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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04222192
Other study ID # 2011-KAEK-25 2019/12-09
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 15, 2020
Est. completion date January 30, 2021

Study information

Verified date December 2022
Source Bursa Yüksek Ihtisas Education and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The nerve blocks applied with ultrasonography are used for pain and operation after many operations today. Applications with ultrasonography shorten the processing time, reduce the amount of local anesthetic used and lead to fewer complications. However, the use of ultrasonography is not so common in neuraxial regional anesthesia applications. In the literature, epidural applications accompanied by ultrasonography were applied with different approaches.


Description:

In this study the investigators will used the two different ultrasound -guided epidural block approach . Paramedian sagittal oblique and Transverse interlaminar. The investigators will used this two technique in epidural catheter placement using the real-time ultrasound.


Recruitment information / eligibility

Status Completed
Enrollment 90
Est. completion date January 30, 2021
Est. primary completion date January 15, 2021
Accepts healthy volunteers No
Gender All
Age group 25 Years to 85 Years
Eligibility Inclusion Criteria: - Patients who were in the American Society of Anesthesiologists (ASA) I-III class - Patients whom need medical epidural anesthesia - Patients with consent to participate in the study Exclusion Criteria: - Patients with a known history of back surgery - Bleeding diathesis disorder - Allergy to local anesthetics - Patient refusal

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Epidural block
Epidural catheter insertions

Locations

Country Name City State
Turkey Bursa Yuksek Ihtisas Training and Research Hospital Bursa

Sponsors (1)

Lead Sponsor Collaborator
Bursa Yüksek Ihtisas Education and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of needle routing number of needle redirects forming successful block 20 minutes
Primary Epidural catheter placement time time (minutes) until the epidural catheter is inserted 20 minutes
Secondary Epidural igne visibility degree 4 = Excellent visibility, 3 = Medium visibility, 2 = Weak visibility 1 = No visibility using a 4-point Likert scale by the practitioner 20 minutes
Secondary Difficulty of catheter placement Assessed by the Practitioner using a 10-point scale, 0: easiest, 10: hardest) 30 minutes
Secondary distance measurement of neuraxial structures Anterior and posterior complex distance measured during epidural administration.
Distance from skin to anterior aspect of ligament flavum (cm)
Distance from skin to posterior dura (cm)
30 minutes
Secondary Patient position Patient position during epidural placement Sitting Lateral 20 minutes
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