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A TRIAL COMPARING EFFECTIVENESS OF TWO MANEUVERS FOR TREATMENT OF SUDDEN AND ABNORMALLY INCREASED HEART RATE

Not Applicable
Conditions
Health Condition 1: I471- Supraventricular tachycardia
Registration Number
CTRI/2021/01/030684
Lead Sponsor
Department of Emergency Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.Patients/Legally Authorized Representative(LAR) providing Informed consent

2. Diagnosis of supraventricular tachycardia (SVT; regular, narrow complex tachycardia with QRS duration <0.12 s on ECG with absent or overt p wave)

Exclusion Criteria

I. Unable or unwilling to give informed consent

II. Unstable condition (systolic blood pressure (BP) <90 mm Hg or any indication for immediate drug or direct current cardioversion)

III. Atrial fibrillation/atrial flutter/sinus tachycardia/MAT on ECG

IV. Systemic hypoperfusion

i. Altered mentation

ii. Chest pain (due to coronary ischemia)

iii. Dyspnea (due to pulmonary edema)

V. Severe hypertension (systolic BP >220 mm Hg or diastolic BP >120 mm Hg)

VI. Any contraindication to or inability to performing a Valsalva maneuver

VII. Contraindication or inability to lay flat and have legs lifted (or any reason identified by the patient as to why this maneuver would cause discomfort or pain)

VIII. Pregnancy

IX. Myocardial Infarction( <3 months)

X. Known case of glaucoma or retinopathy

XI. Previous inclusion in the study

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Cardioversion in Patients with supraventricular tachycardia(achievement of normal sinus rhythm on electrocardiography after standard/modified valsalva maneuver)Timepoint: 1 minute
Secondary Outcome Measures
NameTimeMethod
â??To compare sustained success rates at the third and fifth minute of application of the maneuver in each arm <br/ ><br>â?? Failure to revert SVT to a sinus rhythm, followed by: <br/ ><br>i) repeated attempts at Standard or Modified Valsalva Maneuver <br/ ><br>ii) pharmacological intervention; or <br/ ><br>iii) direct current countershock therapies. <br/ ><br>â?? To compare frequency and severity of adverse events resulting from application of maneuversTimepoint: 3, 5 minutes
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