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Clinical Trials/JPRN-UMIN000002005
JPRN-UMIN000002005
Completed
Phase 3

Effects of low-intensity pulsed ultrasound (LIPUS) treatment in post-operative scaphoid delayed unions or nonunions: multi-institutional prospective randomized controlled trial - Effects of low-intensity pulsed ultrasound (LIPUS) treatment in post-operative scaphoid delayed unions or nonunions

Japanese Society for Surgery of the Hand, Tsukuba Critical Path Research and Education Integrated Leading Center (CREIL)0 sites86 target enrollmentJune 1, 2009

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
scaphoid delayed unions and nonunions
Sponsor
Japanese Society for Surgery of the Hand, Tsukuba Critical Path Research and Education Integrated Leading Center (CREIL)
Enrollment
86
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
June 1, 2009
End Date
April 30, 2013
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Japanese Society for Surgery of the Hand, Tsukuba Critical Path Research and Education Integrated Leading Center (CREIL)

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1\) Scaphoid partially united fractures 2\) The scaphoid delayed unions or nonunions treating with vascularized bone grafting 3\) The patient presented arthritis of the wrist 4\) The proximal pole nonunions with avascular necrosis, which was proved with MRI 5\) The patient receiving LIPUS treatment before 6\) The patient receiving electrical stimulation 7\) The patient who is unable to apply LIPUS treatment 8\) The patient had recent severe systemic past history such as heart, liver or kidney disease 9\) The patient had treated cancer therapy within recent five years 10\) The patient is pregnant or possible pregnant 11\) The patient entering for other medical trials 12\) The patient who is unable to comply with this study protocol 13\) The patient who is unable to comply with the consent form of this study 14\) The patient who was recognized unsuitable for this study by primary physician

Outcomes

Primary Outcomes

Not specified

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