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A study to assess success after knee surgery

A Randomized, Multi Center, Parallel, Open Label Study Assessing Clinical and Functional Outcomes After Anterior Cruciate Ligament (ACL) Reconstruction Procedure Using Suspensory Tibial Fixation with Open and Closed Peek Button

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/04/051751
Enrollment
80
Registered
2023-04-19
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Health Condition 1: M999- Biomechanical lesion, unspecified

Interventions

Intervention1: Peek button-closed (T-Buttonâ?¢ A PEEK Adjustable Loop Button): Peek button-closed (T-Buttonâ?¢ A PEEK Adjustable Loop Button) is used for tibial fixation of the graft and will stay per

Sponsors

Healthium Medtech Limited
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Male/ female participants between >=18 years and 2. Participants with traumatic ACL tears with or without associated meniscus injuries requiring primary ACL reconstruction surgery 3. Participants/ Legally Acceptable Representative who are willing to provide written Informed Consent and comply with study procedures

Exclusion criteria

Exclusion criteria: 1. Participants with lateral/medial collateral ligament injury or posterior cruciate ligament injury 2. Participants with BMI >=35 kg/m2 3. Participants who had undergone previous surgery in the same or contralateral knee 4. Participants with HbA1c Ë? 9% (Clinical laboratory reports up to 3 months will be considered valid otherwise participants will undergo blood investigation for HbA1C) 5. Participants who are smokers (smoking Ë?20 cigarettes/day) 6. Participants with sensitivity to PEEK material 7. Participants with a history of deep vein thrombosis (DVT) 8. Participants with arthritis of same or contralateral knee 9. Participants with any condition which makes the subject unsuitable for study participation which as per the investigator would jeopardize the outcome of the trial or participant who, in the judgment of the investigator, will be unlikely to comply with the requirements of this clinical investigation plan 10. Pregnant and lactating female at the time of screening

Design outcomes

Primary

MeasureTime frame
1. To assess functional outcomes of Knee in each cohort of Peek button-open and Peek button-closed.Timepoint: Screening, month 3, month 6, month 12, month 18 and month 24

Secondary

MeasureTime frame
1. To assess the clinical symptoms and activity level in each cohort of Peek button-open and Peek button-closed from baseline (pre-surgery). 2. To assess the failure rate of ACL reconstruction in each cohort of Peek button-open and Peek button-closed. 3. To assess change in quality of life in patients of each cohort of Peek button-open and Peek button-closed. 4. To assess recovery period in patients of each cohort of Peek button-open and Peek button-closed. 5. To assess the duration of surgery. 6. To assess clinical condition of the knee. 7. To assess the overall intraoperative handling of Peek button-open and Peek button-closed. 8. To assess the incidence of residual risks and safety of peek button open and Peek button closed. 9. To assess the condition of the graft and implants. 10. To compare the results of all primary and secondary objectives between the two cohorts, Peek button-open Vs Peek button-closed.Timepoint: Screening, Day of surgery, Discharge visit, Day 15, month 3, month 6, month 12, month 18 and month 24

Countries

India

Contacts

Public ContactDr Ashok Kumar Moharana

Healthium Medtech Limited

ashok.m@healthiummedtech.com9717887751

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026