Segment Transport Versus Acute Shortening In The Treatment of Tibial Pseudarthroses With Bone Loss

• Sponsor: Bezmialem Vakif University (Other)
• Overall Status: Completed
• CT.gov ID: NCT01246934
• Collaborator: (none)
• Enrollment: 22
• Location: 1
• Arm: 1
• Duration (Months): 4
• Patients Per Site Per Month: 5.4

Study Details

Study Description

Brief Summary

In this study the investigators are presenting the advantages as well as the disadvantages of ACUTE SHORTENING AND RELENGTHENINIG VS SEGMENT TRANSPORT methods.

Condition or Disease	Intervention/Treatment	Phase
TIBIA PSEUDOARTHROSES	Other: ASR METHOD	N/A

Study Design

• Study Type: Interventional
• Actual Enrollment: 22 participants
• Allocation: Non-Randomized
• Intervention Model: Parallel Assignment
• Masking: Single (Investigator)
• Primary Purpose: Treatment
• Study Start Date: Oct 1, 2009
• Actual Primary Completion Date: Dec 1, 2009
• Actual Study Completion Date: Feb 1, 2010

Arms and Interventions

Arm	Intervention/Treatment
No Intervention: COMPLICATION	Other: ASR METHOD

Outcome Measures

Primary Outcome Measures

1. TREATMENT PERIOD AND COMPLICATION RATE []

Eligibility Criteria

Criteria

• Ages Eligible for Study: 13 Years to 50 Years
• Sexes Eligible for Study: All

Inclusion Criteria:TIBIA PSEUDOARTHROSES -

Exclusion Criteria:BONE LOSS GREATER THAN 10 CM

-

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Cengiz Sen	Istanbul		Turkey	34290

Sponsors and Collaborators

• Bezmialem Vakif University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• ClinicalTrials.gov Identifier: NCT01246934
• Other Study ID Numbers: BVUORT001
• First Posted: Nov 24, 2010
• Last Update Posted: Nov 24, 2010
• Last Verified: Nov 1, 2010

• Additional relevant MeSH terms: Pseudarthrosis

Study Results

No Results Posted as of Nov 24, 2010