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Post Operative Ankle Splint Study - Prospective Multi Center Randomized Controlled Trial (PASS)

Primary Purpose

Ankle Fractures, Splints

Status
Completed
Phase
Not Applicable
Locations
Kuwait
Study Type
Interventional
Intervention
Splinting (plaster of paris)
Sponsored by
Kuwait Institute for Medical Specialization
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Ankle Fractures

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • A.O 44 ankle fractures requiring surgical fixation (uni or bimalleolar with /without syndesmotic injury)

Exclusion Criteria:

  • pathological fracture
  • poly trauma pilon fractures open fractures other associated fractures in same extremity peripheral neuropathy

Sites / Locations

  • Mubarak Al kabeer hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

No Intervention

Arm Label

post operative Ankle fractures with splint

post operative Ankle fractures without splint

Arm Description

All patient who meet the inclusion criteria of having ankle fracture that rigidly fixed and randomized to receive splint post operative

All patient who meet the inclusion criteria of having ankle fracture that rigidly fixed and randomized to receive NO splint post operative

Outcomes

Primary Outcome Measures

Assessing the change in the level of pain between the splint and no-splint groups
Visual analogue scale (0;lowest pain, 10;highest pain)
Assessing the change in ankle swelling from 2 weeks postop to 1 year postop in the splint and no-splint groups
Measuring tape to assess supramalleolar, mid-foot, and mid-calf circumference

Secondary Outcome Measures

Change in the functional scoring system used below
The American Orthopaedic Foot and Ankle Society (AOFAS) Ankle-Hindfoot Score
Number of participants with; infection, nonunion, deep-vein thrombosis, stiffness, equinus
Rate of infection, nonunion, deep-vein thrombosis, stiffness, equinus

Full Information

First Posted
March 6, 2021
Last Updated
March 7, 2023
Sponsor
Kuwait Institute for Medical Specialization
Collaborators
Kuwait University
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1. Study Identification

