Ligament Plastic Surgery Clinical Trial
— LIGANALYSOfficial title:
Analysis of the Ligamentization Process in the Anatomical Ligamentoplasty of the Lateral Ankle Plane to the Hamstrings
| Verified date | April 2022 |
| Source | Assistance Publique - Hôpitaux de Paris |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Observational |
This is a prospective bi-centric study, which evaluate the evolution of RMI signal of transplant till 12 months after ligament plasty surgery. As the primary objective, the study aims to define the post-operative timeframe needed to obtain an optimal quality of repair, especially in their restarting of sportive activities, by analysis of RMI signal and biomechanic features modifications. As secondary objectives, the study aims to: - study the correlation between the RMI signal of plasty and the Young's modulus; - study the evolution of RMI of plasty at M3, M6 and M12; - study the evolution of Young's modulus at M3, M6 and M12; - evaluate the reproductibility between 2 lector of RMI measurements; - evaluate the reproductibility between 2 lector of elastography measurements of LTFA; - evaluate the optimal delay of return to sport after ligament plasty surgery of ankle; - develope a score of type SNQ for ankle ligament plasty surgery; - evolution of AOFAS and EVA scores.
| Status | Completed |
| Enrollment | 50 |
| Est. completion date | March 30, 2022 |
| Est. primary completion date | March 30, 2022 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years and older |
| Eligibility | Inclusion Criteria: - Patient treated priorly by ligament plastic surgery of lateral ankle plane under arthroscopy; - Affiliated to or covered by the French social security - welfare system in France; - Have provided written informed consent for the study; - Be >/= 18 years of age on day of signing informed consent. Exclusion Criteria: - Patients who undergo iterative surgery or have history of contralateral surgery; - Patient under guardianship or curatorship; - Unable to understand the proposed study or provide written informed consent for the study; - Foreign patients under AME schema, a medical help from the state in France; - Pregnant or breastfeeding woman; - Patient refusal. |
| Country | Name | City | State |
|---|---|---|---|
| France | Orthopaedic Surgery Department, Ambroise Paré hospital, APHP | Boulogne-Billancourt |
| Lead Sponsor | Collaborator |
|---|---|
| Assistance Publique - Hôpitaux de Paris |
France,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Classification of RMI signal | The classification of RMI signal will be defined as:
frank hyposignal: stage 1; intermediary signal (close to muscles of T2): stage 2; moderate hypersignal (close to cartilage of T2): stage 3; intensive hypersignal (close tointra-articular liquid of T2): stage 4. |
At 3 months | |
| Primary | Classification of RMI signal | The classification of RMI signal will be defined as:
frank hyposignal: stage 1; intermediary signal (close to muscles of T2): stage 2; moderate hypersignal (close to cartilage of T2): stage 3; intensive hypersignal (close tointra-articular liquid of T2): stage 4. |
At 6 months | |
| Primary | Classification of RMI signal | The classification of RMI signal will be defined as:
frank hyposignal: stage 1; intermediary signal (close to muscles of T2): stage 2; moderate hypersignal (close to cartilage of T2): stage 3; intensive hypersignal (close tointra-articular liquid of T2): stage 4. |
At 12 months | |
| Secondary | Anterior talofibular ligament measurement | anterior talofibular ligament measurement will be performed by RMI | At 3, 6 and 12 months | |
| Secondary | Calcaneofibular ligament measurement | calcaneofibular ligament measurement will be performed by RMI | At 3, 6 and 12 months | |
| Secondary | Elastography | Elastography measurements: Young's Modulu | At 3, 6 and 12 months | |
| Secondary | Pain evaluation | By the American Orthopedic Foot and Ankle Score (AOFAS) to evaluate the pain. | At baseline and 3, 6 and 12 months | |
| Secondary | Pain evaluation | By the visual analog scale (VAS) to evaluate the pain. | At baseline and 3, 6 and 12 months |