Status:
WITHDRAWN
Superficial Cervical Plexus Block for Orthognathic Surgery
Lead Sponsor:
Medipol University
Conditions:
Maxillofacial Injuries
Maxillofacial Trauma
Eligibility:
All Genders
18-65 years
Phase:
NA
Brief Summary
US-guided superficial cervical plexus block (SCPB) may be used for several head and neck surgeries. Local anesthetic is injected under the sternocleidomastoid muscle for SCPB. It has lower complicatio...
Detailed Description
Postoperative pain management is very important in patients underwent orthognathic surgery. Effective pain control provides early mobilization, shorter hospital stay and it increases the satisfaction ...
Eligibility Criteria
Inclusion
- American Society of Anesthesiologists (ASA) classification I-II
- Scheduled for orthognathic surgery under general anesthesia
Exclusion
- history of bleeding diathesis,
- receiving anticoagulant treatment,
- known local anesthetics and opioid allergy,
- infection of the skin at the site of the needle puncture,
- pregnancy or lactation,
- patients who do not accept the procedure
Key Trial Info
Start Date :
June 22 2020
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
June 30 2022
Estimated Enrollment :
Patients enrolled
Trial Details
Trial ID
NCT04442009
Start Date
June 22 2020
End Date
June 30 2022
Last Update
May 4 2022
Active Locations (1)
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1
Istanbul Medipol University Hospital
Istanbul, Bagcilar, Turkey (Türkiye), 34070