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A Randomized Controlled Trial of Sertraline in Paroxysmal Arterial Hypertension

A Randomized Controlled Trial of Sertraline in Paroxysmal Arterial Hypertension (ATRAX Trial)

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02641652
Acronym
ATRAX
Enrollment
136
Registered
2015-12-29
Start date
2017-11-30
Completion date
2018-12-31
Last updated
2017-09-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertension

Keywords

paroxysmal hypertension, pseudopheochromocytoma

Brief summary

There is currently no established treatment for paroxysmal hypertension, but selective serotonin reuptake inhibitors showed good effect in previous reports. This double-blind, placebo controlled, prospective multicenter clinical trial will assess the efficacy of sertraline on cessation or reduction of symptoms of paroxysmal arterial hypertension. 136 patients with documented hypertensive paroxysms with abrupt elevations of blood pressure and distressful physical symptoms will be randomized in a 1:1 ratio to receive sertraline, 50 mg daily, or matching placebo as an add-on to their chronic medication. Effect of the treatment on patient symptoms, office and ambulatory blood pressure and side effects will be evaluated after 3 months. If proven effective, sertraline might become a standard treatment for this condition.

Interventions

DRUGSertraline

25 mg once daily for first 7 days, then 50 mg once daily for the rest of the trial

DRUGPlacebo

1/2 tablet once daily for first 7 days, then 1 tablet once daily for the rest of the trial

Sponsors

Brno University Hospital
CollaboratorOTHER
St. Anne
CollaboratorUNKNOWN
University Hospital Ostrava
CollaboratorOTHER
Tomas Bata Hospital, Czech Republic
CollaboratorOTHER
Prerov Hospital
CollaboratorUNKNOWN
Valasske Mezirici Hospital
CollaboratorUNKNOWN
Thomayer University Hospital
CollaboratorOTHER
Vsetin Hospital
CollaboratorUNKNOWN
University Hospital Olomouc
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Study will enroll adult patients (age \>18 years) with hypertensive paroxysms during the past 6 months (preferably during the past 6 weeks) - abrupt elevations of systolic blood pressure (BP) ≥20% compared to previous measured systolic BP value before paroxysm, or ≥20% compared to mean systolic BP on 24-hour ambulatory blood pressure monitoring (ABPM), or ≥20% compared to measured office systolic BP, documented by a clinician or home blood pressure monitor, requiring physician or emergency room visit or the use of any rescue antihypertensive medication. Hypertensive paroxysms may be accompanied by abrupt onset of one or more distressful physical symptoms, such as headache, chest pain, dizziness, nausea, palpitations, flushing, and diaphoresis.

Exclusion criteria

Pregnancy or breastfeeding, hypersensitivity to sertraline (Zoloft®) or of the the components of this drug. Current use of sertraline or any other selective serotonin reuptake inhibitor (SSRI), mono-amin oxidase (MAO) inhibitors, selegiline, moclobemide, linezolide, pimozide. Current use of other serotoninergic drugs (eg. tryptofane, triptane and other 5-HT agonists), tramadol or dopamine antagonists (including antipsychotics).

Design outcomes

Primary

MeasureTime frame
difference in the rate of paroxysmal hypertension symptoms cessation between sertraline and placebo groups3 months of treatment
difference in the rate of paroxysmal hypertension symptoms reduction between sertraline and placebo groups3 months

Secondary

MeasureTime frame
difference in the fall of mean office and ambulatory systolic and diastolic blood pressure between groups3 months
side effects of the treatment3 months

Contacts

Primary ContactJan Vaclavik, MD. Ph.D. Assoc. Prof.
janvaclavik@yahoo.com+420588442682
Backup ContactIrena Opavska, Bc.
irena.opavska@fnol.cz+420588443716

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026