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Trial registered on ANZCTR
Registration number
ACTRN12616000656437
Ethics application status
Approved
Date submitted
5/05/2016
Date registered
19/05/2016
Date last updated
26/11/2018
Date data sharing statement initially provided
26/11/2018
Type of registration
Prospectively registered
Titles & IDs
Public title
Distal skin temperature and tissue oxygen saturation for predicting ultrasound-guided lateral infraclavicular block success
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Scientific title
Evaluation of distal skin temperature and tissue oxygen saturation determined by near-infrared spectroscopy for predicting ultrasound-guided lateral infraclavicular block success
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Secondary ID [1]
289145
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Nil
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Forearm surgery
298658
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Condition category
Condition code
Anaesthesiology
298720
298720
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0
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Other anaesthesiology
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Intervention/exposure
Study type
Observational
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Patient registry
False
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
Forty patients between the ages of 18-65 yr, ASA physical status I and II, scheduled for acute or elective hand or forearm surgery under lateral infraclavicular block, will studied.Routine monitoring (consisting of a pulse oximeter, 3-lead ECG and a non-invasive blood pressure cuff ) will applied. In addition to this monitoring two near infrared spectroscopy sensors which will monitor tissue saturation (SomaSensors, Somanetics, Troy, MI) will be placed on each patient: One on the side of the peripheral nerve block and another at a similar site on the contralateral side.Each sensor will be placed on a different arm.The sensor will be placed on the the ventral aspect of the mid-forearm. The sensors will connected to a two channel monitor (Invos 5100B monitor, Somanetics), which automatically recorded digital data approximately every 7 s for a maximum of 30 min.Sensors record every 7 seconds for 30 minutes starting immediately prior to the administration of the block.
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Intervention code [1]
294750
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Early Detection / Screening
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Comparator / control treatment
Control group is the contralateral hand (the hand receiving no block).
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Control group
Active
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Outcomes
Primary outcome [1]
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Tissue oxygen saturation assesment by near-infrared spectroscopy
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Assessment method [1]
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Timepoint [1]
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A blind anesthesia nurse, recorded both sides tissue oxygen saturation values from the monitor at baseline, immediately after LIB and 1 min intervals for 30 min, starting immediately after performing LIB.
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Secondary outcome [1]
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Skin temperature assessment by skin temperature sensors.
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Assessment method [1]
323458
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Timepoint [1]
323458
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A blind anesthesia nurse, recorded both sides skin temperature at baseline, immediately after LIB and 1 min intervals for 30 min, starting immediately after performing LIB.
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Eligibility
Key inclusion criteria
18-65 yr, ASA physical status I and II, scheduled for acute or elective hand or forearm surgery under lateral infraclavicular block
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Minimum age
18
Years
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Maximum age
65
Years
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Age less than 18 years, morbid obesity defined as body mass index (BMI) greater than 40, international normalised ratio more than 1.4, platelet count less than 80000 ,coagulopathy, medication with vitamin K antagonists, high-dose or fractionated heparin treatment, allergy to local anaesthetics, infection at the site of needle insertion, peripheral neurological disease, Raynaud’s phenomenon and patient refusal.
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Study design
Purpose
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Duration
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Selection
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Timing
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
15/06/2016
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Actual
15/06/2016
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Date of last participant enrolment
Anticipated
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Actual
1/09/2018
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Date of last data collection
Anticipated
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Actual
1/09/2018
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Sample size
Target
40
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Accrual to date
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Final
40
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Recruitment outside Australia
Country [1]
7859
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Turkey
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State/province [1]
7859
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Konya
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Funding & Sponsors
Funding source category [1]
293521
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Hospital
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Name [1]
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Konya Training and Research Hospital
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Address [1]
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Konya Training and Research Hospital, Haci Saban Mah. Meram Yeniyol Caddesi No:97 Meram KONYA, Postcode:42090
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Country [1]
293521
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Turkey
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Primary sponsor type
Hospital
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Name
Konya Training and Research Hospital
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Address
Konya Training and Research Hospital, Haci Saban Mah. Meram Yeniyol Caddesi No:97 Meram KONYA, Postcode:42090
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Country
Turkey
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Secondary sponsor category [1]
292343
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None
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Name [1]
292343
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Address [1]
292343
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Country [1]
292343
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
294962
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Necmettin Erbakan University Meram School of Medicine
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Ethics committee address [1]
294962
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Necmettin Erbakan University Meram School of Medicine, Akyokus, Meram-Konya 42080
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Ethics committee country [1]
294962
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Turkey
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Date submitted for ethics approval [1]
294962
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14/02/2016
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Approval date [1]
294962
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19/02/2016
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Ethics approval number [1]
294962
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2016/464
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Summary
Brief summary
Forty patients will be studied for this study. Routine monitoring (consisting of a pulse oximeter, 3-lead ECG and a non-invasive blood pressure cuff ) will applied. In addition to this monitoring two sensors (SomaSensors, Somanetics, Troy, MI) will be placed on each patient: One on the side of the peripheral nerve block and another at a similar site on the contralateral side. The sensor will be placed on the the ventral aspect of the mid-forearm. The sensors will connected to a two channel monitor (Invos 5100B monitor, Somanetics), which automatically recorded digital data approximately every 7 s for a maximum of 30 min. A blind anesthesia nurse, will record both sides skin temperature at baseline, immediately after LIB and 1 min intervals for 30 min, starting immediately after performing LIB.A blind anesthesia nurse, will record both sides tissue oxygen saturation values from the monitor at baseline, immediately after LIB and 1 min intervals for 30 min, starting immediately after performing LIB.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Dr Mehmet SARGIN
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Address
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Konya Training and Research Hospital, Anesthesiology and Reanimation Department, Haci Saban Mah. Meram Yeniyol Caddesi No:97 Post code: 42090 Meram KONYA
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Country
65638
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Turkey
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Phone
65638
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+905322662766
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Fax
65638
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Email
65638
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[email protected]
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Contact person for public queries
Name
65639
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Mehmet SARGIN
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Address
65639
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Konya Training and Research Hospital, Anesthesiology and Reanimation Department, Haci Saban Mah. Meram Yeniyol Caddesi No:97 Post code: 42090 Meram KONYA
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Country
65639
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Turkey
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Phone
65639
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+905322662766
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Fax
65639
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Email
65639
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[email protected]
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Contact person for scientific queries
Name
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Mehmet SARGIN
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Address
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Konya Training and Research Hospital, Anesthesiology and Reanimation Department, Haci Saban Mah. Meram Yeniyol Caddesi No:97 Post code: 42090 Meram KONYA
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Country
65640
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Turkey
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Phone
65640
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+905322662766
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Fax
65640
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Email
65640
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[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
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No/undecided IPD sharing reason/comment
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What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
Source
Title
Year of Publication
DOI
Dimensions AI
Evaluation of distal skin temperature and tissue oxygen saturation determined by near-infrared spectroscopy for predicting ultrasound-guided lateral infraclavicular block success
2022
https://doi.org/10.17085/apm.22181
N.B. These documents automatically identified may not have been verified by the study sponsor.
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