- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06372067
IM Screw vs. K-wire Fixation of Proximal/Middle Phalanx Fractures (HANDFIX)
Intramedullary Screw Versus Kirschner Wire Fixation of Extraarticular Proximal and Middle Phalanx Fractures: Pilot Study for a Randomized Controlled Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Hand fractures are one of the most common skeletal injuries and affect a wide range of the population. Commonly affected groups include children and young adults with sports-related injuries, manual labourers with work-related injuries, and the elderly. Although the majority of phalanx fractures may be managed conservatively with good outcomes, operative fixation is indicated for significantly displaced or unstable fracture patterns, and those causing malrotation and scissoring.
There are a variety of options for operative fixation of proximal and middle phalanx fractures, which include closed versus open reduction (CR vs OR) with percutaneous pinning (PP) or internal fixation (IF) techniques. Kirschner wires (K-wire) and plates/screws are the most common CRPP and ORIF techniques. K-wires allow for fracture fixation with minimal soft tissue injury and preserved blood supply. However, patients require prolonged postoperative immobilization and are at risk of malunion and pin tract infection. Conversely, ORIF with plates/screws provide rigid fixation allowing for early mobilization, but require opening of fracture site and often periosteal stripping. Complications with ORIF include adhesions and stiffness.
There is emerging evidence for the effectiveness of intramedullary (IM) screw fixation as an alternative technique for IF. IM screw fixation is a minimally invasive technique that provides rigid fixation of fractures, acting as an internal splint and load-sharing device. Its biomechanical properties have been well-described in the lower extremity orthopedic literature. IM screw fixation may allow for early mobilization without the operative site morbidity of open reduction and its associated complications. Small observational cohort studies have shown favourable outcomes in return to activity, range of motion, time to radiological healing, and grip strength. However, the investigators' literature search revealed a paucity of high quality studies comparing the effectiveness of IM screws with K-wires or other methods of fixation.
The primary objective of this pilot study is to assess the feasibility of a randomized controlled trial comparing two CR techniques, i.e. IM screw fixation to K-wire fixation, in adult patients with extraarticular proximal or middle phalanx fracture at the investigators' tertiary academic hospital. The secondary objective will be to describe early clinical outcomes which can be used for future trial sample size calculation.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Ontario
-
Hamilton, Ontario, Canada, l6l5n4
- Recruiting
- St. Joseph's Healthcare
-
Contact:
- Emily Dunn, MSc
- Phone Number: 905-522-1155
- Email: dunne4@mcmaster.ca
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- adult patients ≥18 years old
- scheduled for operative management of extraarticular proximal or middle closed phalanx fracture(s) at the investigators' tertiary hospital
- feasible to perform closed reduction
- able to provide informed consent and complete health-related quality of life (HRQoL) questionnaires in English
Exclusion Criteria:
- other fractures that cannot be managed with IM screws or K-wires
- other intraarticular fractures
- significant concomitant hand trauma
- cannot commit to 3 months of follow up at the investigators' institution
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intramedullary screw
Intramedullary (IM) screw fixation is a minimally invasive technique that provides rigid fixation of fractures, acting as an internal splint and load-sharing device.
IM screw fixation may allow for early mobilization without the operative site morbidity of open reduction and its associated complications.
|
Intramedullary (IM) screw fixation is a minimally invasive technique that provides rigid fixation of fractures, acting as an internal splint and load-sharing device.
IM screw fixation may allow for early mobilization without the operative site morbidity of open reduction and its associated complications.
|
|
Active Comparator: Kirschner wire
Kirschner wire (K-wire) fixation is a minimally invasive technique that provides non-rigid fixation of fractures.
K-wires allow for fracture fixation with minimal soft tissue injury and preserved blood supply.
However, patients require prolonged postoperative immobilization and are at risk of malunion and pin tract infection.
|
Kirschner wire (K-wire) fixation is a minimally invasive technique that provides non-rigid fixation of fractures.
K-wires allow for fracture fixation with minimal soft tissue injury and preserved blood supply.
However, patients require prolonged postoperative immobilization and are at risk of malunion and pin tract infection.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Percentage of Patient Eligibility - Study Feasibility
Time Frame: 1 year
|
The percentage of patients that are eligible for the study among those that are screened will be recorded.
