NCT05476692

Brief Summary

Assess clinical and radiological outcome of the various surgical techniques for treatment of osteochondral lesions of the talus

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
40

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Oct 2022

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

July 18, 2022

Completed
9 days until next milestone

First Posted

Study publicly available on registry

July 27, 2022

Completed
2 months until next milestone

Study Start

First participant enrolled

October 1, 2022

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2023

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2023

Completed
Last Updated

July 27, 2022

Status Verified

July 1, 2022

Enrollment Period

1 year

First QC Date

July 18, 2022

Last Update Submit

July 26, 2022

Conditions

Outcome Measures

Primary Outcomes (1)

  • clinical outcome of the various surgical techniques for treatment of osteochondral lesions of the talus

    clinical outcome of the various surgical techniques for treatment of osteochondral lesions of the talus , Clinical outcome by the AOFAS score ( American Orthopaedic Foot and Ankle Society), the higher score means the better outcome and the lower score means the worse outcome

    1 year

Interventions

Clinical outcome by the Visual analogue scale (VAS) and the American Orthopaedic Foot and Ankle (AOFAS) score.

Eligibility Criteria

Age15 Years - 60 Years
Sexall
Age GroupsChild (0-17), Adult (18-64)
Sampling MethodNon-Probability Sample
Study Population

the study is a descriptive case series study. The sample will be included from the admitted 40 patients during 12 months from the start of the study

You may qualify if:

  • Age from 15 to 60 years old.
  • Traumatic and degenerative etiology.
  • without ankle deformity.
  • No inflammatory arthritis.
  • Absent or corrected ligamentous instability

You may not qualify if:

  • Older than 60 years old and younger than 15 years old.
  • Charcot ankle.
  • Vascular injury.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Related Links

Central Study Contacts

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

July 18, 2022

First Posted

July 27, 2022

Study Start

October 1, 2022

Primary Completion

October 1, 2023

Study Completion

November 1, 2023

Last Updated

July 27, 2022

Record last verified: 2022-07