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Flexor Tendon Rupture clinical trials

View clinical trials related to Flexor Tendon Rupture.

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NCT ID: NCT06420648 Recruiting - Clinical trials for Flexor Tendon Rupture

Controlled Active Motion vs Early Passive Mobilization for Flexor Tendons Repair

Start date: June 4, 2024
Phase: N/A
Study type: Interventional

a randomized controlled trial tends to compare 2 rehabilitation approaches - early passive mobilization (EPM) and controlled active motion (CAM) - that are commonly used in the treatment of post-surgical flexor tendon repair of the hand

NCT ID: NCT06198582 Completed - Clinical trials for Flexor Tendon Rupture

The Effect of Virtual Reality Based Task Specific Exercises in Patients With Hand Flexor Tendon Injury

Start date: June 1, 2021
Phase: N/A
Study type: Interventional

This study,the investigators aimed to investigate the effects of virtual reality-based task-specific exercises applied in addition to conventional rehabilitation program on functional level and disease-related quality of life in patients who underwent surgical repair due to flexor tendon damage due to traumatic hand injury.

NCT ID: NCT06149962 Recruiting - Clinical trials for Flexor Tendon Rupture

Comparison Between Functional Outcomes of Flexor Tendon Repair Under WALANT and Brachial Plexus Block

Start date: July 10, 2023
Phase: N/A
Study type: Interventional

Although outcomes after flexor tendon repair have reportedly improved with modern treatment, complications are common. Early passive and active motion protocols have improved outcomes of flexor tendon repairs. One potential complication of early motion occurs when the forces produced by this motion exceed the strength of the repair, which leads to gap formation and inhibits healing. Wide Awake Local Anesthesia No Tournique (WALANT) is a new anesthesia technique that has gained popularity among plastic surgeons. It was developed by Dr. Lalonde in Canada, and it involves the use of Lidocaine and adrenaline in the surgical site to control bleeding without the need for a tourniquet. Peripheral nerve blocks are overall safe when performed correctly, there are rare but serious risks associated with them. Risks include block failure, bleeding, infection, damage to surrounding structures, permanent nerve injury, and intravascular uptake of local anesthetic resulting in systemic toxicity.

NCT ID: NCT06112145 Completed - Rehabilitation Clinical Trials

Are Rehabilitation Results in Flexor Tendon Zone II Injuries as Bad as Feared?

Start date: November 1, 2023
Phase: N/A
Study type: Interventional

The hand is the basic functional organ of the human body and is responsible for complex tasks such as grasping and catching. It also plays an important role in a person's daily life, self-care activities and business life. When the flexor tendon system, which is necessary for the effective use of the hand, is damaged, it can cause physical, socioeconomic deterioration, mood disorders and permanent disabilities in the individual. Treatment of flexor tendon injuries after appropriate surgical repair ıt includes an intensive rehabilitation program. In this study, it was aimed to investigate the early rehabilitation results of patients who underwent a rehabilitation program after Zone II flexor tendon injury by comparing the improvements in joint range of motion, pain, functionality and quality of life with other zone injuries.

NCT ID: NCT05809102 Completed - Clinical trials for Flexor Tendon Rupture

Repair Of Flexor Tendon In Zone II Using Minimal Incisions

Start date: February 1, 2020
Phase: N/A
Study type: Interventional

Repair of the zone II flexor tendon of the hand using minimal incisions is successful with good results which will improve the outcome of the repair.

NCT ID: NCT05643079 Recruiting - Clinical trials for Flexor Tendon Rupture

Medial Displacement Calcaneal Osteotomy and FDL- Transfer - With a Human, Allogeneic Cortical Bone Screw

Start date: February 10, 2022
Phase:
Study type: Observational

The goal of this observational study is to compare the use of a screw made of human bone (Shark-Screw®, Surgebright-GmbH) with the metal/Bio-Tenodesis screw (Arthrex) in the treatment of the symptomatic flatfoot using the medializing calcaneus osteotomy with flexor digitorum longus transfer (FDL) in adult patients. The advantage of the human bone screw is that after surgery no hardware removal is necessary. The screw is transformed from the body to normal bone. The main questions it aims to answer are: - Can the human bone screw achieve union rates like the metal/Bio-Tenodesis screw? - Is the time to union similar between the different screws? - Is the complication rate similar between the different screws? - Are the activity scores American Orthopaedic Foot and Ankle Society (AOFAS), Foot and Ankle Outcome Score (FAOS) and Foot Function Index (FFI) after surgery similar in the compared patient groups? Participants will have - the surgery - follow-ups at 6 weeks, 6 months, 1 and 2 years. - X-rays are performed at each follow up. - CT-scans are performed after 6 months. - activity scores are collected at the follow up after 6 months, 1 year and 2 years.

NCT ID: NCT05188040 Completed - Clinical trials for Distal Radius Fracture

Effectiveness of Virtual Reality in Hand Therapy

Start date: May 16, 2022
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if the use of Virtual Reality as an intervention for patients following specific hand injuries will positively affect patients with decreased hand function and reduce pain and improve outcomes. Participants will be recruited from 3 different clinics in central Kentucky.

NCT ID: NCT05148585 Recruiting - Clinical trials for Flexor Tendon Rupture

Efficacy Of Activity-Based Intervention On Activity, Participation And Kinesiophobia In Patients With Tendon Injury

Start date: February 24, 2020
Phase: N/A
Study type: Interventional

The aim of our study is to determine the effect of activity-based intervention on the activity, participation levels and kinesiophobia (fear of movement) of the patients by evaluating the person, environment and activity using the Person-Environment-Occupation model (PEO) in the rehabilitation of hand forearm flexor tendon injuries.

NCT ID: NCT05095415 Not yet recruiting - Clinical trials for Distal Radius Fracture

Occupational Therapy Pre-operative Education in the Orthopedic Hand Setting

Start date: October 2021
Phase: N/A
Study type: Interventional

This will be a prospective randomized control trial with a blocking method to determine the effect of an occupational therapy focused pre-operative education on 3 pre-determined diagnosis: Carpometacarpal (CMC) Arthroplasty, Distal radius fracture requiring open reduction internal fixation (ORIF) and tendon repairs of the hand. Possible participants will be recruited through Cape Fear Orthopedics & Sports Medicine and receiving care from an orthopedic surgeon & hand specialist. Researchers hypothesize that those who receive the occupational therapy consult will demonstrate improved adherence with occupational therapy appointments, improved patient perceived function, and overall improved experiences with the pre-operative patient experience.

NCT ID: NCT05093946 Recruiting - Clinical trials for Flexor Tendon Rupture

Psychometric Measurement Properties of the Michigan Hand Questionnaire in Patients After Flexor Tendon Repair

Start date: December 1, 2021
Phase:
Study type: Observational

The aim of the study is to investigate the psychometric properties of the German Version of the Michigan Hand Questionnaire in patients with flexor tendon injuries, including reliability, validity and interpretability.