Thoracic Combined Spinal Epidural Anesthesia for Breast Surgery
NCT ID: NCT04706247
Last Updated: 2021-05-18
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
26 participants
OBSERVATIONAL
2021-01-04
2021-05-17
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Interventions
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thoracic combined spinal epidural anesthesia
A combined spinal-epidural anesthesia set will be used for the block. Using the loss of resistance to saline technique, an 18 G Tuohy needle will be advanced to the T2-3 vertebral interspace with the mid-line approach. After confirming the epidural space, a 26 G pencil point spinal needle will be inserted slowly through the Tuohy needle to puncture the dura. After free flow of cerebrospinal fluid will be observed, local anesthetic wil be injected into the subarachnoid space over 15 secs. Then, an epidural catheter will be inserted into the epidural space.
Eligibility Criteria
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Inclusion Criteria
* American Society of Anesthesiologists (ASA) physical status classification groups I or II
Exclusion Criteria
* presence of any condition complicating and contraindicating spinal epidural anesthesia.
18 Months
70 Months
FEMALE
No
Sponsors
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Antalya Training and Research Hospital
OTHER_GOV
Responsible Party
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Principal Investigators
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Lutfi Ozyurek, M.D.
Role: STUDY_DIRECTOR
Antalya Training and Research Hospital
Locations
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Antalya Training and Research Hospital
Antalya, , Turkey (Türkiye)
Countries
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Other Identifiers
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lutfi1
Identifier Type: -
Identifier Source: org_study_id
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