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Prospective Hamstring Avulsion Registry for Outcome following Surgical and nonoperative treatment

Prospective Hamstring Avulsion Registry for Outcome following Surgical and nonoperative treatment - PHAROS

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON55253
Enrollment
1000
Registered
2021-05-04
Start date
2021-05-06
Completion date
Unknown
Last updated
2024-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

avulsion of the hamstring tendons Full-thickness injury of the hamstring tendons

Interventions

None listed

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - Aged >=18years - MRI- and/or ultrasound-confirmed proximal or distal full-thickness free tendon hamstring injury of the biceps femoris, semitendinosus muscle and/or semimembranosus muscle.

Exclusion criteria

Exclusion criteria: - Not able or unwilling to give informed consent - Concurrent disease/disorder that renders the patient unable to follow the rehabilitation program

Design outcomes

Primary

MeasureTime frame
- Perth Hamstring Assessment Tool score (PHAT, 0-100)

Secondary

MeasureTime frame
- Rate of return to play (in %) - Time to return to play (days) - Patient-rated recovery and satisfaction (self-reported) - Quality of life score (EQ-5D-3L, 0.0-1.0) - Hamstring strength (isometric, in N) - Imaging (MRI/ultrasound) characteristics (including bone-tendon continuity and fatty degeneration according to the Goutallier classification - Description and rate of adverse events (in %)

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)