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Contracture clinical trials

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NCT ID: NCT03887585 Active, not recruiting - Clinical trials for Achilles Tendon Contracture

Modified Percutaneous Achilles Tendon Lengthening by Triple Hemisection for Achilles Tendon Contracture

Start date: January 1, 2010
Phase: N/A
Study type: Interventional

This study aims to evaluate the efficacy and safety of this new therapeutic method, which is based on the percutaneous sliding technique with three hemi-cuts in the tendon.

NCT ID: NCT03741764 Active, not recruiting - Clinical trials for Dupuytren Contracture

Treatment of Dupuytren's Disease With Minimal Invasive Surgery and VIVOSORB® Resorbable Implant Device

Vivosorb
Start date: December 1, 2018
Phase: N/A
Study type: Interventional

Dupuytren's disease is a progressive fibroproliferative condition of the hand which progresses in 20% of patients into a serious condition. In Flanders, Dupuytren's disease was found to be present in 32% of the population over 50 years. In severe flexion contracture finger deformity due to Dupuytren's disease, functional loss of the finger (often the fourth or fifth digit) is significant. Surgery remains the most efficient treatment for the correction of flexion deformities. Minimal invasive surgery with the creation of firebreaks for the fibrous strands causing this disease, withholds fast recovery. However, recurrence after surgery is not rare with numbers varying from 30 to 70% depending on fibrosis diathesis score of Abe, severity of the deformation and follow-up period. Numerous surgical techniques have been used for Dupuytren disease, ranging from minimally invasive surgery to subtotal preaxial amputation with skin grafting.3 In this study a well-known technique faciectomie will be performed. During this surgery a device will be inserted called VIVOSORB® VIVOSORB® is a flexible bioresorbable polymer film which is designed to separate opposing tissues throughout the critical healing process. It is very flexible facilitating the surgeon to optimally position the sheet during surgery. It is made of 100% synthetic bioresorbable material and can be used in a variety of soft tissue surgery applications. VIVOSORB® provides a barrier function enabling the tissue to regenerate without interconnective attachment. In the past cellulose, a biologic inert implant, was used for augmenting the effect of the surgical firebreaks . Cellulose has been proven to improve outcome. Nowadays, cellulose is not available for use during faciectomie surgery, since medical production has been ceased. VIVOSORB® can be a valid alternative.

NCT ID: NCT03582176 Active, not recruiting - Elbow Fracture Clinical Trials

PrEvention of Posttraumatic Joint contractuRes With Ketotifen 2

PERK2
Start date: April 26, 2019
Phase: Phase 3
Study type: Interventional

PrEvention of posttraumatic contractuRes with Ketotifen 2 (PERK 2) is a Phase III randomized, controlled, double blinded multicenter trial with 3 parallel groups (Ketotifen 2 mg or 5 mg or lactose placebo twice daily orally for 6 weeks) and a primary endpoint of elbow extension-flexion range of motion (ROM) arc at 12 weeks post-randomization.

NCT ID: NCT03407820 Active, not recruiting - Clinical trials for Carpal Tunnel Syndrome

Different Sutures in Hand Surgery

Start date: January 31, 2018
Phase: N/A
Study type: Interventional

This study aims to assess the relationship between overall satisfaction with treatment in a group of randomized patients undergoing elective hand surgery using either absorbable (4-0 Chromic) or non-absorbable (5-0 Nylon) sutures. The investigators will also assess factors associated with wound concerns, pain intensity, magnitude of limitations, and physical function within one month of surgery.

NCT ID: NCT03192020 Active, not recruiting - Clinical trials for Dupuytren Contracture

Trial Comparing Treatment Strategies in Dupuytren's Contracture

DETECT
Start date: September 15, 2017
Phase: Phase 4
Study type: Interventional

Trial is a prospective, randomized, controlled, outcome assessor-blinded, three armed parallel 1:1:1, multicenter trial. The research objective is to determine, which treatment strategy 1) primary percutaneous needle fasciotomy (PNF) followed by surgical limited fasciectomy (LF) in patients who do not respond to PNF, 2) primary collagenase clostridium histolyticym (CCH) followed by LF in patients who do not respond to CCH or 3) LF as the primary (and secondary) treatment modality is the most cost-effective in treating Dupuytren´s contracture. Short- and long-term results will be published.

NCT ID: NCT02638480 Active, not recruiting - Flexion Contracture Clinical Trials

Effectiveness of KneeMD on Flexion Contracture in Total Knee Arthroplasty Patients

KneeMD
Start date: November 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effect of the KneeMD subject-controlled knee rehabilitation device on the incidence of postoperative flexion contracture.

NCT ID: NCT01082003 Active, not recruiting - Clinical trials for Capsular Contractures

Prevention of Capsular Contracture Using Trental and Vitamin E

Start date: October 2009
Phase: N/A
Study type: Interventional

The main purpose of this research study is to determine if the use of Trental and Vitamin E will decrease the incidence and severity of contractures (shrinking and or hardening of tissue surrounding the implant) associated with breast implant reconstruction following radiation treatment. Another goal is to find out the impact that Trental and Vitamin E have on implant loss or need for surgical intervention in the setting of chest wall radiation after reconstruction. In addition, the investigators want to evaluate the patient's sense of well being and quality of life.

NCT ID: NCT01065181 Active, not recruiting - Clinical trials for Shoulder Posterior Capsular Contracture

Youth Throwers Respond to Stretching

Safethrow
Start date: January 2008
Phase:
Study type: Observational

The purpose of this study is to document the rates of youth baseball player demographics, incidence of arm pain, usage of different pitch types, and degree of internal rotation contracture in the throwing versus the non-throwing shoulder. We followed a subgroup of players for a year to see if a particular stretch would help reduce the internal rotation contracture.