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Comparison of postoperative dysphagia between local 80 vs 40 mg methyprednisolone application following multilevel anterior cervical discectomy and fusion : a double-blinded, prospective, randomized controlled trial

Phase 4
Conditions
CSMCSRpostoperative dysphagia
CSR
CSM
postoperative dysphagia
Registration Number
TCTR20240627005
Lead Sponsor
maharat nakhon ratchasima hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Enrolling by invitation
Sex
All
Target Recruitment
60
Inclusion Criteria

CSM CSR PATIENT WHO UNDERGO >= 2 LEVEL OF ACDF WITH PLATING OPERATION
AGE MORE THAN 20 YEARS OLD

Exclusion Criteria

INFLAMMATORY DISEASE EX. RA, AS ANY OPERATION FOR TRAUMA
ANY INFECTION
PRIOR STEROID USED
EAT-10 SCORE >= 3 PREOP
DENIED TO ENROLLED THIS STUDY

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Dysphagia rate Postoperative day 3 , follow up 2 weeks and 6 weeks Eating Assessment tool(EAT-10) score
Secondary Outcome Measures
NameTimeMethod
disability point in patients with neck pain Postoperative day 3 , follow up 2 weeks and 6 weeks Neck disability Index
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