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The Proximal Hamstring Avulsion Clinical Trial - Operative or Nonoperative Treatment

NCT03311997 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 216

Last updated 2024-04-11

No results posted yet for this study

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.

Conditions

  • Hamstring Tendon Injury

Interventions

PROCEDURE

Surgical reattachment of hamstring tendons

operatively reattachment of the tendons using suture anchor

Sponsors & Collaborators

  • Linkoeping University

    collaborator OTHER_GOV

  • Lund University

    collaborator OTHER

  • Örebro University, Sweden

    collaborator OTHER

  • Umeå University

    collaborator OTHER

  • Karolinska Institutet

    collaborator OTHER

  • University of Oslo

    collaborator OTHER

  • University of Bergen

    collaborator OTHER

  • Uppsala University

    lead OTHER

Principal Investigators

  • Kenneth Jonsson, MD., Ph.D · Uppsala University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
30 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-10-24
Primary Completion
2022-09-22
Completion
2022-09-22

Countries

  • Norway
  • Sweden

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03311997 on ClinicalTrials.gov