Flexible wearable microfluidic intelligent sensing system for non-invasive continuous monitoring of key biochemical indicators mornitoring during perioperative period

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2400080916

Enrollment

Unknown

Registered

2024-02-18

Start date

2024-02-18

Completion date

Unknown

Last updated

2024-02-19

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

Conditions

internal environment disturbance

Interventions

observation group :None

Eligibility

Sex/Gender

All

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: ? 18-65 years old; ? Estimated operation time =3 h; ? Invasive arterial catheterization and intraoperative blood gas analysis are required; ? ASA classification I-III.

Exclusion criteria

Exclusion criteria: ? The patient could not undergo invasive arterial puncture; ? Due to medical safety or patient comfort considerations, the doctor in charge believes that it is not appropriate to take blood repeatedly; ? The patient is allergic to hydrogels/plastic films; ? Patients wear cardiac pacemakers or other conditions that are not suitable for electrical stimulation to collect sweat; ? Patients refused to participate.

Design outcomes

Primary

Measure	Time frame
Lactic acid value of sweat;Potassium ion value of sweat;Calcium ion value of sweat;	—

Secondary

Measure	Time frame
Lactic acid value of arterial blood;Potassium ion value of arterial blood;Calcium ion value of arterial blood;	—

Countries

China

Contacts

Public ContactZheng Hui

National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College

zhenghui@cicams.ac.cn+86 138 1151 6861

Outcome results

None listed

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