Os Calcis FractureNCT01615744
Surgical vs Conservative Treatment of Displaced Intra-articular Calcaneal Fractures: A Prospective RCT
An observational study of Os Calcis Fracture, run by Agren, Per-Henrik, M.D. at 1 site in Sweden.
Trial summary
Between 1994-98 5 hospitals in Stockholm investigated calcaneal fractures in a randomised study. 82 patients were included and randomized either to non-surgical treatment or surgical management with extensile lateral approach and reduction with Internal fixation (ORIF) The patients were followed and investigated at… Read more about this study
- Who is it for?
- Ages 18 to 78 years
- Conditions the study is for
- Os Calcis Fracture
- What is being tested?
- Open Reduction Internal Fixation and Non-surgical management
- Type of treatment
- Surgery or procedure
- How many people
- 82 participants
- Where
- 1 siteSweden
- Study dates
- Dec 1993to Dec 1998
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 78 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Between 1994 and 1998. Patients presenting at 5 hospitals in Stockholm after trauma resulting in a fracture with > 2mm Dislocated Intraarticular Calcaneal Fractures (DIACFs) verified by axial and coronal computerized tomography (CT) scan were considered for inclusion
Who may be able to join
- Patients presented with > 2mm DIACFs verified by axial and coronal computerized tomography (CT) scan were considered for inclusion
Who cannot join
- Peripheral neuro-vascular disease (signs and symptoms of ischemia or neuropathy), open fractures, uncontrolled diabetes mellitus and medical contra-indications to surgery.
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Surgical vs. Conservative Treatment of Displaced Intra-articular Calcaneal Fractures: A Prospective, Randomized, Controlled Multicenter Trial
Between 1994-98 5 hospitals in Stockholm investigated calcaneal fractures in a randomised study.
82 patients were included and randomized either to non-surgical treatment or surgical management with extensile lateral approach and reduction with Internal fixation (ORIF) The patients were followed and investigated at fixed intervals 2 weeks, 8 weeks, 3 months and 6 months for clinical review. At 1 year and 8-12 years (mean 10 years) post-injury.
Both clinical radiological data were collected and several scores were used. The primary outcomes scores used were SF-36 and VAS score.
The results after 1 year and mean 10 years are presented.
Read the detailed description
The study was approved by the local ethical committee. Seven trauma orthopaedic surgeons in five hospitals in Stockholm were recruited in this RCT, which was conducted between 1994 and 1998. Patients presented with > 2mm DIACFs verified by axial and coronal computerized tomography (CT) scan were considered for inclusion. Exclusion criteria included peripheral neuro-vascular disease (signs and symptoms of ischemia or neuropathy), open fractures, uncontrolled diabetes mellitus and medical contra-indications to surgery.
All centers used the same study protocol. Demographic data were obtained from the patients, as they deemed eligible to participate in the study. Informed consent was obtained from each patient. Randomization was carried out by sealed opaque envelope to choose surgical vs. conservative treatment.
The surgical treatment was carried out within 2 weeks post-injury when the local soft tissue swelling subsided. Surgery included open reduction using the lateral extensile approach according to Benirschke (ref) and manipulation of the fragments as described by Soeur and Remy (ref) to achieve anatomical reduction, which then was fixed by screws, reconstruction plates or calcaneal plates. Using bone grafts was left to the judgment of the surgeon. Postoperatively, plain X-ray and CT scan were used to evaluate the quality of fracture reduction. Sex week's non-weight bearing was advocated for all patients. Range-of-motion exercises were allowed during this period. Thereafter, the patients had a standardized physiotherapy regimen with full weight bearing.
The conservative treatment included rest, elevation and non-weight bearing. Early range-of-motion exercises were encouraged as tolerated. After 6-8 weeks weight bearing was allowed and shoe modification was provided to those who had hind foot deformities.
No patients were managed with impulse compression therapy.
Patients of both groups were followed-up by treating surgeons at 2 weeks, 8 weeks, 3 months and 6 months for clinical review. At 1 year and 8-12 years (mean 10 years) post-injury, all patients were evaluated by unbiased surgeons who were not involved in the treatment of the patients and they completed the following questionnaires:
- Primary outcome measures: visual analogue scale (VAS) scoring devised and tested by Hildebrand et al (ref) and a self-administrated general health outcome form (SF-36) for physical and mental health.
- Secondary outcome measures: VAS at rest and on weight bearing (0-10), the American Orthopaedic Foot \& Ankle Society (AOFAS) hindfoot scale and the Olerud-Molander (OM) score.
The investigators divided each group into two subgroups, younger and older than 50 years to determine if the results of the outcome measures at 1 year would differ according to the age of the patients.
During controls, clinical evaluation was carried out to measure the ankle joint and subtalar joint range of motion and the length and width of the hind foot. The contra-lateral non-fractured foot was used for comparison. Shoe problems, the outcome of any eventual postoperative/post-injury complications and workers´ compensation were documented. Radiological follow-up with axial and coronal CT scan was done at the 1 year and 3 years visits.
