WithdrawnNot Applicable

Superficial Cervical Plexus Block for Orthognathic Surgery

Stopped: No participants

Turkey (Türkiye)0Started 2020-06-22

Plain-language 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 complication rate compared to the deep cervical plexus block. Postoperative pain management is important in patients underwent orthognathic surgery. Effective pain treatment provides early mobilization, and shorter hospital stay.

Who can participate

Age range18 Years – 65 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * American Society of Anesthesiologists (ASA) classification I-II * Scheduled for orthognathic surgery under general anesthesia Exclusion Criteria: * 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

What they're measuring

Opioid consumption

Timeframe: Change from baseline opioid consumption at postoperative 1, 2, 4, 8, 16, and 24 hours

Trial details

NCT IDNCT04442009

SponsorMedipol University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2022-05-30

View on ClinicalTrials.gov More Maxillofacial Injuries trials