Study of the effect of steroid addition of nerve block in hip fracture surgery

Not Applicable

• Conditions: Proximal femoral fracture

• Registration Number: JPRN-UMIN000050714
• Lead Sponsor: Shimura Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2023-04-10
• Study Completion: 2024-01-31
• Last Update Posted: 2 September 2024

Recruitment & Eligibility

• Status: Complete: follow-up continuing
• Sex: All
• Target Recruitment: 120

Inclusion Criteria

Not provided

Exclusion Criteria

1.Patients who cannot complain of pain or patients who cannot administer NSAIDs or acetaminophen 2.Patients who received NSAIDs or acetaminophen within 3 hours before entering the operating room to immediately after surgery 3.Subjects who have diabetes or prone to infections 4.Others who have been determined ineligible by principal investigator or sub-investigator

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Duration from FICB administration to first as-needed analgesic administration

Secondary Outcome Measures

Name	Time	Method
umber of doses of as-needed analgesics (within 48 hours from FICB) Safety evaluation items: Vital sign changes such as postoperative hypotension (within 48 hours from FICB) Prolongation of motor block of the affected limb (within 48 hours from FICB) Local infection (within 1 week after surgery)