years - 70Years
All Genders
NCT06717685

Efficacy of Adenosine as Compared to Verapamil in Paroxysmal Supraventricular Tachycardia (pSVT) Patients

Led by Rashid Latif Medical College · Updated on 2024-12-13

210

Participants Needed

1

Research Sites

14 weeks

Total Duration

On this page

Sponsors

R

Rashid Latif Medical College

Lead Sponsor

P

Punjab Institute of Cardology

Collaborating Sponsor

AI-Summary

What this Trial Is About

Supraventricular tachycardia (SVT) is a term widely used to describe tachycardial dysrhythmias, paroxysmal SVT (PSVT) is a narrow term including only AV nodal re-entrant tachycardia (AVNRT) and atrioventricular re-entrant tachycardia (AVRT), both of which can cause discomfort and, in some cases, life-threatening symptoms. Usually Carotid sinus massage is done to lower the pulse rate and after the standard time specific verapamil dose is administered. In this study after carotid sinus massage Conventional Valsalva or modified Valsalva maneuver will be randomly applied. In case, the normal sinus rhythm (NSR) is not achieved then verapamil of or adenosine dose will be administered to the patients after after taking the consent.

CONDITIONS

Official Title

Efficacy of Adenosine as Compared to Verapamil in Paroxysmal Supraventricular Tachycardia (pSVT) Patients

Who Can Participate

Age: 18Years - 70Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Stable supraventricular tachycardia (SVT) not requiring cardioversion, fully conscious, and systolic blood pressure above 90 mmHg
  • Alert and able to provide informed consent
  • Able to lie flat comfortably with non-painful legs during passive leg raising
Not Eligible

You will not qualify if you...

  • Unstable supraventricular tachycardia with symptoms such as semi-consciousness, drowsiness, breathlessness, or systolic blood pressure below 90 mmHg
  • Unable to give consent
  • Orthopnea causing inability to lie flat
  • Presence of atrial fibrillation or atrial flutter
  • Recent myocardial infarction within the last 7 days
  • Ongoing ischemia indicated by chest pain or ECG changes
  • Aortic stenosis
  • Pregnancy in any trimester

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Punjab Institute of Cardiology

Lahore, Punjab Province, Pakistan

Actively Recruiting

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Research Team

A

Abdul Manan Shahid, FCPS

CONTACT

A

Arslan Saleem Chughtai, M.Phil.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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