effect of posterior tibial nerve block on hallux valgus surgery

Not Applicable

Recruiting

• Conditions: Ptients with hallus valgus deformity.; Hallux valgus (acquired), unspecified foot; M20.10

• Registration Number: IRCT20200525047569N1
• Lead Sponsor: Shahid Beheshti University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 1 November 2021

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

age between 20-65
no other previous surgery of foot
no rheumatologic disease
Lack of sensitivity to anesthetic drugs
hallux valgus deformity moderate to severe

Exclusion Criteria

peripheral neuropathy
ankle joint degenerative changes
ankle joint muscle weekness

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
VAS ( visual analog score ). Timepoint: 6,12,24 hours after hallux valgus deformity surgery. Method of measurement: VAS ( visual analogue score ).;Fentanyl intake every 6 hours after hallux valgus surgery. Timepoint: 6,12,24 hours after hallux valgus deformity surgery. Method of measurement: Based on patient addmission profile in orthopedic ward.;?AOFAS ( American orthopedic association foot and ankle surgery) score. Timepoint: 6,12,24 hours after hallux valgus deformity surgery. Method of measurement: The American Orthopedic Foot and Ankle Score (AOFAS) questionnaire.

Secondary Outcome Measures

Name	Time	Method
Sleep hours during 24 hours after hallux valgus deformity surgery. Timepoint: During 24 hours after surgery. Method of measurement: Patients record in orthopedic ward.