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Bone Tunnel Widening Following ACL Reconstruction

This study has been completed.
Sponsor:
Collaborator:
Inion Oy
Information provided by (Responsible Party):
Hospital for Special Surgery, New York
ClinicalTrials.gov Identifier:
NCT00198042
First received: September 13, 2005
Last updated: May 16, 2017
Last verified: May 2017
  Purpose

Hypothesis 1: There is less tunnel-widening with bone-patella tendon-bone graft compared with the hamstring graft when the same fixation method is used. Tunnel widening is greater with achilles tendon allografts versus autograft bone-patella tendon-bone and hamstring autografts.

Hypothesis 2: Tunnel widening occurs in the early post-operative period (< 8 weeks) when the tendon remodels within the bone tunnels.

Hypothesis 3: Low pre-operative bone mineral density is associated with tunnel widening.


Condition Intervention
Anterior Cruciate Ligament Injury Knee Injuries Procedure: Surgical reconstruction of the ACL

Study Type: Interventional
Study Design: Intervention Model: Single Group Assignment
Masking: No masking
Primary Purpose: Treatment
Official Title: Bone Tunnel Widening Following ACL Reconstruction

Resource links provided by NLM:


Further study details as provided by Hospital for Special Surgery, New York:

Primary Outcome Measures:
  • Bone Tunnel Diameter [ Time Frame: 2 years ]
    Bone tunnel diameter measured on MRI


Other Outcome Measures:
  • Bone Tunnel Cross Sectional Area [ Time Frame: 2 years ]

Enrollment: 18
Study Start Date: June 2004
Study Completion Date: December 31, 2015
Primary Completion Date: December 31, 2015 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Surgical Reconstruction of the ACL Procedure: Surgical reconstruction of the ACL
Surgical reconstruction of the ACL

  Show Detailed Description

  Eligibility

Ages Eligible for Study:   18 Years to 55 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Individuals within the age range of 18 to 55 years who are diagnosed with anterior cruciate insufficiency and have decided to undergo ACL reconstruction using autogenous graft will be included in the study.

Exclusion Criteria:

  • Individuals that have previous knee surgeries, multi-ligament injuries, systemic ligament disorders such as Ehlers Danlos syndrome or connective tissue disorders will be excluded from the study.
  • Individuals who are pregnant or expect to be pregnant during the course of the study or who are especially concerned with X-ray exposure should also be excluded.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00198042

Locations
United States, New York
Hospital for Special Surgery
New York, New York, United States, 10021
Sponsors and Collaborators
Hospital for Special Surgery, New York
Inion Oy
Investigators
Principal Investigator: Scott Rodeo, MD Hospital for Special Surgery, New York
  More Information

Responsible Party: Hospital for Special Surgery, New York
ClinicalTrials.gov Identifier: NCT00198042     History of Changes
Other Study ID Numbers: 22129
Study First Received: September 13, 2005
Results First Received: March 20, 2017
Last Updated: May 16, 2017

Keywords provided by Hospital for Special Surgery, New York:
ACL
Tunnel
Widening

Additional relevant MeSH terms:
Wounds and Injuries
Knee Injuries
Leg Injuries

ClinicalTrials.gov processed this record on June 22, 2017