Ankle OsteoarthritisNCT03772236
Phi Angle and Antero-medial Pain in Total Ankle Replacement Follow-up
An observational study of Ankle Osteoarthritis and Prostheses and Implants, run by I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio at 1 site in Italy.
Trial summary
The study evaluates the relation between the rotational alignment of the talar component (phi angle) and the antero-medial ankle pain in patients underwent total ankle replacement, at least one year after surgery. Read more about this study
- Who is it for?
- Ages 18 to 60 years
- Conditions the study is for
- Ankle Osteoarthritis, Prostheses and Implants
- How many people
- 100 participants
- Where
- 1 siteItaly
- Study dates
- 4 Dec 2018to 30 Jun 2020
- 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 60 years
- All sexes
- No healthy volunteers
- Adult
Study population: Patients undergoing follow-up examination at a third-level hospital after total ankle replacement
Who may be able to join
- previous intervention of first implant of total ankle replacement, with at least 12 months of follow up and maximum 36 months
Who cannot join
- more than 36 months from the surgery of first implant of total ankle replacement
- previous revision surgery of ankle prosthesis
- previous intervention of ankle disarthrodesis and ankle prosthesis implant
Trial locations and contacts
1 site in 1 country.
Italy1 site, 1 recruiting
- Recruiting
Irccs Istituto Ortopedico Galeazzi
Milan, Milano, 20156
Federico Usuelli, MD, +393357351838, fusuelli@gmail.com
Federico Usuelli, MD
About this study
Official title: Evaluation of the Relation Between the Rotation Angle of the Talar Component and the Antero-medial Pain in Patients Underwent Total Ankle Replacement, at Least One Year After Surgery
The study evaluates the relation between the rotational alignment of the talar component (phi angle) and the antero-medial ankle pain in patients underwent total ankle replacement, at least one year after surgery.
Moreover, the study aims to define a range of the phi angle associated with a lower frequency of antero-medial pain.
Read the detailed description
Background:
In case of total ankle prosthesis surgery, the correct positioning of the talar component is one of the most challenging tasks. When performing total ankle replacement, the primary goal for long-term implant survival is to restore a physiological alignment of the prosthesis in the lateral and frontal planes. In fact, an incorrect alignment can alter joint mechanics and joint reactive forces that can lead to implant failure (Saltzman, 2004).
Regarding the rotation in the dorsoplantar plane, the prosthesis is aligned taking as reference the axis of the second metatarsal bone, with the foot in neutral position (Roukis, 2015). In this regard, there are no specific mechanical-articular considerations as for the lateral and frontal planes. However, it is expected that misalignments of the prosthesis in the dorsoplantar plane may involve the presence of antero-medial pain in the ankle in the long term (at least 1 year after surgery).
At present, no previous studies have verified whether there is a relation between the rotational alignment of the talar component in the dorsoplantar plane and the frequency of antero-medial ankle pain, at least 1 year after surgery. This evaluation can provide useful information for a more advantageous placement of the implant during the intervention.
Aim of the Study:
The aim of the study is to evaluate the relation between the rotational alignment of the talar component (phi angle) and the antero-medial ankle pain, in patients underwent total ankle replacement, at least one year after surgery.
Moreover, the study aims to define a range of the phi angle associated with a lower frequency of the antero-medial pain.
Methods:
A sample of 100 subjects in the follow-up period after total ankle replacement (minimum 12 months after surgery, maximum 36 months) will be enrolled. Age range will be 18 to 60 years. Each subject will be evaluated once, in occasion of the routine follow-up examination. The subjects will be enrolled consecutively and differentiated according to the time passed since the intervention (at least 12 months), with incremental windows of 6 months, up to a maximum of 36 months. This will lead to define 4 time windows (12-18 months, 18-24, 24-30, 30-36). A number of 25 subjects will be enrolled for each time window. Once a time window will be completed, only subjects belonging to the remaining not completed windows will be enrolled.
Outcomes:
The phi angle will be measured according to that described by Manzi et al., 2017. Specifically, the phi angle will be obtained by the orthopaedist on the standard dorsoplantar radiograph of the foot, which is routinely performed for the follow-up examination. The phi angle is the relative angle between the alignment of the talar component of the implant, and the axis passing through the second metatarsal bone, in the dorsoplantar plane. The phi angle is defined as negative when the talar component is aligned in an abducted position to the second metatarsal axis; similarly, the angle is defined as positive when the talar component is aligned in an adducted position.
