A clinical trial about the after-treatment of anterior cruciate ligament reconstruction using hamstring tendons with and without wearing an orthosis - a prospective randomized study

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00011774

Enrollment

136

Registered

2017-03-02

Start date

2016-07-01

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

M23.61 S83.53

Interventions

Group 1: Arm 1 - After-Treatment after ACL Ruptur without any orthesis Group 2: Arm 2 - Controll - After ACLR the participants are wearing a knee-stabilizing hard-brace for 6 weeks.

Eligibility

Sex/Gender

All

Age

18 Years to 60 Years

Inclusion criteria

Inclusion criteria: isolated first rupture of anterior cruciate Ligament, normal bodyweight (BMI <35), Age between 18 and 60

Exclusion criteria

Exclusion criteria: multiple Ligament injury, previous Ligament Operation, gonarthrosis, cartilage replacement, meniscus tear

Design outcomes

Primary

Measure	Time frame
Equivalenz in subjective IKDC 2000 Knee Score 12 month post OP	—

Secondary

Measure	Time frame
Time of Acquisition disability, Quality of life (SF36), Tegner and Lysholm Score, 12 month post OP	—

Countries

Germany

Contacts

Public ContactTobias Ohmann

BG Klinikum Duisburg

tobias.ohmann@bg-klinikum-duisburg.de0203 7688 3129

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026