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The comparison of changes using perfusion index before and after SGB on CRPS patients and non CRPS patients

The comparison of changes using perfusion index before and after SGB on CRPS patients and non CRPS patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0004278
Enrollment
20
Registered
2019-09-05
Start date
2019-10-01
Completion date
Unknown
Last updated
2019-10-07

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

Conditions

None listed

Interventions

None listed

Sponsors

Inha University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who taken stellate ganglion block due to head and upper pains Patients aged 19-80 years Patients and caregivers agreed to this study patients under the American society of anesthesiologists classification ?

Exclusion criteria

Exclusion criteria: Patients with severe coagulation disorders Severe lung disease patients Patients who have allergic reactions to the test drug Patients whose written consent is difficult to communicate due to lack of communication Pregnant women By definition of clinical trial committee of medical institutions where clinical trials are conducted, vulnerable subjects

Design outcomes

Primary

MeasureTime frame
Changes of perfusion index after stellate ganglion block—

Secondary

MeasureTime frame
Changes in skin temperature , pain intensity and vital signs after stellate ganglion block—

Countries

Korea, Republic of

Contacts

Public ContactKIM

Inha University Hospital

friskygirl@naver.com+82-32-890-3963

Outcome results

None listed

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