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knee joint design, vitamin D and steroid abuse as risk factor for bony soft tissue Injury

Anatomical factors, vitamin D and anabolic steroid abuse as risk factor for Anterior Cruciate Ligament Injury

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2017/09/009616
Enrollment
100
Registered
2017-09-04
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Patients with Anterior cruciate ligament tear

Interventions

Control Intervention1: Anatomical risk factors (Intercondylar notch geometry, Geometry of Tibial Plateau, ACL Dimensions, Generalized Laxity, Knee Joint Laxity), anabolic steroid abuse , Vitamin D lev

Sponsors

Department Of Science and Technology Chandigarh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: For injured group- Inclusion criteria are i)-patients within 18 to 40 years of age; ii)-patients whose ACL injury is confirmed by some investigation or intervention at some point of time. For non-injured group- Inclusion criteria are i)-persons within 18 to 40 years of age. ii)- persons with no history of ACL injury.

Exclusion criteria

Exclusion criteria: For injured group- Exclusion criteria are i) patients with direct contact injuries or high-energy violence injuries, such as car accident and falling accidents. ii) patients with bilateral knee joint injuries. iii) patients with uneven density on the intercondylar notch and articular surfaces, with condyle osteophyte formation on median and lateral femur as well as on tibial intercondylar eminence or with obvious degeneration of the knee joint. iv) patients with a past history of knee joint tuberculosis, suppurative arthritis, rheumatism or rheumatoid arthritis, osteoarthritis and other bony knee joint diseases. v) Patients with history of trauma to lower limb, with congenital deformity/obvious skeletal deformity of lower limb. For non-injured group- Exclusion criteria are- i)-persons with uneven density on the intercondylar notch and articular surfaces, with condyle osteophyte formation on median and lateral femur as well as on tibialintercondylareminence or with obvious degeneration of the knee joint. ii) persons with a past history of knee joint tuberculosis, suppurative arthritis, rheumatism or rheumatoid arthritis, osteoarthritis and other bony knee joint diseases. iii) Patients with history of trauma to lower limb, with congenital deformity/obvious skeletal deformity of lower limb.

Design outcomes

Primary

MeasureTime frame
Comparison of anatomical variables of knee geometry between injured group and non-injured group. b)-Comparison of knee joint laxity and generalized joint and ligamentous laxity between injured group and non-injured group. c)-Comparison of Vitamin D levels in injured group and non-injured group. d)-Comparison of anabolic steroid abuse in injured group and non-injured group. Timepoint: 1 year and 6 months

Secondary

MeasureTime frame
NATimepoint: NA

Countries

India

Contacts

Public ContactDr Sanjay

Government Medical College and Hospital

sanjayjhatiwal0119@gmail.com9646174269

Outcome results

None listed

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