- ICH GCP
- Registro de ensaios clínicos dos EUA
- Ensaio Clínico NCT07569796
Effectiveness of Stimulation on the Sciatic Nerve in ACLR
"Effectiveness of Percutaneous Electrical Nerve Stimulation on the Sciatic Nerve in Patients Undergoing Surgical Reconstruction of the Anterior Cruciate Ligament. A Randomized Clinical Trial".
Visão geral do estudo
Status
Intervenção / Tratamento
Descrição detalhada
Tipo de estudo
Inscrição (Estimado)
Estágio
- Não aplicável
Contactos e Locais
Locais de estudo
-
-
Madrid
-
Madrid, Madrid, Espanha, 28049
- Recrutamento
- Clinica CEMTRO, Montecarmelo, Madrid
-
Contato:
- Adrián Cases Sebastià, Physiotherapist
- Número de telefone: +34 609906468
- E-mail: adriancasese@gmail.com
-
Contato:
- Javier Reina Abellán, PhD
- Número de telefone: +34 656887703
- E-mail: jreina@ucam.edu
-
Investigador principal:
- Adrián Cases Sebastià, Physiotherapist
-
Subinvestigador:
- Luis Blanco López, Physiotherapist
-
Subinvestigador:
- Javier Reina Abellán, PhD
-
Subinvestigador:
- Pedro Guillén García, PhD
-
Subinvestigador:
- Iván Nacher Moltó, PhD
-
-
Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
- Adulto
Aceita Voluntários Saudáveis
Descrição
Inclusion Criteria:
- Use of the Semitendinous and Gracilis tendons for ACL Reconstruction
- Joint Range of Motion greater than or equal to 90
- Primary ACL injury in the leg to be treated
Exclusion Criteria:
- Chronic or rheumatic joint disease
- Central nervous system disorder
- Heart disease (pacemaker)
- Neoplasms
- Epilepsy
- Coagulopathies (use of anticoagulants)
- History of spinal surgery or lumbar disease
- History of neurological disorders
- Prosthesis or osteosynthesis in the operated leg
- Structural discrepancy in lower-limb length
- Belonephobia (overwhelming fear of needles)
- Neuropathic pain or bilateral symptoms
- Use of analgesics
- Quadriceps tendon graft harvest
- Body mass index <20 or >30 kg/m²
- Acute muscle injuries
- Knee joint instability
- Acute joint inflammation
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Tratamento
- Alocação: Randomizado
- Modelo Intervencional: Atribuição Paralela
- Mascaramento: Dobro
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
|
Experimental: Grupo experimental
|
Percutaneous Electrical Nerve Stimulation on the Sciatic Nerve
|
|
Sem intervenção: Grupo de controle
|
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Maximal Isometric Strength of the Hamstring Musculature
Prazo: 5 weeks after surgery
|
Maximal Isometric Strength of the Hamstring Musculature This was recorded with the patient in a prone position, with the knee flexed at 90 degrees and the ankle in plantar flexion. The patient was instructed to perform an isometric knee flexion against a Lafayette hand-held dynamometer, positioned at the level of the Achilles tendon. Three repetitions were recorded and measured in Newtons, with a 60-second rest interval between repetitions. |
5 weeks after surgery
|
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Surface Electromyography of the Hamstring Musculature
Prazo: 5 weeks after surgery
|
This variable was assessed in three different positions. The first position involved the patient lying prone with the knee flexed at 90 degrees and the ankle in plantar flexion. In the second position, the patient was seated at the edge of the examination table with the trunk upright, the hip flexed at 90 degrees, and the knee flexed at 90 degrees, with the ankle in plantar flexion. In the third position, the patient stood in front of the examination table with the injured leg supported on it. The leg was positioned with 90 degrees of hip flexion, 30 degrees of knee flexion, and the ankle in dorsiflexion. The percentage of activation of the biceps femoris and semitendinosus muscles was recorded, as well as the mean activation ratio of these muscles and the peak activation of both. The latter two variables were measured in microvolts. Three repetitions of 5 seconds of activation were performed, with a 60-second rest interval between each repetition. |
5 weeks after surgery
|
|
Postsurgery Pain
Prazo: 5 weeks after surgery
|
NRS scale: 0 = no pain and 10 = the worst pain
|
5 weeks after surgery
|
|
Thigh Circumference Measurement
Prazo: 5 weeks after surgery
|
