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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03945669
Other study ID # LERG1
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date November 1, 2019
Est. completion date August 1, 2025

Study information

Verified date June 2023
Source Aalborg University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study is a multicenter pragmatic assessor blinded randomized and prospective clinical trial in which standard intramedullary nailing is compared with external ring fixator for patients with tibial shaft fractures.


Description:

This study is a multicenter pragmatic assessor blinded randomized and prospective clinical trial in which standard intramedullary nailing is compared with external ring fixator for patients with tibial shaft fractures. The primary aim of the project is to compare the one-year Knee Injury and Osteoarthritis Outcome Score - Sport (KOOS-Sport) after standard intramedullary nailing with external ring fixation for patients with tibial shaft fractures. The explorative aim is to report the effect of the two surgical procedures on the development of complications, time to bone union, pain reactions, muscle strength, activity of daily living and time to return to work.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 67
Est. completion date August 1, 2025
Est. primary completion date June 1, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Fracture of the tibial shaft - OTA classification Type: 42-A1-A3, -B1-B3 and -C1-C3 - The fracture type is deemed operable by intramedullary nail Exclusion Criteria: - Below 18 years of age - Open fracture - History of severe systemic diseases or cancer - Bilateral tibial shaft fracture - Multi fracture patients - Pregnancy - Patients without gait function prior to fracture

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Intramedullary Nailing
fracture fixation of the tibial shaft fracture with an intramedullary nail.
External Ring fixation
fracture fixation of the tibial shaft fracture with an external ring fixator.

Locations

Country Name City State
Denmark Aalborg University Hospital, Department of orthopaedic surgery Aalborg
Denmark Aarhus University Hospital Aarhus
Denmark Regional Hospital Viborg Viborg

Sponsors (2)

Lead Sponsor Collaborator
Aalborg University Hospital Danish Council for Independent Research

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Other Adverse events Adverse events, defined as any negative or unwanted reactions to the two surgical procedures, will be recorded. These will include deep infection, pin infection, skin infections, malalignment, compartment syndrome or any other reported physical discomfort. An adverse effects committee will manage adverse reactions at the time of the adverse reaction. 6 weeks, 3+6+12 months
Primary The Knee Injury and Osteoarthritis Outcome Score - sport (KOOS Sport) KOOS-sport is a standardized and validated patient-reported instrument used in order to assess knee and knee associated problems with regards to activity. The subscale sport is one five subscales: pain, ADL, symptoms, sport and QOL in the KOOS questionnaire . A total score of 100 indicates no symptoms, and 0 indicates major symptoms. 12 month follow up
Secondary Perceived Pain Development in pain in the two groups will be recorded by patient-reported pain intensity measured on a 10 cm visual analogue scale (VAS) with endpoints "no pain" and "maximal pain" for the worst pain during the last 24 hours and resting pain. 6 weeks, 3+6+12 months
Secondary Patient-reported pain reactions Pain DETECT questionnaire. The painDETECT screening questionnaire (PD-Q), uses a scoring method between - 1 and 38 to estimate the likelihood of a neuropathic pain component in patients. 6 weeks, 3+6+12 months
Secondary Pain sensitivity Pain sensitivity will be assessed by pressure pain thresholds (PPTs) recorded by handheld pressure algometry (Algometer Type II, Somedic AB, Sweden). 6 weeks, 3+6+12 months
Secondary Muscle strength Isometric muscle strength in the two groups will be measured by a strap-mounted dynamometer attached to the wall (Mecmesin AFG2500, Mecmesin Ltd, West Sussex, UK). Girth measures of thigh and calf will be used to examine muscle atrophy and/or effusion 6+12 months
Secondary Time to bone union Bone union, in the two surgical groups will be evaluated on standard AP and side X-rays of the fractured leg. The evaluation of bone union will be defined as: i) visible callus formation on at least three of four sides, no visible fracture line and no pain from fracture site at weight-bearing and during clinical examination. 6 weeks, 3+6+12 months
Secondary Radiological alignment Alignment of the tibia will be evaluated using the EOS scanning system. 6 weeks, 3+6+12 months
Secondary Health related QOL Eq5D-5L is a standardized questionnaire developed to assess general health outcome (29). It consists of five dimensions: Mobility, self-care, usual activities, pain/discomfort and anxiety/depression, and a self-rated health scale on a 20 cm vertical, visual analogue scale with endpoints labelled 'the best health you can imagine' and 'the worst health you can imagine'. An Eq5d-5L index of 1.0 indicated full health, 0 death, and -0.59 denoted a condition worse than death 6 weeks, 3+6+12 months
Secondary Time to return to work Measure the time from surgery to end of sick leave measured in days. 6 weeks, 3+6+12 months
Secondary Health economic evaluation Measure the cost of treatment in the two groups within the first year following surgery 12 months
Secondary Gait assessment Gait asymmetries will be measured with patients walking on a pressure-sensitive mat. 3+6+12 months
Secondary Patient Acceptable Symptom State (PASS) This instrument evaluate when the patient reaches a acceptable patient observed pain and function level, where the patient no longer demands treatment 3+6+12 months
Secondary The Knee Injury and Osteoarthritis Outcome Score (KOOS) KOOS is a standardized and validated patient-reported instrument used in order to assess knee and knee associated problems.The questionnaire includes five subscales: pain, ADL, symptoms, sport and QOL. A total score of 100 indicates no symptoms, and 0 indicates major symptoms. 6 weeks, 3+6+12 months
Secondary Foot And Ankle Outcome Score (FAOS) FAOS is a standardized and validated patient-reported instrument used in order to assess foot and ankle associated problems divided into 5 subscales. The questionnaire includes five subscales: pain, ADL, symptoms, sport and QOL. A total score of 100 indicates no symptoms, and 0 indicates major symptoms. 6 weeks, 3+6+12 months
See also
  Status Clinical Trial Phase
Completed NCT01190709 - Study of Tibial Shaft Fracture Fixation: Intramedullary Nailing Comparing With Dynamic Compression Plate Phase 2
Enrolling by invitation NCT05521958 - Gene Expression in Lower Extremity Acute Traumatic Compartment Syndrome N/A
Not yet recruiting NCT05627479 - MAGIK for Femoral/Tibial Shaft Fractures Phase 2