NCT05723419

Brief Summary

The primary endpoint of this study was to identify that Perfusion index (PI) has any predictive value for the treatment outcome of cervical radiculopathy

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
70

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Feb 2023

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 3, 2023

Completed
7 days until next milestone

First Posted

Study publicly available on registry

February 10, 2023

Completed
3 days until next milestone

Study Start

First participant enrolled

February 13, 2023

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 30, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 30, 2023

Completed
Last Updated

February 15, 2023

Status Verified

February 1, 2023

Enrollment Period

10 months

First QC Date

February 3, 2023

Last Update Submit

February 13, 2023

Conditions

Outcome Measures

Primary Outcomes (5)

  • Perfusion index changes among 4 time periods

    Perfusion index changes among 4 time periods

    baseline, 10 minutes, 20 minutes, 30 minutes after axillary block

  • Number of patients showing numerical rating scale reduction more than 50%

    Number of patients showing numerical rating scale reduction more than 50%

    1 month after axillary block

  • Number of patients showing numerical rating scale reduction less than 50%

    Number of patients showing numerical rating scale reduction less than 50%

    1 month after axillary block

  • Number of patients showing no reduction in numerical rating scale

    Number of patients showing no reduction in numerical rating scale

    1 month after axillary block

  • Neck disability index changes between 2 time periods

    Neck disability index changes between 2 time periods

    baseline, 1 month after axillary block

Interventions

ultrasoud guided axillary block

Eligibility Criteria

Age20 Years - 80 Years
Sexall
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Patients who visit the pain clinic

You may qualify if:

  • Cervical foraminal stenosis
  • Cervical central stenosis
  • Cervical disc herniation
  • Cervical spondylolisthesis

You may not qualify if:

  • Infection
  • pregnancy
  • allergy to local anesthetic agents
  • previous cervical spine surgery

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Ji Hoon Park

Daegu, 42601, South Korea

RECRUITING

MeSH Terms

Conditions

Chronic Pain

Interventions

Anesthetics, Local

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

AnestheticsCentral Nervous System DepressantsPhysiological Effects of DrugsPharmacologic ActionsChemical Actions and UsesSensory System AgentsPeripheral Nervous System AgentsCentral Nervous System AgentsTherapeutic Uses

Central Study Contacts

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
CROSS SECTIONAL
Target Duration
1 Month
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

February 3, 2023

First Posted

February 10, 2023

Study Start

February 13, 2023

Primary Completion

November 30, 2023

Study Completion

November 30, 2023

Last Updated

February 15, 2023

Record last verified: 2023-02

Data Sharing

IPD Sharing
Will not share

Locations