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Predictive Value of the Peripheral Perfusion Index for Pain Response in Critically Ill Patients with Consciousness Disorders

Predictive Value of the Peripheral Perfusion Index for Pain Response in Critically Ill Patients with Consciousness Disorders

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500112266
Enrollment
Unknown
Registered
2025-11-12
Start date
2025-12-01
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

None

Interventions

Observation group:None

Sponsors

Zhongshan People’s Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Voluntary signing of the informed consent form; 2. Age >= 18; 3. Expected mechanical ventilation duration >= 24 hours; 4. Patients with consciousness disorders (GCS <= 12 or RASS <= -3).

Exclusion criteria

Exclusion criteria: 1. Surgical patients 2. Peripheral vascular disease (upper extremity atherosclerosis, Raynaud's phenomenon, thromboangiitis obliterans, previous upper extremity vascular trauma or surgery, or wrist-brachial index WBI1.3) 3. Spinal cord injury 4. Brainstem/thalamic stroke 5. Severe peripheral neuropathy and disease 6. Brachial plexus injury 7. Guillain-barre syndrome 8. Use neuromuscular blocking agents 9. Multiple sclerosis, amyotrophic lateral sclerosis 10. Severe liver failure (Child-Pugh class C) 11. Severe arrhythmias (atrial fibrillation, frequent premature ventricular contractions) 12. Severe edema of the upper limbs 13. Core temperature 39 ° C 14. Burn or trauma precludes finger PPI monitoring 15. Fingertip capillary filling time >=3s 16. Near death 17. Use of high doses of vasoactive drugs (one of these: norepinephrine >=0.3µg/kg/min or equivalent, dopamine >=15µg/kg/min or epinephrine >=0.1µg/kg/min, vasoactive drug index (VIS) >=30); 18. Bispectral index (BIS) < 20, or with any one of the "supraorbital notch press/sternal press" standardized stimulus responsiveness screens were excluded: Patients with no behavioral response (?CPOT=0) or no physiological response (?HR<5 or ?MAP<5 MMHG) to noxious stimuli, or no neurophysiological response (?BIS <5); 19. According to the investigator's judgment, he was not suitable to participate in the study.

Design outcomes

Primary

MeasureTime frame
?PPI%;?COPT;Analysis of the Specific Response Pattern of PPI to Noxious Stimuli;Correlation analysis of ?PPI% with ?CPOT and ?BIS;

Secondary

MeasureTime frame
?HR??ABP??BIS;Comparison of pain recognition performance with different parameters;Analysis of the stratified effect of consciousness level on the predictive efficacy of PPI;

Countries

China

Contacts

Public ContactLizhen Zhu

Zhongshan People’s Hospital(Affiliated Zhongshan Hospital of Sun Yat-sen University)

18807603472@139.com+86 760 89880094

Outcome results

None listed

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