Comparing the efficacy of preemptive analgesia and hematoma block with hematoma block alone in reduction of distal radius fracture

Phase 1

• Conditions: Preemptive analgesia in close reduction distal radius fracture; Preemptive analgesia, distal radius fracture

• Registration Number: TCTR202102040010
• Lead Sponsor: /A

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2021-02-04
• Study Completion: 2021-10-31
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Enrolling by invitation
• Sex: All
• Target Recruitment: 90

Inclusion Criteria

1. Distal radius fracture
2. Age > 18 yrsold

Exclusion Criteria

1.intraarticular distal radius fracture
2.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain score(VAS score) After reduction immediately,2,4,24 hr VAS score

Secondary Outcome Measures

Name	Time	Method
Pain score during reduction, analgesic consumption, complication, DASH score, side effect, Next day, 1wk DASH score