[Nasal-cardiac reflex].
Stanisław Betlejewski, Andrzej Betlejewski, Danuta Burduk...
https://pubmed.ncbi.nlm.nih.gov/14994602/Actively Recruiting
Led by Marmara University Pendik Training and Research Hospital · Updated on 2026-06-01
60
Participants Needed
1
Research Sites
4 weeks
Total Duration
Researchers are evaluating treatments for supraventricular tachycardia SVT, a common heart rhythm disorder that causes a rapid heartbeat. The study compares a nasal swab technique with the modified Valsalva maneuver, the current best non-drug treatment, to see which better restores normal heart rhythm within one minute. This trial is conducted in two phases a pilot phase to test feasibility and gather data, followed by a main phase to finalize participant numbers based on pilot results. Participants are randomly assigned to one of two groups. One group receives a standard nasopharyngeal swab inserted through the nostril and held for 10 seconds while monitored. The other group performs the modified Valsalva maneuver, involving a forced expiration into a syringe followed by rapid repositioning and leg elevation. If the assigned method fails, intravenous adenosine is given as rescue therapy. The study is open-label for patients and care providers but has blinded outcome assessment and statistical analysis. During the study, participants are continuously monitored with heart rhythm, oxygen levels, and blood pressure checks. Researchers assess whether normal heart rhythm is restored within one minute and also measure outcomes at 3 and 5 minutes, patient discomfort, satisfaction, and recurrence of SVT at 24 hours and 30 days. Safety is closely monitored, and participants are followed up for 30 days to observe any adverse events or recurrence.
CONDITIONS
NASVAL-SVT: Nasal Swab Versus Modified Valsalva for Supraventricular Tachycardia
E
Emir Ünal
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Marmara University Pendik Training and Research Hospital
Lead Sponsor
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Single session lasting approximately 30 seconds to 1 minute
Participants receive one of two treatment procedures to terminate supraventricular tachycardia: either a nasal swab insertion held for 10 seconds or a modified Valsalva maneuver involving forced expiration followed by repositioning and leg elevation. Rescue therapy with intravenous adenosine is provided if the initial procedure fails.
1 treatment visit (in-person)
Duration - Up to 30 days after treatment
Participants are monitored for adverse events and treatment outcomes including heart rhythm conversion and recurrence of supraventricular tachycardia up to 30 days after the procedure.
Follow-up assessments at 24 hours and 30 days post-procedure
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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Lead Sponsor