Application of dynamic glucose monitoring system in patients with acute respiratory failure

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2200061801

Enrollment

Unknown

Registered

2022-07-02

Start date

2022-07-10

Completion date

Unknown

Last updated

2023-04-03

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

Conditions

Acute respiratory failure

Interventions

Experimental group:Blood glucose was monitored using FGM

control group:Routine fingertip blood glucose monitoring method for monitoring intervention

Eligibility

Sex/Gender

All

Age

18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age > 18; 2. Diagnosis of acute respiratory failure or acute onset of chronic respiratory failure; 3. Informed and agreed to participate in the study; 4. Acute Physiology and Chronic health Status Scoring System (APACHE II) > 10/SOFA score > 10.

Exclusion criteria

Exclusion criteria: 1. Withdraw from the study; 2. Skin edema, injury or infection at the probe placement site; 3. Coagulation dysfunction such as severe platelet abnormalities; 4. Pregnancy or perinatal period.

Design outcomes

Primary

Measure	Time frame
Mean blood glucose fluctuation range;Time within target range;Standard deviation of 24h blood glucose;Standard deviation of 24h blood glucose;Hypoglycemic index;Standard deviation of 24h blood glucose;	—

Secondary

Measure	Time frame
Accuracy index of glucose data;Use safety and stability indicators;	—

Countries

China

Contacts

Public ContactZhang Jianna

Emergency department of West China Hospital of Sichuan University

9318696@qq.com+86 18980606994

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026