Unique Protocol Identification Number
NCT04796168
Brief Title
Post Operative Ankle Splint Study - Prospective Multi Center Randomized Controlled Trial
Acronym
PASS
Official Title
Post Operative Ankle Splint Study - Prospective Multi Center Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Completed
Study Start Date
February 1, 2021 (Actual)
Primary Completion Date
March 1, 2023 (Actual)
Study Completion Date
March 1, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Kuwait Institute for Medical Specialization
Collaborators
Kuwait University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Background: Ankle fractures are some of the most common orthopedic presentations, however, controversy in their management and their post-operative rehabilitation protocols exist. Most displaced ankle fractures treated with anatomical reduction and stable internal fixation to allow early range of motion by allowing rigid fixation and restoration of ankle joint congruence. Post-operative rehabilitation protocols varies between surgeons and institutions with the majority emphasising early rehabilitation protocols. The use of a splint. The rational for splinting ankle fractures after rigid fixation is to decrease pain level, rest the soft tissues and prevent equinus deformity. Up to date there is no scientific research to question the benefit of routine use of splints after rigid fixation of ankle fractures. Methods: A prospective multi-centre randomised control trial. Approximately fifty patients will be enrolled from 3 hospitals (Adan, Mubarak and Farwaniya hospital) over a 1 year period. The studied sample will be randomised into 2 groups using computerised randomisation software: splint group and no-splint group. The patients will be examined at set intervals for pain, swelling, deep-vein thrombosis and a set of scoring tools. The tools include: visual analogue score (VAS) for pain, Short Form Health Survey (SF-36), American Orthopaedic Foot and Ankle Society (AOFAS) Ankle-Hindfoot score, physical and radiological assessment at 2 weeks, 3 months, 6 months and 1 year intervals. Statistical Package for the Social Sciences program (SPSS) will be used for statistical analysis Results/outcomes: Functional scores, symptoms and signs, complications, radio-graphic and clinical follow up will be recorded.
Detailed Description
Overview The mainstay of unstable ankle fractures is surgical in nature, however controversy and an unclear consensus exists regarding post-operative rehabilitation; is a splint necessary or not? Splinting the ankle post-op is traditionally used to reduce pain and limit motion. However, the evidence is unclear and benefits are not well established. Further, splinting the ankle in the traditional back-slab is accompanied by complications including; pressure sores, skin irritation and deep-vein thrombosis. There is incomplete evidence supporting early commencement of weight-bearing and the use of a detachable type of immobilization to allow exercise during the immobilization period after surgical fixation(1). It is also noteworthy that its believed that because of the potential increased risk of adverse events, the patient's compliance with the use of a removable type of immobilisation to enable controlled exercise is essential(1). To date there is lacking scientific research to question the benefit of routine use of splints after rigid fixation of ankle fractures. There is little evidence that any specific rehabilitation program improves clinical outcome (2). One study found that active ankle movements in combination with weight bearing facilitate and improve the rehabilitation following operation for an ankle fracture [3]. A systematic review of 38 controlled trials related to the rehabilitation of ankle fractures found that early ambulation post-op may improve ankle range of motion, yet with limited quality evidence [3, 6]. . Early performance of ankle exercises following surgical fixation improved ankle function and mobility, while decreasing pain, but was associated with higher rates of adverse events (e.g. surgical wound complications), although most problems were minor(3). Use of a removable immobilization device was necessary for this approach. It could be plausible that determent and harm to the patient is being done in the form of dermatological adverse effects of splints if there is in fact no benefit to their use. There is a clear need to define whether or not a splint is needed for the sake of patient safety and comfort postoperatively. Research Question/Hypothesis What are the benefits and risks of splinting ankle fractures post-op. The investigators believe that there is no considerable benefit to splinting ankle fractures after fixation, in fact, splinting may even result in stiffness, cast-associated complications and reduced patient satisfaction. Objectives and aims Overall Objective To critically assess the benefits of splints after rigid fixation of ankle fractures. Specific Aims 1- To assess the level of pain between the splint and no-splint groups. 2- To compare the range of motion between the splint and no-splint groups. Secondary objectives To assess patient satisfaction between the splint and no-splint groups. To assess other complications and radiological finding differences between the splint and no-splint groups. To check the difference in time-to-union between the splint and no-splint groups. BACKGROUND AND SIGNIFICANCE Ankle fractures Over five million ankle injuries occur each year in the United States alone, and the incidence of these fractures is approximately 187 fractures per 100,000 people each year (4). This figure has been increasing, most probably because of the exponential growth of the population and the growing amount of people practising sports(4). Cigarette smoking and a high body mass index have been associated with ankle fractures(5, 6). Ankle fractures can be categorised into stable and unstable fractures. Isolated malleolar fractures are usually stable if they are not displaced but, care should be taken with fractures of the medial malleolus. Disturbance of nearby structures often occurs in association with these fractures, and they sometimes appear to be isolated injuries at first. Bimalleolar Fractures, which is fracture of both the lateral and medial malleoli, are generally unstable. Trimalleolar fractures are unstable and typically occur with injuries of greater force. These are bimalleolar fractures with a fracture of the posterior malleolus. Fracture stability determines treatment. Emergent conditions, such as an open fracture or neurovascular impairment, necessitate surgical consultation and treatment. Fracture dislocations must be reduced to avoid serious complications, such as avascular necrosis. After emergency situations are excluded, the fracture should be evaluated more closely, with focus on any malalignment or instability, to determine proper management. Standard treatment for stable ankle is Immobilization in a cast (CI) for approximately six weeks but, new evidence is growing and supporting that shorter periods of casting allows a similar level of healing with less risk of complications. A randomized trial of 247 adults with stable fractures of the lateral malleolus, 3 week long immobilization in a short-leg walking cast or rigid ankle orthosis reduced the short-term loss of ankle mobility and the risk for deep vein thrombosis as compared with care, without compromising fracture healing(4). Confirmation of these results is needed, but 3 weeks of immobilization may be a reasonable approach in healthy adults with uncomplicated fractures. Unstable ankle fractures are treated surgically. Research design and methods Overview The PASS Trial is going to be a 1-2 year long randomised control trial where a qualified team of doctors will administer a questionnaire, take clinical examination results, and assign patients to treatment groups of splint and non-splint post-surgical repair. Range of motion will be evaluated with a Goniometer and information will be gathered in a standardized manner. Patients aged 18-65 taken from Adan, Mubarak, and Farwaniya hospitals will be consented and randomly assigned to a treatment group after which they will be followed periodically at their designated follow up appointments, which are at 2 weeks, 3 months, 6 months and 1 year. Patients will be collected over the duration of 2 years until a quota of 50-75 participants is achieved. Only isolated A.O 44 ankle fractures requiring surgical fixation will be included in the study. Pathological fractures, polytrauma patients and open fractures will be excluded. Strengths and weaknesses of the study Study Design This study is a double blinded Randomized Control Trial to eliminate as much bias as possible. All Principle investigators who measured the results are near equal in terms of experience and education. Methods of gathering and collecting data as well as tools to do so were standardized. Our study will utilize multivariate regression models and intention to treat analysis. The study covers the major trauma centres in Kuwait providing adequate representation of the population. Recall bias is minimized due to close proximity of questioning and the event. Potential Limitations Patient compliance to treatment arms is the main potential issue of our study. The extent of non-compliance was measured through questionnaire. There is a lack of literature on this subject, which results in deficient comparison with other populations around the globe and in the region. Public health significance On the Individual Level The Patients as individuals will feel liberated as they may no longer consider themselves disabled and diseased while they are not wearing a split providing physiological relief. This benefit could even translate to earlier return to work and benefit society. Individuals will no longer be inconvenienced by being required to wear a splint. On The Global Level It is in the interest of public health care systems to conduct this trial because there is a possibility that the costs of splints provide by the hospitals will be cut and put to better use. Such a trial could impact public health policy because it can provide good evidence to change the current standards of care. This study may also reveal associations that are possibly good targets for public health intervention. This is especially important in our country as there is a locally observed predisposition to injury for hard labour and construction workers, so there it is necessity to see if there is an association between current working conditions and likeliness of injury.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ankle Fractures, Splints

