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Tightrope or Screw Fixation of Acute Tibiofibular Syndesmotic Injury (TIGHTROPE-SS)

Primary Purpose

Syndesmotic Injury of the Ankle

Status
Completed
Phase
Not Applicable
Locations
Norway
Study Type
Interventional
Intervention
Tightrope Syndesmosis Repair Kit
Syndesmotic screw
Sponsored by
Sykehuset Asker og Baerum
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Syndesmotic Injury of the Ankle focused on measuring Syndesmosis, Injury, Ankle, Fracture

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 18 to 70 years
  • Acute syndesmotic injury with or without Weber type C fracture

Exclusion Criteria:

  • Prior injury of the same ankle
  • Severe injury of same leg affecting rehabilitation
  • Symptomatic osteoarthritis of same ankle
  • Open injury
  • Decubital injury affecting surgical site
  • Dementia or unable to sign informed consent
  • Neuropathic conditions affecting same leg

Sites / Locations

  • Oslo University Hospital
  • Baerum Hospital, Vestre Viken

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Tightrope

Syndesmotic screw

Arm Description

Treatment with Tightrope Syndesmosis Repair Kit

Treatment with a quadricortical syndesmotic screw

Outcomes

Primary Outcome Measures

OTA Score (Modified American Orthopaedic Foot and Ankle Society ankle hind foot score)
Modified American Orthopaedic Foot and Ankle Society ankle hind foot score (0-100)

Secondary Outcome Measures

Olerud-Molander Ankle (OMA) Score
Dorsiflexion angle
According to Lindsjø
Health-related quality of life (EQ-5D)
CT measurements of syndesmotic distance

Full Information

First Posted
January 11, 2011
Last Updated
April 17, 2018
Sponsor
Sykehuset Asker og Baerum
Collaborators
Oslo University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT01275924
Brief Title
Tightrope or Screw Fixation of Acute Tibiofibular Syndesmotic Injury
Acronym
TIGHTROPE-SS
Official Title
Tightrope or Screw Fixation of Acute Tibiofibular Syndesmotic Injury. Randomised Controlled Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
April 2018
Overall Recruitment Status
Completed
Study Start Date
January 2011 (undefined)
Primary Completion Date
March 2015 (Actual)
Study Completion Date
April 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Sykehuset Asker og Baerum
Collaborators
Oslo University Hospital

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Syndesmotic injuries are common and often associated with unstable ankle fractures. The most common treatment is with a syndesmotic screw through the fibula and tibia which is later removed, usually after 10-12 weeks. The Tightrope Syndesmosis Repair Kit (Arthrex; Naples, Florida). is used for the same indication, it consists of a heavy suture placed across the syndesmosis which has been looped and tightened through cortical button anchors on either side of the ankle. It does not need removal and thus avoids subsequent surgery. This trial compares these two treatment methods for syndesmotic injuries of the ankle.
Detailed Description
Patients 18-70 years presenting to one of the two hospitals with an acute syndesmotic injury are eligible for inclusion. 50 patients are randomised to two treatment groups: One group receives a Tightrope (R) fixation and the other receives a quadricortical screw fixation which is removed after 12 weeks. Follow-up intervals are at 6 weeks, 6, 12 and 24 months with standardised CT scans postoperatively and at 12, 24 months and 5 years clinical end-ponts/scores.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Syndesmotic Injury of the Ankle
Keywords
Syndesmosis, Injury, Ankle, Fracture

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
97 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Tightrope
Arm Type
Active Comparator
Arm Description
Treatment with Tightrope Syndesmosis Repair Kit
Arm Title
Syndesmotic screw
Arm Type
Active Comparator
Arm Description
Treatment with a quadricortical syndesmotic screw
Intervention Type
Device
Intervention Name(s)
Tightrope Syndesmosis Repair Kit
Other Intervention Name(s)
Tightrope Syndesmosis Repair Kit, Arthrex; Naples, Florida
Intervention Description
Tightrope Syndesmosis Repair Kit
Intervention Type
Device
Intervention Name(s)
Syndesmotic screw
Other Intervention Name(s)
Cortical screw; Synthes GmbH, Switzerland
Intervention Description
Quadricortical syndesmotic screw
Primary Outcome Measure Information:
Title
OTA Score (Modified American Orthopaedic Foot and Ankle Society ankle hind foot score)
Description
Modified American Orthopaedic Foot and Ankle Society ankle hind foot score (0-100)
Time Frame
5 years
Secondary Outcome Measure Information:
Title
Olerud-Molander Ankle (OMA) Score
Time Frame
5 years
Title
Dorsiflexion angle
Description
According to Lindsjø
Time Frame
5 years
Title
Health-related quality of life (EQ-5D)
Time Frame
5 years
Title
CT measurements of syndesmotic distance
Time Frame
5 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 18 to 70 years Acute syndesmotic injury with or without Weber type C fracture Exclusion Criteria: Prior injury of the same ankle Severe injury of same leg affecting rehabilitation Symptomatic osteoarthritis of same ankle Open injury Decubital injury affecting surgical site Dementia or unable to sign informed consent Neuropathic conditions affecting same leg
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wender Figved, MD, PhD
Organizational Affiliation
Baerum Hospital, Vestre Viken, Norway
Official's Role
Study Director
Facility Information:
Facility Name
Oslo University Hospital
City
Oslo
ZIP/Postal Code
0407
Country
Norway
Facility Name
Baerum Hospital, Vestre Viken
City
Rud
ZIP/Postal Code
1351
Country
Norway

12. IPD Sharing Statement

Learn more about this trial

Tightrope or Screw Fixation of Acute Tibiofibular Syndesmotic Injury

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