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Effect of Infraclavicular and Interscalen Block on Oxygenitaon of the Forearm

Effect of Infraclavicular and Interscalen Block on Oxygenitaon of the Forearm : Randomized Controlled Study.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04748211
Enrollment
104
Registered
2021-02-10
Start date
2018-06-15
Completion date
2019-06-15
Last updated
2021-02-12

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

Conditions

Upper Extremity Fracture

Brief summary

to research the oxygenitaon effects of infraclavicular and interscalene blocks on the forearm.

Detailed description

To research the oxygenation effects of infraclavicular and interscalen blocks on the forearm by comparing the blood flow (BF) values using the USG, Perfusion index (PI) and Near infrared spectroscopy (NIRS) values using the massimo device.

Interventions

USI and neurostimulator guided infraclavicular block, 10 ml 2% lidocain and 10 ml 0.05% marcaine was administered for local anetshesia. After the block was administered MAP, HR, TAV, BAD, BAA, BF, PI and rSO 2 values were measured and recorded at the 10th, 20th, and 30th minutes.

PROCEDUREInterscalen Block

USI and neurostimulator guided interscalen block, 10 ml 2% lidocain and 10 ml 0.05% marcaine was administered for local anetshesia. After the block was administered MAP, HR, TAV, BAD, BAA, BF, PI and rSO 2 values were measured and recorded at the 10th, 20th, and 30th minutes.

Sponsors

Bulent Ecevit University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Intervention model description

The study will be a two-arm parallel assignment. One group will receive infraclavicular block and the other will receive interscalen block

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* aged between 18-65 * ASA Score I-III * undergoing elective or emergency arm, elbow and forearm surgery

Exclusion criteria

* Patient's refusal for Brachial Plexus Blockage * Patients who had any neurological disorders preventing the evaluation of the sensory block in the upper extremity, * Infection in the area to be blocked with ICB or ISB, * Non-cooperated patients * Patients with coagulopathy, * Morbidly obese patients * Patients with diabetes mellitus * Patients with hypertension * Patients with peripheral artery disease * Patients with allergy to the drugsto be used * Patients who had trauma in the area scheduled for the block * Paitens who had deterioration of anatomical integrity because of previous surgery * Pregnant women * Patients whose block failed

Design outcomes

Primary

MeasureTime frameDescription
oxygenation of the forearmduring the procedure three timesto compare the oxygenation of the forearm by measuring perfusion index device

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026