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Evaluation of Osteopathic Care After Rupture of the Antero-external Cruciate Ligament of the Knee (DIDT OSTEO)

Evaluation of Osteopathic Care After Rupture of the Antero-external Cruciate Ligament of the Knee

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05875766
Acronym
DIDT OSTEO
Enrollment
94
Registered
2023-05-25
Start date
2023-04-07
Completion date
2024-12-07
Last updated
2023-05-25

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

Conditions

Cruciate Ligament Rupture, Knee Ligament Injury, Osteopathia

Brief summary

The antero-external cruciate ligament (ACL) is the ligament located inside the knee, which allows the rotation of the knee by stabilizing the femur and the tibia. Rupture of the ACL is common during the practice of certain so-called pivot sports, whether contact or not. It is manifested by acute pain or instability of the knee, following a crack during a twist and/or a blockage of the joint. The diagnosis will be confirmed by a clinical examination and X-rays to eliminate any fracture or tearing and by MRI to visualize the ligament rupture and the associated lesions, in particular a lesion of the meniscus. Treatment is required because the ruptured ligament does not heal on its own and the rupture of the ligament may eventually promote the appearance of osteoarthritis. Two types of treatment can be considered, rehabilitation or surgery, depending on the patient's age and motivation to resume sports. There are several surgical techniques, the most common is to reconstruct the ruptured ligament by arthroscopy using a graft taken from the tendons of the Internal Rectus and Demi muscles tendinous (DIDT). Rehabilitation by physiotherapy is often started preoperatively and immediately after the operation, as soon as you wake up, to find a functional and painless knee. Functional recovery often depends on patient motivation. The main objective is to show that osteopathic care in addition to physiotherapy rehabilitation improves knee functionality in patients 6 months after reconstruction of the ACL by DIDT.

Interventions

4 sessions of osteopathy after DIDT surgery

OTHERPhysiotherapy

Physiotherapy after DIDT surgery (reference treatment)

Sponsors

Ramsay Générale de Santé
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 35 Years
Healthy volunteers
No

Inclusion criteria

* Patient, male or female, aged 18 to 35 inclusive * Patient with a BMI between 18.5 and 30 kg/m² (limits included). * Patient presenting with a total rupture of the unilateral anterior cruciate ligament (ACL). * Candidate patient for reconstruction of the ACL with the DIDT method. * Affiliated patient or beneficiary of a social security scheme. * Patient having been informed and having given their free consent, enlightened and written.

Exclusion criteria

* Patient with damage to another structure of the knee, other than meniscal lesions. * Patient with a contraindication to osteopathic intervention. * Patient for whom a method other than DIDT has been proposed. * Patient with iterative rupture of the ACL. * Patient having undergone ligamentoplasty of the contralateral knee * Patient participating in another research. * Patient in period of exclusion from another research still in progress at the time of inclusion. * Protected patient: adult under guardianship, curatorship or other legal protection, deprived of liberty by judicial or administrative decision. * Pregnant, breastfeeding or parturient women. * Patient hospitalized without consent.

Design outcomes

Primary

MeasureTime frameDescription
assess the functionality of the knee6 monthsUsing International Knee Documentation Committee Subjective Knee Form (IKDC) measured 6 months postoperative and referring to the last weeks.

Countries

France

Contacts

Primary ContactJean-François Oudet
jf.oudet@ecten.eu0683346567
Backup ContactMarie Hélène Barba
mh.barba@ecten.eu

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026