Statistical analysis The SPSS program version 18.0 for personal computers (Chicago, Illinois) was used for data analysis. The variables of interests were analyzed to determine the differences using bivariate comparisons. The means with standard deviation (SD) were measured. The Mann-Whitney test was used for non-parametric data while two-sample t-test was used for parametric data. A p value of <0.05 was considered significant.
- Conditions
- Os Calcis Fracture
- Being tested
- Open Reduction Internal Fixation, Non-surgical management
- Keywords
- calcaneal fractures, surgical treatment, conservative treatment, VAS scoring, SF-36, AOFAS, Olerud-Molander score, outcome
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Open Reduction Internal FixationProcedure or surgery
Also called Surgery
Lateral approach through extensile lateral incision ( Benirschke), Reduction ( Soeur et Remy) and internal fixation with lateral plating with or without bone graft
Non-surgical managementProcedure or surgery
Also called No surgery, early movement, decreasing swelling
Early active exercises and elevation to decrease swelling
| Study group | Role | What they receive |
|---|---|---|
| Surgical ORIF calcaneal fx | Not described Receives: Procedure: Open Reduction Internal Fixation | |
| Conservative treatment calcaneal fx | Not described Receives: Procedure: Non-surgical management |
What is being measured
The primary outcome is the main question the study is designed to answer.
SF-36
The investigators anticipate that there might be a change over time and want to investigate and describe it
Measured: 1 year and 10 years post injury
VAS-score (calcaneal fractures) /Hildebrand, Buckley
The investigators anticipate that there might be a change over time and want to investigate and describe it
Measured: 1 year and 10 years post injury
Secondary outcomes (3)
VAS of pain at rest and exertion
The investigators anticipate that there might be a change over time and want to investigate and describe it
Measured: 2 weeks,6 weeks,12 weeks,1 year, 3 years and 10 years post injury
AOFAS hindfoot scale
The investigators anticipate that there might be a change over time and want to investigate and describe it
Measured: 1 year and 10 years post injury
Olerud-Molander score
The investigators anticipate that there might be a change over time and want to investigate and describe it
Measured: 1 year and 10 years post injury
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted11 Jun 2012 (estimated)
- Study startDec 1993
- Primary completionJan 1994
- Study completionDec 1998
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Os Calcis FractureStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Case-control
- Time perspective
- Prospective
- Enrolment
- 82 participants (actual)
Sponsor and investigators
- Lead sponsor
- Agren, Per-Henrik, M.D.
- Responsible party
- Sponsor
- Investigators
- Per-Henrik Aagren, MD, Principal investigator, Consultant Orthopaedic Surgeon
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01615744
- Sponsor's protocol ID
- CalcanealfxRCT
- Status last verified
- Jun 2012
- First submitted
- 5 Jun 2012
- Last updated
- 11 Jun 2012
- Results posted
- No
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 11 Jun 2012. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Surgical vs. Conservative Treatment of Displaced Intra-articular Calcaneal Fractures: A Prospective, Randomized, Controlled Multicenter Trial
- ClinicalTrials.gov ID
- NCT01615744
- Acronym / sponsor ID
- CalcanealfxRCT
- Conditions
- Os Calcis Fracture
- Keywords
- calcaneal fractures, surgical treatment, conservative treatment, VAS scoring, SF-36, AOFAS, Olerud-Molander score, outcome
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 82 participants (actual)
- Lead sponsor
- Agren, Per-Henrik, M.D.
- Study start
- Dec 1993
- Primary completion
- Jan 1994 (actual)
- Study completion
- Dec 1998 (actual)
- First posted
- 11 Jun 2012 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Between 1994-98 5 hospitals in Stockholm investigated calcaneal fractures in a randomised study.
82 patients were included and randomized either to non-surgical treatment or surgical management with extensile lateral approach and reduction with Internal fixation (ORIF) The patients were followed and investigated at fixed intervals 2 weeks, 8 weeks, 3 months and 6 months for clinical review. At 1 year and 8-12 years (mean 10 years) post-injury.
Both clinical radiological data were collected and several scores were used. The primary outcomes scores used were SF-36 and VAS score.
The results after 1 year and mean 10 years are presented.
Detailed description
The study was approved by the local ethical committee. Seven trauma orthopaedic surgeons in five hospitals in Stockholm were recruited in this RCT, which was conducted between 1994 and 1998. Patients presented with > 2mm DIACFs verified by axial and coronal computerized tomography (CT) scan were considered for inclusion. Exclusion criteria included peripheral neuro-vascular disease (signs and symptoms of ischemia or neuropathy), open fractures, uncontrolled diabetes mellitus and medical contra-indications to surgery.
All centers used the same study protocol. Demographic data were obtained from the patients, as they deemed eligible to participate in the study. Informed consent was obtained from each patient. Randomization was carried out by sealed opaque envelope to choose surgical vs. conservative treatment.
