AzTrials
AzTrials

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.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
Search all trials

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
  • Irccs Istituto Ortopedico Galeazzi

    Milan, Milano, 20156

    Federico Usuelli, MD, +39‭3357351838‬, fusuelli@gmail.com

    Federico Usuelli, MD

    Recruiting

Other trials in Italy

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.

Keywords
Total Ankle Replacement; Pain Measurement

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. 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

  2. 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.

  1. First posted11 Dec 2018
  2. Study start4 Dec 2018
  3. Primary completion30 Jun 2020 (estimated)
  4. Study completion30 Jun 2020 (estimated)

Resources

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)
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 25756558
  • Manzi 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 29409284
  • Matthews 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 29568700
  • Roukis 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 26407741
  • Saltzman 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

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.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in