The rate of postoperative pain will be assessed during the follow-up examination by a recently distributed pain monitoring web-based app: 'NavigatePain' (NavigatePain, Aglance Solutions, Denmark). The app is used in a simple and intuitive manner by exploiting tablet device (Boudreau, 2016; Matthews, 2018). It is used only for data collection, without therapeutic or diagnostic purposes. In few minutes, it allows the patient to draw the pain areas in the frontal and lateral planes, automatically providing an index that quantifies the percentage of anterior and medial areas affected by pain (with respect to the whole body area in the considered plane).
The antero-medial ankle pain will be obtain as the sum of the anterior and medial pain indexes provided by the app.
The strength of the relation between the phi angle and the antero-medial ankle pain will be evaluated according to Pearson correlation coefficient, or Spearman rank correlation in case of not normal distribution. Statistical significance of the coefficients will be tested according to two-tailed t-test or permutation distribution test assessing Pearson and Spearman coefficients, respectively. Linear regression analysis will be performed as well.
Correlation coefficient and linear regression will be evaluated in each time window. The results will be compared among the consecutive windows in order to assess the potential dependence on the follow-up time.
The sample size of 25 subjects per time window has been verified to guarantee identifying as significantly different from zero a correlation value larger than 0.7 (i.e. strong correlation), by t-test at 0.05 level alpha and power 95% (G*Power software, Universitat Dusseldorf, Germany).
The distribution of the pain rate will be evaluated in function of the phi angle. Potential threshold values of phi associated with lower pain rates will be identified, in order to define a range of phi associated with a lower frequency of the antero-medial pain.
- Conditions
- Ankle Osteoarthritis, Prostheses and Implants
- Keywords
- Total Ankle Replacement; Pain Measurement
What is being measured
The primary outcome is the main question the study is designed to answer.
Phi angle
Relative angle (measured in degrees) between the alignment of the talar component of the implant, and the axis passing through the second metatarsal bone, in the dorsoplantar plane.
Measured: Through study completion, an average of 18 months
Antero-medial ankle pain
Sum of the antero and medial pain areas, measured as percentage with respect to the total body area in the considered plane.
Measured: Through study completion, an average of 18 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted11 Dec 2018
- Study start4 Dec 2018
- Primary completion30 Jun 2020 (estimated)
- Study completion30 Jun 2020 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (5)Papers the sponsor has linked to this study.
- Other trials for Ankle OsteoarthritisStudies of the same condition, open and under way.
- More trials run by I.R.C.C.S Ospedale Galeazzi-Sant'AmbrogioThe sponsor's other registered studies.
- 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 only
- Time perspective
- Cross-sectional
- Enrolment
- 100 participants (estimated)
Sponsor and investigators
- Lead sponsor
- I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Federico Usuelli, MD, Principal investigator, IRCCS Istituto Ortopedico Galeazzi
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03772236
- Sponsor's protocol ID
- ARP2
- Status last verified
- Dec 2018
- First submitted
- 10 Dec 2018
- Last updated
- 14 Dec 2018
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Boudreau SA, Badsberg S, Christensen SW, Egsgaard LL. Digital Pain Drawings: Assessing Touch-Screen Technology and 3D Body Schemas. Clin J Pain. 2016 Feb;32(2):139-45. doi: 10.1097/AJP.0000000000000230.
PubMed 25756558Manzi L, Villafane JH, Indino C, Tamini J, Berjano P, Usuelli FG. Reliability of the Phi angle to assess rotational alignment of the talar component in total ankle replacement. Foot Ankle Surg. 2019 Apr;25(2):169-173. doi: 10.1016/j.fas.2017.10.009. Epub 2017 Nov 8.
PubMed 29409284Matthews M, Rathleff MS, Vicenzino B, Boudreau SA. Capturing patient-reported area of knee pain: a concurrent validity study using digital technology in patients with patellofemoral pain. PeerJ. 2018 Mar 8;6:e4406. doi: 10.7717/peerj.4406. eCollection 2018.
PubMed 29568700Roukis TS. The Salto Talaris XT Revision Ankle Prosthesis. Clin Podiatr Med Surg. 2015 Oct;32(4):551-67. doi: 10.1016/j.cpm.2015.06.019. Epub 2015 Jul 31.
