At a glance
ClinicalIndex Comparison RecordN/ACompleted· 216 enrolled
Drug / intervention
Surgical reattachment of hamstring tendonsprocedure
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
The Proximal Hamstring Avulsion Clinical Trial - Nonoperative Treatment Compared With Suture Anchor Reinsertion of Proximal Hamstrings Avulsions
In Brief
A clinical study evaluating Surgical reattachment of hamstring tendons for Hamstring Tendon Injury. Completed, enrolled 216 participants across 10 sites in 2 countries.
Detailed Summary
The purpose of this study is to provide reliable evidence on how to best treat proximal hamstrings avulsions, and our primary aim is to compare the reported outcome of patients treated non-operatively with patients treated with suture anchor reattachment of the tendons using the Perth Hamstrings Assessment Tool (PHAT) at 24 months.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHamstring Tendon Injury
CountriesNorway, Sweden
Timeline
N/ACompletedFinished
201820192020202120222023202420252026
First PostedOct 2017
Enrollment StartOct 2017
Primary CompletionSep 2022
TodayJul 2026
First PostedOct 17, 2017
Enrollment StartOct 24, 2017
Primary CompletionSep 22, 2022
TodayJul 2, 2026
Enrollment to primary: 4.9 yearsPosted 8.7 years ago
Interventions
Surgical reattachment of hamstring tendonsprocedure
operatively reattachment of the tendons using suture anchor