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Comparing Anterior cruciate ligament reconstruction surgery outcomes with and without the use of antibiotic solution during graft preparation.

Assessing the outcomes of anterior cruciate ligament reconstruction with or without the use of antibiotic solution in graft preparation: A Randomised control trial - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/11/077019
Enrollment
76
Registered
2024-11-19
Start date
Unknown
Completion date
Unknown
Last updated
2024-12-09

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

Conditions

Health Condition 1: M968- Other intraoperative and postprocedural complications and disorders of musculoskeletal system, not elsewhere classified

Interventions

Intervention1: Vancomycin Antibiotic solution during ACL graft preparation.: Graft is placed in vancomycin solution ( 500 mg of vancomycin powder in 100 mL normal saline) for 10mins to 15 mins during

Sponsors

Rajendra Institute of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: a) Individuals diagnosed with a complete rupture of the ACL who are indicated for surgical reconstruction b) patients willing to provide informed consent to participate in the study c) patients with no history of no prior ACL reconstruction surgery d) patients without significant comorbidities or medical conditions

Exclusion criteria

Exclusion criteria: a) patients with concurrent injuries involving multiple major ligaments of the knee b) patients younger than 18 years or older than 65 years c) patients with previous history of ACL reconstruction of the same knee d) patients with active systemic or local infection

Design outcomes

Primary

MeasureTime frame
To compare the infection rates in patients undergoing ACL reconstruction surgeryTimepoint: Postoperative day(POD)- 2,6,10

Secondary

MeasureTime frame
a) To evaluate the incidence of graft failure(graft rupture or re-tear) between the two study groups b) to explore whether patients characteristics such as age, sex, BMI and previous medical history influence the clinical outcomes and infection rates in both study groupsTimepoint: 1 month and 3 months after surgery

Countries

India

Contacts

Public ContactGovind Kumar Gupta

Rajendra Institute of Medical Sciences , Ranchi

gkgupta1975@yahoo.co.in7979014287

Outcome results

None listed

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