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effect of posterior tibial nerve block on hallux valgus surgery

Evaluation of the effect of tibialis posterior nerve block on postoperative pain and functional outcomes of patients undergoing hallux valgus surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200525047569N1
Enrollment
60
Registered
2021-09-23
Start date
2021-08-23
Completion date
Unknown
Last updated
2021-11-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ptients with hallus valgus deformity. Hallux valgus (acquired), unspecified foot

Interventions

Intervention 1: Intervention group: peripheral nerve blockage of posterior tibial concurrent with spinal block of hallux valgus surgery.5 ml bupivacaine 0.5% will be administered to posterior tibial n

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 65 Years

Inclusion criteria

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

Exclusion criteria: peripheral neuropathy ankle joint degenerative changes ankle joint muscle weekness

Design outcomes

Primary

MeasureTime frame
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

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

Countries

Iran (Islamic Republic of)

Contacts

Public Contact?Amir Sabaghzadeh

Shahid Beheshti University of Medical Sciences

dramirsabbaghzadeh@gmail.com+98 21 25719

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026