This criteria will be determined to be feasible if at least 70% of screened patients are deemed to be eligible.
|
1 year
|
|
Recruitment rate - Study Feasibility
Time Frame: 1 year
|
The percentage of patients that are enrolled in the study among those determined to be eligible will be recorded.
To be considered fully enrolled patients must sign the informed consent form, complete baseline demographic questionnaires, and be randomized to a study arm.
This criteria will be determined to be feasible if at least 70% of eligible patients are recruited.
|
1 year
|
|
Crossover rate - Study Feasibility
Time Frame: 1 year
|
The percentage of patients that crossover to the other arm of the study among those who are eligible and recruited for the study.
This criteria will be determined to be feasible if no more than 5% of patients cross over.
|
1 year
|
|
Compliance with intervention rate - Study Feasibility
Time Frame: 1 year
|
The percentage of patients that comply with the intervention (appropriate post-operative care, follow-up appointments) among those who are eligible and recruited for the study.
This criteria will be determined to be feasible if at least 90% of patients are compliant.
|
1 year
|
|
Patient retention rate - Study Feasibility
Time Frame: 1 year
|
The percentage of patients that complete patient-reported questionnaire (Disabilities of the Arm, Shoulder, and Hand) at the 3-month mark, which will be the primary outcome of the main trial.
Scores range from 0-100 points, where higher scores indicate greater disability.
This criteria will be determined to be feasible if at least 80% of patients are compliant.
|
1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Disability of the Arm, Shoulder, and Hand
Time Frame: baseline, 4 weeks, 12 weeks
|
The Disability of the Arm, Shoulder, and Hand is a region-specific PROM that has been shown to be valid, reliable, and responsive to change in measuring patient-important domains pertaining to the upper extremity.
Scores range from 0-100 points, where higher scores indicate greater disability.
In trauma populations, the Disability of the Arm, Shoulder, and Hand has been shown to have excellent internal consistency (0.98) and test-retest probability (intraclass correlation coefficient [ICC] = 0.98).
The Disability of the Arm, Shoulder, and Hand has also been reported to have good criterion validity, construct validity and responsiveness in hand trauma patients.
|
baseline, 4 weeks, 12 weeks
|
|
Range of motion
Time Frame: 4 weeks, 8 weeks, 12 weeks
|
Range of motion of the affected finger, compared to the contralateral finger.
As measured and reported by hand therapist appointments which are part of routine care at the investigators' institution.
|
4 weeks, 8 weeks, 12 weeks
|
|
Grip strength
Time Frame: 8 weeks, 12 weeks
|
Grip strength of the affected hand, compared to the contralateral hand.
As measured and reported by hand therapist appointments which are part of routine care at the investigators' institution.
|
8 weeks, 12 weeks
|
|
Return to work
Time Frame: through study completion, an average of 3 months
|
Time of patient-reported return to work or surgeon clearance for return to work.
|
through study completion, an average of 3 months
|
|
Complications/adverse events
Time Frame: 2 weeks, 4 weeks, 8 weeks, 12 weeks
|
Post-operative complications/adverse events include but are not limited to stiffness, delayed union, non-union, malunion, infection, hardware removal, reoperation.
|
2 weeks, 4 weeks, 8 weeks, 12 weeks
|
|
Postoperative pain (visual analogue scale)
Time Frame: 2 weeks, 4 weeks, 8 weeks, 12 weeks
|
Pain will be measured postoperative on the visual analogue scale, which ranges from 0-10.
Higher scores indicate greater pain.
|
2 weeks, 4 weeks, 8 weeks, 12 weeks
|
Collaborators and Investigators
Sponsor
Publications and helpful links
General Publications
- Thabane L, Ma J, Chu R, Cheng J, Ismaila A, Rios LP, Robson R, Thabane M, Giangregorio L, Goldsmith CH. A tutorial on pilot studies: the what, why and how. BMC Med Res Methodol. 2010 Jan 6;10:1. doi: 10.1186/1471-2288-10-1.
- Gummesson C, Atroshi I, Ekdahl C. The disabilities of the arm, shoulder and hand (DASH) outcome questionnaire: longitudinal construct validity and measuring self-rated health change after surgery. BMC Musculoskelet Disord. 2003 Jun 16;4:11. doi: 10.1186/1471-2474-4-11. Epub 2003 Jun 16.
