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erve block for surgery for mandible removal

Not Applicable
Completed
Conditions
Health Condition 1: null- Ca oral cavity ( buccal mucosa, lip, tongue) posted for mandibulectomyHealth Condition 2: C148- Malignant neoplasm of overlappingsites of lip, oral cavity and pharynxHealth Condition 3: C148- Malignant neoplasm of overlappingsites of lip, oral cavity and pharynx
Registration Number
CTRI/2017/09/009837
Lead Sponsor
Regional cancer centre
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
23
Inclusion Criteria

Adults posted for mandibulectomy

ASA PS 1&2

Who have given consent for the study

Exclusion Criteria

Refusal for consent, severe systemic illness, posted for arch mandibulectomy, coagulation abnormalities,, infection/ tutor at the site of block

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Consumption of opioids in the intraoperative periodTimepoint: During Tongue stitch , Dental extraction, condylotomy/osteotomy, Rise in Vitals more than 20% baseline value anytime during the procedure
Secondary Outcome Measures
NameTimeMethod
Hemodynamic stability in intraoperative periodTimepoint: Vital monitoring will be done every 5 minutes, during tongue stitch, dental extraction, condylotomy, osteotomy
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