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
100 (Actual)

8. Arms, Groups, and Interventions

Arm Title
post operative Ankle fractures with splint
Arm Type
Active Comparator
Arm Description
All patient who meet the inclusion criteria of having ankle fracture that rigidly fixed and randomized to receive splint post operative
Arm Title
post operative Ankle fractures without splint
Arm Type
No Intervention
Arm Description
All patient who meet the inclusion criteria of having ankle fracture that rigidly fixed and randomized to receive NO splint post operative
Intervention Type
Procedure
Intervention Name(s)
Splinting (plaster of paris)
Intervention Description
Placing stockinette followed by cotton rolls and 10-12 layer of posterior ankle splint made of plaster of paris
Primary Outcome Measure Information:
Title
Assessing the change in the level of pain between the splint and no-splint groups
Description
Visual analogue scale (0;lowest pain, 10;highest pain)
Time Frame
Change in pain from 2 weeks postop to 1 year postop
Title
Assessing the change in ankle swelling from 2 weeks postop to 1 year postop in the splint and no-splint groups
Description
Measuring tape to assess supramalleolar, mid-foot, and mid-calf circumference
Time Frame
Change in swelling from 2 weeks postop to 1 year postop
Secondary Outcome Measure Information:
Title
Change in the functional scoring system used below
Description
The American Orthopaedic Foot and Ankle Society (AOFAS) Ankle-Hindfoot Score
Time Frame
Change in American Orthopaedic Foot and Ankle Society (AOFAS) Ankle-Hindfoot Scorefrom 2 weeks postop to 1 year postop
Title
Number of participants with; infection, nonunion, deep-vein thrombosis, stiffness, equinus
Description
Rate of infection, nonunion, deep-vein thrombosis, stiffness, equinus
Time Frame
From 2 weeks postop - 1 year postop

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: A.O 44 ankle fractures requiring surgical fixation (uni or bimalleolar with /without syndesmotic injury) Exclusion Criteria: pathological fracture poly trauma pilon fractures open fractures other associated fractures in same extremity peripheral neuropathy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ali Jarragh, MD
Organizational Affiliation
Kuwait University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mubarak Al kabeer hospital
City
Kuwait
Country
Kuwait

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
7822349
Citation
Michelson JD. Fractures about the ankle. J Bone Joint Surg Am. 1995 Jan;77(1):142-52. doi: 10.2106/00004623-199501000-00020. No abstract available.
Results Reference
background
PubMed Identifier
3132812
Citation
Ahl T, Dalen N, Selvik G. Mobilization after operation of ankle fractures. Good results of early motion and weight bearing. Acta Orthop Scand. 1988 Jun;59(3):302-6. doi: 10.3109/17453678809149368.
Results Reference
background
PubMed Identifier
3425285
Citation
Daly PJ, Fitzgerald RH Jr, Melton LJ, Ilstrup DM. Epidemiology of ankle fractures in Rochester, Minnesota. Acta Orthop Scand. 1987 Oct;58(5):539-44. doi: 10.3109/17453678709146395.
Results Reference
background
PubMed Identifier
11792591
Citation
Valtola A, Honkanen R, Kroger H, Tuppurainen M, Saarikoski S, Alhava E. Lifestyle and other factors predict ankle fractures in perimenopausal women: a population-based prospective cohort study. Bone. 2002 Jan;30(1):238-42. doi: 10.1016/s8756-3282(01)00649-4.
Results Reference
background
PubMed Identifier
9692074
Citation
Honkanen R, Tuppurainen M, Kroger H, Alhava E, Saarikoski S. Relationships between risk factors and fractures differ by type of fracture: a population-based study of 12,192 perimenopausal women. Osteoporos Int. 1998;8(1):25-31. doi: 10.1007/s001980050044.
Results Reference
background
PubMed Identifier
25695796
Citation
Smeeing DP, Houwert RM, Briet JP, Kelder JC, Segers MJ, Verleisdonk EJ, Leenen LP, Hietbrink F. Weight-bearing and mobilization in the postoperative care of ankle fractures: a systematic review and meta-analysis of randomized controlled trials and cohort studies. PLoS One. 2015 Feb 19;10(2):e0118320. doi: 10.1371/journal.pone.0118320. eCollection 2015.
Results Reference
background
PubMed Identifier
23152232
Citation
Lin CW, Donkers NA, Refshauge KM, Beckenkamp PR, Khera K, Moseley AM. Rehabilitation for ankle fractures in adults. Cochrane Database Syst Rev. 2012 Nov 14;11:CD005595. doi: 10.1002/14651858.CD005595.pub3.
Results Reference
result

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Post Operative Ankle Splint Study - Prospective Multi Center Randomized Controlled Trial

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