- Eldridge SM, Chan CL, Campbell MJ, Bond CM, Hopewell S, Thabane L, Lancaster GA; PAFS consensus group. CONSORT 2010 statement: extension to randomised pilot and feasibility trials. BMJ. 2016 Oct 24;355:i5239. doi: 10.1136/bmj.i5239.
- Beaton DE, Katz JN, Fossel AH, Wright JG, Tarasuk V, Bombardier C. Measuring the whole or the parts? Validity, reliability, and responsiveness of the Disabilities of the Arm, Shoulder and Hand outcome measure in different regions of the upper extremity. J Hand Ther. 2001 Apr-Jun;14(2):128-46.
- Meals C, Meals R. Hand fractures: a review of current treatment strategies. J Hand Surg Am. 2013 May;38(5):1021-31; quiz 1031. doi: 10.1016/j.jhsa.2013.02.017.
- Kremer L, Frank J, Lustenberger T, Marzi I, Sander AL. Epidemiology and treatment of phalangeal fractures: conservative treatment is the predominant therapeutic concept. Eur J Trauma Emerg Surg. 2022 Feb;48(1):567-571. doi: 10.1007/s00068-020-01397-y. Epub 2020 May 25.
- Chao J, Patel A, Shah A. Intramedullary Screw Fixation Comprehensive Technique Guide for Metacarpal and Phalanx Fractures: Pearls and Pitfalls. Plast Reconstr Surg Glob Open. 2021 Oct 26;9(10):e3895. doi: 10.1097/GOX.0000000000003895. eCollection 2021 Oct.
- Bong MR, Kummer FJ, Koval KJ, Egol KA. Intramedullary nailing of the lower extremity: biomechanics and biology. J Am Acad Orthop Surg. 2007 Feb;15(2):97-106. doi: 10.5435/00124635-200702000-00004.
- del Pinal F, Moraleda E, Ruas JS, de Piero GH, Cerezal L. Minimally invasive fixation of fractures of the phalanges and metacarpals with intramedullary cannulated headless compression screws. J Hand Surg Am. 2015 Apr;40(4):692-700. doi: 10.1016/j.jhsa.2014.11.023. Epub 2015 Feb 7.
- Patankar H, Meman FW. Multiple intramedullary nailing of proximal phalangeal fractures of hand. Indian J Orthop. 2008 Jul;42(3):342-6. doi: 10.4103/0019-5413.39573.
- Verver D, Timmermans L, Klaassen RA, van der Vlies CH, Vos DI, Schep NWL. Treatment of extra-articular proximal and middle phalangeal fractures of the hand: a systematic review. Strategies Trauma Limb Reconstr. 2017 Aug;12(2):63-76. doi: 10.1007/s11751-017-0279-5. Epub 2017 Mar 4.
- Deshmukh SR, Mousoulis C, Marson BA, Grindlay D, Karantana A; Core Outcome Set for Hand Fractures and Joint Injuries in Adults Group*. Developing a core outcome set for hand fractures and joint injuries in adults: a systematic review. J Hand Surg Eur Vol. 2021 Jan 24:1753193420983719. doi: 10.1177/1753193420983719. Online ahead of print.
- Ziebart C, Bobos P, Furtado R, Dabbagh A, MacDermid J. Patient-reported outcome measures used for hand and wrist disorders: An overview of systematic reviews. J Hand Ther. 2023 Jul-Sep;36(3):719-729. doi: 10.1016/j.jht.2022.10.007. Epub 2023 Mar 11.
- Esteban-Feliu I, Gallardo-Calero I, Barrera-Ochoa S, Lluch-Bergada A, Alabau-Rodriguez S, Mir-Bullo X. Analysis of 3 Different Operative Techniques for Extra-articular Fractures of the Phalanges and Metacarpals. Hand (N Y). 2021 Sep;16(5):595-603. doi: 10.1177/1558944719873144. Epub 2019 Sep 13.
- Gaio NM, Kruse LM. Closed Reduction Percutaneous Pinning Versus Open Reduction With Plate and Screw Fixation in Management of Unstable Proximal Phalangeal Fractures: A Systematic Review and Meta-analysis. Hand (N Y). 2025 Jan;20(1):136-142. doi: 10.1177/15589447231189762. Epub 2023 Aug 20.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 17378
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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