PubMed 26407741Saltzman CL, Tochigi Y, Rudert MJ, McIff TE, Brown TD. The effect of agility ankle prosthesis misalignment on the peri-ankle ligaments. Clin Orthop Relat Res. 2004 Jul;(424):137-42. doi: 10.1097/01.blo.0000132463.80467.65.
PubMed 15241155
Study at a glance
From the registry record, last updated by the sponsor on 14 Dec 2018. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Evaluation of the Relation Between the Rotation Angle of the Talar Component and the Antero-medial Pain in Patients Underwent Total Ankle Replacement, at Least One Year After Surgery
- ClinicalTrials.gov ID
- NCT03772236
- Acronym / sponsor ID
- ARP2
- Conditions
- Ankle Osteoarthritis, Prostheses and Implants
- Keywords
- Total Ankle Replacement; Pain Measurement
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 100 participants (estimated)
- Lead sponsor
- I.R.C.C.S Ospedale Galeazzi-Sant'AmbrogioUniversity, hospital or other
- Study start
- 4 Dec 2018 (actual)
- Primary completion
- 30 Jun 2020 (estimated)
- Study completion
- 30 Jun 2020 (estimated)
- First posted
- 11 Dec 2018 (actual)
- 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.
The study evaluates the relation between the rotational alignment of the talar component (phi angle) and the antero-medial ankle pain in patients underwent total ankle replacement, at least one year after surgery.
Moreover, the study aims to define a range of the phi angle associated with a lower frequency of antero-medial pain.
Detailed description
Background:
In case of total ankle prosthesis surgery, the correct positioning of the talar component is one of the most challenging tasks. When performing total ankle replacement, the primary goal for long-term implant survival is to restore a physiological alignment of the prosthesis in the lateral and frontal planes. In fact, an incorrect alignment can alter joint mechanics and joint reactive forces that can lead to implant failure (Saltzman, 2004).
Regarding the rotation in the dorsoplantar plane, the prosthesis is aligned taking as reference the axis of the second metatarsal bone, with the foot in neutral position (Roukis, 2015). In this regard, there are no specific mechanical-articular considerations as for the lateral and frontal planes. However, it is expected that misalignments of the prosthesis in the dorsoplantar plane may involve the presence of antero-medial pain in the ankle in the long term (at least 1 year after surgery).
At present, no previous studies have verified whether there is a relation between the rotational alignment of the talar component in the dorsoplantar plane and the frequency of antero-medial ankle pain, at least 1 year after surgery. This evaluation can provide useful information for a more advantageous placement of the implant during the intervention.
Aim of the Study:
The aim of the study is to evaluate the relation between the rotational alignment of the talar component (phi angle) and the antero-medial ankle pain, in patients underwent total ankle replacement, at least one year after surgery.
Moreover, the study aims to define a range of the phi angle associated with a lower frequency of the antero-medial pain.
Methods:
A sample of 100 subjects in the follow-up period after total ankle replacement (minimum 12 months after surgery, maximum 36 months) will be enrolled. Age range will be 18 to 60 years. Each subject will be evaluated once, in occasion of the routine follow-up examination. The subjects will be enrolled consecutively and differentiated according to the time passed since the intervention (at least 12 months), with incremental windows of 6 months, up to a maximum of 36 months. This will lead to define 4 time windows (12-18 months, 18-24, 24-30, 30-36). A number of 25 subjects will be enrolled for each time window. Once a time window will be completed, only subjects belonging to the remaining not completed windows will be enrolled.
Outcomes:
The phi angle will be measured according to that described by Manzi et al., 2017. Specifically, the phi angle will be obtained by the orthopaedist on the standard dorsoplantar radiograph of the foot, which is routinely performed for the follow-up examination. The phi angle is the relative angle between the alignment of the talar component of the implant, and the axis passing through the second metatarsal bone, in the dorsoplantar plane. The phi angle is defined as negative when the talar component is aligned in an abducted position to the second metatarsal axis; similarly, the angle is defined as positive when the talar component is aligned in an adducted position.
The rate of postoperative pain will be assessed during the follow-up examination by a recently distributed pain monitoring web-based app: 'NavigatePain' (NavigatePain, Aglance Solutions, Denmark). The app is used in a simple and intuitive manner by exploiting tablet device (Boudreau, 2016; Matthews, 2018). It is used only for data collection, without therapeutic or diagnostic purposes. In few minutes, it allows the patient to draw the pain areas in the frontal and lateral planes, automatically providing an index that quantifies the percentage of anterior and medial areas affected by pain (with respect to the whole body area in the considered plane).
