Blood thinner trombix under Real-World review for heart rhythm disorder
NCT ID NCT06184204
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This completed study in Algeria followed 398 adults with atrial fibrillation who were taking the blood thinner Trombix (Rivaroxaban). The goal was to see how safe and effective the drug is in everyday medical practice, and how it affects quality of life. Researchers tracked serious bleeding events and other side effects.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Rivaroxaban (brand name Trombix), a blood thinner
- What this could lead to
- If results are positive, this could confirm that Trombix is a safe and effective option for managing atrial fibrillation in real-world settings in Algeria.
- What could go wrong
- This is an observational study, not a controlled trial, so it cannot prove cause and effect. Results may not apply to other populations or settings.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
-
398 people
The number who actually took part.
- Started
-
Dec 2023
- Finished
-
Jun 2025
- Lead sponsor
-
A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
The subjects in the study were enrolled from different centers (public and private sectors) across different regions in the country; East, Center and West of Algeria.
- Ages
-
19 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patient, male or female, aged ≥ 19 years. * Patient with a diagnosis of atrial fibrillation who requires treatment with Trombix® or switch of Anti-Vitamin K treatment toTrombix® (patient not balanced with current treatment or wishing to change treatment with better manageability). * Patient being able to provide free and informed written consent before the study. Exclusion Criteria: * Hypersensitivity to the active ingredient or to one of the excipients indicated in the Summary of Product Characteristics of Trombix® * Clinically significant progressive bleeding. * Injury or illness, if considered to be at significant risk of major bleeding. This may include: current or recent gastrointestinal ulceration, presence of malignant tumors with a high risk of bleeding, recent brain, spinal or ophthalmic surgery, recent intracranial hemorrhage, known or suspected esophageal varices, arteriovenous malformations, vascular aneurysms or major intra-spinal or intracerebral vascular anomalies. * Concomitant treatment with any other anticoagulant, for example, unfractionated heparin (UFH), low molecular weight heparins (enoxaparin, dalteparin, etc.), heparin derivatives (fondaparinux, etc.), oral anticoagulants (warfarin, dabigatran exilate, apixaban, etc.) except in specific circumstances of switching from anticoagulant treatment or in the case of administration of UFH at doses necessary to maintain the permeability of a central venous or arterial catheter. * Liver injury associated with coagulopathy and clinically significant bleeding risk, including cirrhotic patients with Child Pugh score class B or C. * Pregnancy and breast feeding
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Atrial fibrillation are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
AOUICHE private healthcare
Constantine, Algeria
-
Ali Lahmar private healthcare
Oran, Algeria
-
BEDAI private healthcare
Annaba, Algeria
-
Berboucha
Annaba, Algeria
-
Boudjelal private healthcare
Batna City, Algeria
-
Boumaaza Private healthcare
Algiers, Algeria
-
CHU Mustapha
Algiers, Algeria
-
CHU Oran
Oran, Algeria
-
EID private healthcare
Oran, Algeria
-
EPH Tipaza
Tipasa, Algeria
-
Fernane private healthcare
Tizi Ouzou, Algeria
-
HAMDI private healthcare
Constantine, Algeria
-
KHAITER Private healthcare
Blida, Algeria
-
Mouffok private healthcare
M'Sila, Algeria
-
NASSOUR private healthcare
Tlemcen, Algeria
-
OKBI Private healthcare
Biskra, Algeria
-
Sebbagh Private Healthcare
Sidi Bel Abbes, Algeria
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Heart hole or stroke trigger? global registry tracks who gets closure and what happens next
- Two ways to quiet a racing heart: trial pits hybrid ablation against standard catheter treatment
- Stroke's hidden heart rhythm clue under investigation
- Suture device may get heart patients walking sooner after leg vein procedures
- Two ways to catch a hidden heart rhythm after stroke
- Can an implanted heart monitor catch hidden irregular heartbeats after stroke?