Thigh circumference was measured using a measuring tape, a validated tool with high inter- and intra-rater reliability in patients with anterior cruciate ligament (ACL) reconstruction. The patient was positioned in a seated posture with the legs hanging off the examination table. The evaluator stood on the ipsilateral side of the operated limb to ensure unobstructed access. The operated knee was maintained in maximal extension, and the patient was instructed to remain relaxed and avoid any contraction of the thigh musculature that could bias the measurement. The evaluator then used the measuring tape to encircle the thigh at a point 10 cm above the superior pole of the patella and recorded the circumference. |
5 weeks after surgery
|
|
Intra-Articular Effusion
Prazo: 5 weeks after surgery
|
Intra-articular effusion was assessed with the patient in a supine position and the knee in extension. The patient was required to remain relaxed to allow accurate assessment of post-surgical joint effusion using the "Stroke test." During this test, the evaluator performed sweeping strokes with the hands from medial to lateral and vice versa, observing the behavior of the effusion and whether it returned to the medial side. This test is graded on a 0-3 scale: 0 indicates no detectable effusion; 1 indicates a measurable fluid wave with a single maneuver; 2 indicates visible fluid with slight pressure; and 3 indicates a large effusion without the need for pressure. This method is validated by the IKDC 2000 (International Knee Documentation Committee) and is widely used in research studies. |
5 weeks after surgery
|
|
Knee Range of Motion
Prazo: 5 weeks after surgery
|
Active and passive knee range of motion was measured using a universal manual goniometer, a highly validated tool commonly used in clinical physiotherapy practice. The patient was positioned supine for accurate measurement. The greater trochanter was identified, and the patient was asked to actively flex the knee by sliding the heel along the table without using the hands. The evaluator stabilized the operated limb with the caudal hand and placed the axis of the goniometer over the lateral femoral condyle. The proximal arm was aligned with the midline of the thigh toward the greater trochanter, and the distal arm with the midline of the leg toward the lateral malleolus. For knee extension, the patient remained in a supine position with the heel, gastrocnemius, and hamstring musculature supported on the table. The patient was then asked to perform active extension, and the goniometer was positioned using the same anatomical landmarks to determine both passive and active extension. |
5 weeks after surgery
|
Colaboradores e Investigadores
Patrocinador
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Real)
Conclusão Primária (Estimado)
Conclusão do estudo (Estimado)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Outros números de identificação do estudo
- CE102505
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
Informações sobre medicamentos e dispositivos, documentos de estudo
Estuda um medicamento regulamentado pela FDA dos EUA
Estuda um produto de dispositivo regulamentado pela FDA dos EUA
Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .
Ensaios clínicos em Experimental Group
-
Abbott NutritionRescindidoInfecções Respiratórias em CriançasEstados Unidos
-
Izmir Democracy UniversityRecrutamento
-
Saglik Bilimleri UniversitesiAinda não está recrutandoEfeito da reflexologia nos sintomas da síndrome pré -menstrual
-
University of ManchesterNational Institute for Health Research, United Kingdom; Greater Manchester Mental...ConcluídoDepressão | Transtornos de ansiedade | Transtorno Mental InfantilReino Unido
-
Aarhus University HospitalUniversity of AarhusConcluídoCâncer de Mama Feminino | Medo da recorrência do câncerDinamarca
-
Cukurova UniversityConcluídoGravidez de alto risco | Estado de ansiedade | Qualidade do SonoPeru
-
Tarsus UniversityRecrutamento
-
University of NottinghamRecrutamento
-
Washington University School of MedicineAtivo, não recrutandoGravidez relacionada | Depressão perinatalEstados Unidos
-
Arizona Oncology ServicesDesconhecidoCâncer de Mama Localizado | Câncer de Próstata Localizado | Pacientes recebendo radioterapia de feixe externoEstados Unidos