With real-world data to clinical evidence
With real-world data to clinical evidence
Clinical research needs real life data - SaniQ TRIAL transforms every day of study participation into valuable real world data and clinical evidence.
3 Challenges in clinical studies:
3 Challenges in clinical trials
Generate real-world data
Reduce the dropout rate
Communicate efficiently
... und wie SaniQ TRIAL Sie dabei unterstützt:
SaniQ TRIAL turns every day of study participation into valuable real-world data that you can track in real time via the SaniQ Dashboard.
Real-World-Daten
generieren
Generate real-world data
Kontinuierliche Daten
- Telemonitoring of vital signs
- Electronic questionnaires (PREMs & PROMs)
- Medication planner incl. intake times
Die Abbruchquote
reduzieren
Reduce the dropout rate
Bessere Compliance
- Patient app for the active involvement of test subjects
- Medication planner incl. reminder function in the app
- Convenient and secure communication via televisite & chat
Communicate efficiently
Communicate efficiently
Effiziente Therapiesteuerung
- Automated monitoring alarms
- Quick contact via chat & televisite
- Adjustment of the dosage in the medication planner
Smart solutions for efficient clinical trials
Smart solutions for efficient clinical trials
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Modules & functions
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Benefits for clinics
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|---|---|
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Telemonitoring (vital signs such as blood pressure, weight, FEV1, etc.)
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Continuous data collection for study endpoints, reduction of study cancellations through better compliance
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Workflow Manager
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Structured distribution of tasks between trial centre, CRO and investigators
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Intersectoral communication
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GDPR-compliant exchange between different stakeholders
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Patient app
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Active involvement of study participants in the course of the study and improvement of adherence
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Chat & Televisite
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Direct contact in the event of side effects, queries or protocol-relevant events
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EDC interfaces (CDISC, CDASH, etc.):
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Seamless integration into existing study management systems and electronic data capture systems
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- CE-approved Class I medical device
- GDPR-compliant data protection and ISO 27001-certified
- Standardised interfaces to your HIS (HL7, FHIR)
-
CE-approved
Class I medical device -
GDPR-compliant data protection
and certified according to ISO 27001 -
Standardised interfaces
to your HIS (HL7, FHIR)
Use case: Telementor COPD study
The Telementor COPD study, funded by the G-BA Innovation Fund, is using SaniQ TRIAL to investigate the benefits of telemedicine for patients with COPD.
Period: 2022-2025
Partner: Lungenclinic Großhansdorf, Astra Zeneca, University Medical Centre Schleswig-Holstein, University Medical Centre Hamburg-Eppendorg, and many more.
Number of participants in the study: 640
Content: The Telementor COPD study is a multicentre, randomised and controlled clinical trial funded by the G-BA Innovation Fund under Consortium management of the LungenClinic Großhansdorf. The aim of the study is to prevent exacerbations in COPD patients through digital prevention and home monitoring.
Link to the study website: https://www.telementor-copd.de/
As part of the study, various vital signs of the patients are monitored using SaniQ OS and connected sensors (telespirometer, smartwatch) and analysed by the study staff:
- Telemonitoring lung function (FEV1), heart and respiratory rate, blood-oxygen saturation and daily step count for continuous patient monitoring
- API connection to the hospital information system for automated and bidirectional transmission of patient-related data
- Patient app to actively involve patients in the care programme and to generate patient-reported outcomes
- The study personnel regularly Televisits with the connected patients through
ZDF reports on COPD study with SaniQ
ZDF has reported on the Telementor COPD study, in which our SaniQ OS telemonitoring platform was used to monitor COPD patients.
to the article
Medien berichten über Studien mit SaniQ
SaniQ has already been used profitably in numerous clinical studies and research projects:
09. Juni 2026
Springer Nature
coverCHILD: Kinder mit Long COVID besser versorgen
Forschende der Philipps-Universität Marburg haben mithilfe von SaniQ untersucht, wie Telemonitoring die Versorgung von Kindern mit Post-COVID-Syndrom verbessern kann.
05 March 2026
German Medical Journal
Through the jungle of guidelines with AI
The European consortium GUIDE-AI - coordinated by Charité Berlin - is developing AI-based assistants for doctors with the help of SaniQ OS.
19 Nov. 2025
ZDF media library
ZDF report on study with SaniQ
ZDF reported on the Telementor COPD study, in which SaniQ OS was used for the medical monitoring of COPD patients.
What researchers say about SaniQ TRIAL
Let's talk about your project idea!
Jonas Zimmer
-Project development-
Let's talk about your project idea!
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- Individual topic focus
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