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FGM in Allogeneic Hematopoietic Stem Cell Transplantation Recipients

Safety of Flash Sensor-based Glucose Monitoring in Allogeneic Hematopoietic Stem Cell Transplantation Recipients - FGM-SCT P1 Study

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs052180059
Enrollment
6
Registered
2019-02-14
Start date
2017-11-30
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Patients who will receive hematopoietic stem cell transplantation

Interventions

Flash Sensor-based monitoring for 28days

Sponsors

MINAMI Hironobu
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1)Patients who are at least 20 and under 70 years of age (2)Patients who will undergo allogeneic hematopoietic stem cell transplantation (3)Patients who sign a written informed consent (4)Patients who have never used FreeStyle LibrePro

Exclusion criteria

Exclusion criteria: (1)Patients who will undergo HLA haplo-identical stem cell transplantation (2)Patients who need to perform X-ray or CT scan more than once a week (3)Patients who have infection on their upper arms for sensor sites (4)Patients who contact dermatitis (5)Patients who cannot use alcohol and chlorhexidine gluconate for sterilization (6)Patients who have implanted medical devices (7)Patients judged inappropriate perticipants for this study by their attending doctors

Design outcomes

Primary

MeasureTime frame
(1)Severe bleeding of the sensor site (2)Requirement of antibiotics due to the infection of the sensor site

Secondary

MeasureTime frame
(1)Correlation with the value of blood glucose and interstitial fluid glucose (2)The times of the sensor exchanges (3)Insertion site symptoms (4)Relationship between bleeding (onset and degree) and patients characteristics

Contacts

Public ContactKimikazu YAKUSHIJIN

Kobe University Hospital

kyakushi@med.kobe-u.ac.jp+81-78-382-5820

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026