The surgical treatment was carried out within 2 weeks post-injury when the local soft tissue swelling subsided. Surgery included open reduction using the lateral extensile approach according to Benirschke (ref) and manipulation of the fragments as described by Soeur and Remy (ref) to achieve anatomical reduction, which then was fixed by screws, reconstruction plates or calcaneal plates. Using bone grafts was left to the judgment of the surgeon. Postoperatively, plain X-ray and CT scan were used to evaluate the quality of fracture reduction. Sex week's non-weight bearing was advocated for all patients. Range-of-motion exercises were allowed during this period. Thereafter, the patients had a standardized physiotherapy regimen with full weight bearing.
The conservative treatment included rest, elevation and non-weight bearing. Early range-of-motion exercises were encouraged as tolerated. After 6-8 weeks weight bearing was allowed and shoe modification was provided to those who had hind foot deformities.
No patients were managed with impulse compression therapy.
Patients of both groups were followed-up by treating surgeons at 2 weeks, 8 weeks, 3 months and 6 months for clinical review. At 1 year and 8-12 years (mean 10 years) post-injury, all patients were evaluated by unbiased surgeons who were not involved in the treatment of the patients and they completed the following questionnaires:
- Primary outcome measures: visual analogue scale (VAS) scoring devised and tested by Hildebrand et al (ref) and a self-administrated general health outcome form (SF-36) for physical and mental health.
- Secondary outcome measures: VAS at rest and on weight bearing (0-10), the American Orthopaedic Foot \& Ankle Society (AOFAS) hindfoot scale and the Olerud-Molander (OM) score.
The investigators divided each group into two subgroups, younger and older than 50 years to determine if the results of the outcome measures at 1 year would differ according to the age of the patients.
During controls, clinical evaluation was carried out to measure the ankle joint and subtalar joint range of motion and the length and width of the hind foot. The contra-lateral non-fractured foot was used for comparison. Shoe problems, the outcome of any eventual postoperative/post-injury complications and workers´ compensation were documented. Radiological follow-up with axial and coronal CT scan was done at the 1 year and 3 years visits.
Statistical analysis The SPSS program version 18.0 for personal computers (Chicago, Illinois) was used for data analysis. The variables of interests were analyzed to determine the differences using bivariate comparisons. The means with standard deviation (SD) were measured. The Mann-Whitney test was used for non-parametric data while two-sample t-test was used for parametric data. A p value of <0.05 was considered significant.
Study design
- Observational model
- Case-control
- Time perspective
- Prospective
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Surgical ORIF calcaneal fx | – | Procedure: Open Reduction Internal Fixation |
| Conservative treatment calcaneal fx | – | Procedure: Non-surgical management |
Who may qualify
- Ages
- 18 to 78 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Between 1994 and 1998. Patients presenting at 5 hospitals in Stockholm after trauma resulting in a fracture with > 2mm Dislocated Intraarticular Calcaneal Fractures (DIACFs) verified by axial and coronal computerized tomography (CT) scan were considered for inclusion
Key inclusion criteria (1 listed)
- Patients presented with > 2mm DIACFs verified by axial and coronal computerized tomography (CT) scan were considered for inclusion
Key exclusion criteria (1 listed)
- Peripheral neuro-vascular disease (signs and symptoms of ischemia or neuropathy), open fractures, uncontrolled diabetes mellitus and medical contra-indications to surgery.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Open Reduction Internal FixationAlso: SurgeryLateral approach through extensile lateral incision ( Benirschke), Reduction ( Soeur et Remy) and internal fixation with lateral plating with or without bone graft | Procedure or surgery | Surgical ORIF calcaneal fx |
| Non-surgical managementAlso: No surgery, early movement, decreasing swellingEarly active exercises and elevation to decrease swelling | Procedure or surgery | Conservative treatment calcaneal fx |
Primary outcome
SF-36
Time frame: 1 year and 10 years post injury
The investigators anticipate that there might be a change over time and want to investigate and describe it
VAS-score (calcaneal fractures) /Hildebrand, Buckley
Time frame: 1 year and 10 years post injury
The investigators anticipate that there might be a change over time and want to investigate and describe it
3 secondary outcomes
VAS of pain at rest and exertion
Time frame: 2 weeks,6 weeks,12 weeks,1 year, 3 years and 10 years post injury
AOFAS hindfoot scale
Time frame: 1 year and 10 years post injury
Olerud-Molander score
Time frame: 1 year and 10 years post injury
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 11 Jun 2012.
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Per-Henrik Aagren, MD principal investigator
Consultant Orthopaedic Surgeon
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Os Calcis Fracture, run by Agren, Per-Henrik, M.D. at 1 site in Sweden.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 11 Jun 2012. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Sweden. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
SF-36 (time frame: 1 year and 10 years post injury). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Jun 2012; AzTrials last refreshed its copy on 8 Nov 2026.