- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05475626
Treatment Of Symptomatic Pes Planus By Sinus Tarsi Screw Versus Conical Subtalar Screw Arthroereisis
July 23, 2022 updated by: Mahmoud Ali Hassan Abdelhamid
Treatment Of Symptomatic Pes Planus By Sinus Tarsi Screw Versus Conical Subtalar Screw Arthroereisis- A Randomised Controlled Study
compare the outcome of surgical treatment planus by sinus tarsi screw versus conical subtalar screw arthroereisis
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
Pes planus occurs as a result of loss of the medial longitudinal arch, abduction of the forefoot and excessive subtalar eversion.
It can broadly be categorized as rigid or flexible.(1)
Flexible pes planus has no single identifiable cause and is often asymptomatic.(1-3)
Patients with pesplanus had a very tight achilles tendon due to compensatory motion.(4)
It can become painful and may require orthopaedic or pediatric intervention.
Common treatment modalities include rest, physiotherapy, orthotics and anti-inflammatories.(1,3,5-6) Surgery is uncommon unless pain persists in spite of nonsurgical management.(5-6)
Surgical options include soft tissue procedures, realignment osteotomies and non-fusion motion-limiting techniques.(1,2,6-9)
Fusion of selected joints in the foot is not recommended in paediatric patients unless associated with a neuromuscular pathology.(1,5)
Subtalar arthroereisis is a recognized non-fusion surgical treatment for symptomatic paediatric flexible pes planus.
Arthroereisis (also arthroreisis, arthrorhisis or arthrorisis) derives from Greek, translated as to prop up or support a joint.(10)
When Flexible pes planus becomes symptomatic, affecting gait and limiting quality of life, and conservative treatment such as weight reduction, physiotherapy or insoles fail, operative treatment can be considered .(7)
There are two techniques for subtalar arthroereisis: (11) Insertion of an implant directly into the sinus tarsi to prevent it collapsing down.
(10) Screw insertion into the lateral side of either the talus or calcaneus(12).
Calcaneo-stop method with cancellous screw insertion into sinus tarsi for subtalar arthroresis is a valid procedure for this multiplanar deformity.
Maintaince of correction of the deformity is achieved via a prioprioceptive mechanism.
(13) The current research is the first one to compare the clinical , radiological,and patient satisfaction outcome of planovalgus cases treated with two different types of subtalar arthroereisis implants .
The purpose of this prospective study is to show the best technique to achieve patient satisfaction.
Study Type
Observational
Enrollment (Anticipated)
50
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: mahmoud ali, master
- Phone Number: 01093192729
- Email: mahmoudali203@yahoo.com
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
7 years to 15 years (Child)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Patients above the ages of 7years
• All patients with symptomatic pes planus
Description
Inclusion Criteria:
- Patients are eligible for participation in the study if
- Patients above the ages of 7years
- All patients with symptomatic pes planus
- flexible flat feet
- Not respond to conservative therapies.
Exclusion Criteria:
Patients are excluded for participation in the study if
- Patients were age < 7 years
- Asymptomatic patient
- Rigid flat feet
- Unfit for surgery
- Children with neuromuscular diseases, post traumatic or congenital pes planovalgus will be excluded from the study
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Other
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Treatment Of Symptomatic Pes Planus By Sinus Tarsi Screw
Treatment Of Symptomatic Pes Planus
|
Surgical options include soft tissue procedures, realignment osteotomies and non-fusion motion-limiting techniques.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
to identify and evaluate the comparison between two technical procedure of surgical treatment of symptomatic pes planus by sinus tarsi screw versus conical subtalar screw arthroerasis using American Orthopaedic Foot and Ankle Society scores (AOFAS)
Time Frame: 2 years
|
American Orthopedic Foot & Ankle Society (AOFAS) ankle-hind foot score was assessed.
The total AOFAS score 100 points divided to 40 points for assessment of pain, 50 points for the functional assessment " activity limitations, maximum walking distance, gait abnormality…etc" and 10 points for assessment of the alignment.
|
2 years
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
): to detect the radiographic measurments change between the surgical treatment of symptomatic pes planus by sinus tarsi screw versus conical subtalar arthroerasis
Time Frame: 1 year
|
RadiologicalEvaluation(AP&lateral)withangleevaluation:Radiographswillbe takenpreoperatively,directlypostoperatively,andatmidtermfollow-upina weight-bearingstandingposition.Thecalcanealpitch(CP)andMeary'sangle (MA;alsoreferredtoaslateraltalo-firstmetatarsalangle)willbeusedto determinefootanatomy
|
1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Carr JB II, Yang S, Lather LA. Pediatric pes planus: a state-of-the-art review.Pediatrics 2016;137:e20151230. 2. Dare DM, Dodwell ER. Pediatric flatfoot: cause, epidemiology, assessment, and treatment. Curr Opin Pediatr 2014;26:93-100. 3. Mosca VS. Flexible flatfoot in children and adolescents. J Child Orthop 10;4:107-121. 4. Raj MA, Tafti D, Kiel J. Pes Planus (Flat Feet). StatPearl-NCBI Bookshelf, 2020. Available from: https://www.ncbi.nlm.nih.gov/books/NBK430802/ (Accessed 29 June 2020) 5.Sheikh Taha AM, Feldman DS. Painful flexible flatfoot. Foot Ankle Clin 2015;20:693-704. 6. Bouchard M, Mosca VS. Flatfoot deformity in children and adolescents: surgical indications and management. J Am Acad Orthop Surg 2014;22:623-632. 7. Walters JL, Mendicino SS. Flexible adult flatfoot: soft tissue procedures. Clin Podiatr Med Surg 2014;31:349-355. 8. Peterson KS, Overley BD Jr, Beideman TC. Osteotomies for the flexible adult acquired flatfoot disorder. Clin Podiatr Med Surg 2015;32:389-403. 9. Abubeih ,Hossam MA.,Wael El-Adly ,and Kotb,M.M. Modified calcaneo-stop screw method for treatment of symptomatic pediatric flexible flatfoot deformity . Current Orthopaedic Practice 26.6 (2015);614-618. 10. Medical Dictionary. Arthroereisis. The Free Dictionary. https://medical-dictionary. The free dictionary .com/arthroereisis (date last accessed 5 July 2018). 11. Chambers EF. An operation for the correction of flexible flat feet of adolescents. West J Surg Obstet Gynecol 1946;54:77-86. 12. Shah NS, Needleman RL, Bokhari O, Buzas D. 2013 subtalar arthroereisis survey: the current practice patterns of members of the AOFAS. Foot Ankle Spec 2015;8: 180-185 13. Staheli L. Planovalgus foot deformity.Current status.Journal of the American Podiatric Medical Association 1999;89(2): 94-9. 14. Ritchie GW and Keim HA .A radiographic analysis of major foot deformities.Canad Med Ass J Oct 1963;Vol 91 .
Helpful Links
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Anticipated)
August 30, 2022
Primary Completion (Anticipated)
May 30, 2023
Study Completion (Anticipated)
May 30, 2024
Study Registration Dates
First Submitted
July 20, 2022
First Submitted That Met QC Criteria
July 23, 2022
First Posted (Actual)
July 27, 2022
Study Record Updates
Last Update Posted (Actual)
July 27, 2022
Last Update Submitted That Met QC Criteria
July 23, 2022
Last Verified
July 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Randomized controlled study
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Undecided
IPD Plan Description
Treatment Of Symptomatic Pes Planus By Sinus Tarsi Screw Versus Conical Subtalar Screw Arthroereisis- A Randomised Controlled Study
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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