The antero-medial ankle pain will be obtain as the sum of the anterior and medial pain indexes provided by the app.
The strength of the relation between the phi angle and the antero-medial ankle pain will be evaluated according to Pearson correlation coefficient, or Spearman rank correlation in case of not normal distribution. Statistical significance of the coefficients will be tested according to two-tailed t-test or permutation distribution test assessing Pearson and Spearman coefficients, respectively. Linear regression analysis will be performed as well.
Correlation coefficient and linear regression will be evaluated in each time window. The results will be compared among the consecutive windows in order to assess the potential dependence on the follow-up time.
The sample size of 25 subjects per time window has been verified to guarantee identifying as significantly different from zero a correlation value larger than 0.7 (i.e. strong correlation), by t-test at 0.05 level alpha and power 95% (G*Power software, Universitat Dusseldorf, Germany).
The distribution of the pain rate will be evaluated in function of the phi angle. Potential threshold values of phi associated with lower pain rates will be identified, in order to define a range of phi associated with a lower frequency of the antero-medial pain.
Study design
- Observational model
- Case only
- Time perspective
- Cross-sectional
Who may qualify
- Ages
- 18 to 60 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult
- Study population
- Patients undergoing follow-up examination at a third-level hospital after total ankle replacement
Key inclusion criteria (1 listed)
- previous intervention of first implant of total ankle replacement, with at least 12 months of follow up and maximum 36 months
Key exclusion criteria (3 listed)
- more than 36 months from the surgery of first implant of total ankle replacement
- previous revision surgery of ankle prosthesis
- previous intervention of ankle disarthrodesis and ankle prosthesis implant
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Phi angle
Time frame: Through study completion, an average of 18 months
Relative angle (measured in degrees) between the alignment of the talar component of the implant, and the axis passing through the second metatarsal bone, in the dorsoplantar plane.
Antero-medial ankle pain
Time frame: Through study completion, an average of 18 months
Sum of the antero and medial pain areas, measured as percentage with respect to the total body area in the considered plane.
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 14 Dec 2018.
- Background: PubMed 25756558Boudreau SA, Badsberg S, Christensen SW, Egsgaard LL. Digital Pain Drawings: Assessing Touch-Screen Technology and 3D Body Schemas. Clin J Pain. 2016 Feb;32(2):139-45. doi: 10.1097/AJP.0000000000000230.
- Background: PubMed 29409284Manzi L, Villafane JH, Indino C, Tamini J, Berjano P, Usuelli FG. Reliability of the Phi angle to assess rotational alignment of the talar component in total ankle replacement. Foot Ankle Surg. 2019 Apr;25(2):169-173. doi: 10.1016/j.fas.2017.10.009. Epub 2017 Nov 8.
- Background: PubMed 29568700Matthews M, Rathleff MS, Vicenzino B, Boudreau SA. Capturing patient-reported area of knee pain: a concurrent validity study using digital technology in patients with patellofemoral pain. PeerJ. 2018 Mar 8;6:e4406. doi: 10.7717/peerj.4406. eCollection 2018.
- Background: PubMed 26407741Roukis TS. The Salto Talaris XT Revision Ankle Prosthesis. Clin Podiatr Med Surg. 2015 Oct;32(4):551-67. doi: 10.1016/j.cpm.2015.06.019. Epub 2015 Jul 31.
- Background: PubMed 15241155Saltzman CL, Tochigi Y, Rudert MJ, McIff TE, Brown TD. The effect of agility ankle prosthesis misalignment on the peri-ankle ligaments. Clin Orthop Relat Res. 2004 Jul;(424):137-42. doi: 10.1097/01.blo.0000132463.80467.65.
- Individual participant dataSharing planned: No
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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.
Federico Usuelli, MD principal investigator
IRCCS Istituto Ortopedico Galeazzi
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 Ankle Osteoarthritis and Prostheses and Implants, run by I.R.C.C.S Ospedale Galeazzi-Sant'Ambrogio at 1 site in Italy.
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 3 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: status not confirmed, as of the sponsor's last update on 14 Dec 2018. 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 Italy. 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?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Tito Bassani, PhD (+390266214939, tito.bassani@grupposandonato.it), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Phi angle (time frame: Through study completion, an average of 18 months). 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?
On the ClinicalTrials.gov record for NCT03772236, which also lists 5 linked publications.
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 14 Dec 2018.