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Tendon Injuries clinical trials

View clinical trials related to Tendon Injuries.

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NCT ID: NCT04110665 Recruiting - Tendon Injuries Clinical Trials

Multimodal Analgesia Strategies After Major Shoulder Ambulatory Surgery

Shoulder1
Start date: September 1, 2017
Phase: Phase 4
Study type: Interventional

This study evaluates the addition of tramadol, or nefopam or opioid to paracetamol and ketoprofene in the treatment of pain in adults after shoulder ambulatory surgery. In a first step, 30 patients will receive tramadol as rescue analgesia in combination with paracetamol and ketoprofene, while the other will receive nefopam or opioid in a sequential analysis that will be performed every 20 patients using the QoR 40 survey.

NCT ID: NCT03938935 Not yet recruiting - Clinical trials for Flexor Tendon Repair

Repair of Flexor Tendon Injuries With Eight Strand Core Stitch Without Postoperative Splinting

Start date: October 2019
Phase: N/A
Study type: Interventional

Evaluation of early active postoperative mobilisation in flexor tendon injuries without postoperative splinting

NCT ID: NCT03912168 Completed - Pain Clinical Trials

Question Prompt List for Orthopaedic Conditions

Start date: August 12, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate whether providing patients with a question prompt list (QPL) prior to their orthopaedic surgery clinic appointment improves their perceived involvement in care (PICs) score compared to being given 3 questions from the AskShareKnow model

NCT ID: NCT03880149 Recruiting - Inflammation Clinical Trials

The Effects of Omega-3 Status and Supplementation on Tendon Structure in Competitive Athletes

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

The study will examine the association between omega-3 status and the effects of omega-3 supplementation on changes in tendon structure and recovery from tendon injuries and inflammatory markers in competitive athletes. Half of the participants will receive omega-3 in combination with vitamin E, while the other half will receive a placebo and vitamin E.

NCT ID: NCT03850210 Completed - Tendon Injuries Clinical Trials

The Manchester Short Splint in the Rehabilitation of Zone II Flexor Tendon Repairs

Short Splint
Start date: June 1, 2015
Phase: N/A
Study type: Interventional

The project sets out to compare two different splints in the outcome of zone II flexor tendon injury hand therapy rehabilitation programme. Traditional hand therapy is based on using a long forearm-based splint for 6 weeks in zone II flexor tendon injuries. Manchester University NHS Foundation Trust have devised a new shorter splint to use as an alternative to the traditional longer splint as there are cogent reasons for believing that permitting more wrist movement during rehabilitation will improve the range of finger movement ultimately (tendonesis effects). Patients will be randomised to receive either the traditional long splint, or the short splint. Patients will be followed up and data will be collected at routine hand therapy appointments.

NCT ID: NCT03828916 Recruiting - Tendinopathy Clinical Trials

NuShield in Surgical Peroneal Tendon Repair

Start date: January 30, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the use of NuShield in subjects requiring surgical tendon repair.

NCT ID: NCT03823755 Completed - Clinical trials for Tendon Injury - Hand

Evaluation of the Mobility of the Digital Flexor Tendons

DynamicMRI
Start date: May 31, 2019
Phase:
Study type: Observational

To study flexor tendon excursion in the hand after surgery by dynamic MRI

NCT ID: NCT03752957 Not yet recruiting - Clinical trials for Flexor Tendon Injury

Wide-Awake Local Anesthesia For Flexor Tendon Repair

Start date: November 2018
Phase:
Study type: Observational

Primary repair for flexor tendon lacerations remain the standard of care. However, despite recent advances in knowledge of tendon healing, suture material, and post-operative protocols, outcomes have been reported as fair or poor in 7-20% of patients. Complications encountered include adhesion formation, development of joint contractures, tendon rupture, triggering, bow stringing and quadriplegia. Tendon surgery is unique because it should ensure tendon gliding after surgery Tendon surgery now can be performed under local anesthesia without tourniquet, by injecting epinephrine mixed with lidocaine, to achieve vasoconstriction in the area of surgery. This method allows the tendon to move actively during surgery to test tendon function intraoperatively and to ensure the tendon is properly repaired before leaving the operating table. Wide awake hand surgery is well described by its other name, WALANT which stands for wide awake local anaesthesia no tourniquet. The only two medications most patients are given for wide awake hand surgery are Lidocaine for anaesthesia and epinephrine for haemostasis. In the period before 1950, the belief developed among surgeons that epinephrine causes finger necrosis .The source of the epinephrine myth stemmed from the use of procaine (Novocaine). It was the only safely injectable local anaesthetic until the introduction of Lidocaine in 1948. More fingers died from procaine injection alone than from procaine plus epinephrine injection .no lost finger no case require phentolamine in many studies.

NCT ID: NCT03747198 Completed - Tendon Injuries Clinical Trials

Methylsulfonylmethane on Knee Laxity

Start date: February 1, 2019
Phase: N/A
Study type: Interventional

The proposed research will focus on determining the effect of methylsulfonylmethane (MSM) on knee laxity changes through the menstrual cycle in young active females. As an extension to recent discovery, that MSM reverses the negative effect of estrogen on engineered ligament function, the proposed work is designed to determine whether MSM can decrease the negative effect of estrogen on knee laxity in females. Ligament function is determined by the content and cross-linking of collagen, which is influenced by a milieu of biochemical and mechanical parameters. The greater the amount and cross-linking the greater the stiffness and strength of these connective tissues. In engineered ligaments it has been previously shown that the high levels of estrogen, normally present in the days before and after ovulation, can inhibit the cross-linking enzyme lysyl oxidase. This decrease in collagen cross-linking likely increases connective tissue laxity and contributes to observed 4-fold greater occurrence of anterior cruciate ligament (ACL) rupture in females. Conversely, MSM increases collagen cross-linking and recent work conducted by the Baar lab in engineered human ligaments treated with high estrogen demonstrated that MSM could completely reverse the effects of estrogen on ligament mechanics. The proposed research aims to advance this promising pre-clinical data and apply in a clinical trial. This research also proposes to quantify that knee laxity increases up to 5mm between the first day of menstruation and the day after ovulation and also that the magnitude of the increase in laxity is directly related to the magnitude of the change in estrogen. Importantly, a direct relationship between knee laxity and ACL rupture exists. For every 1.3mm increase in anterior-posterior knee displacement, the odds of ACL rupture increase 4-fold. Therefore, any treatment that decreases knee laxity could be expected to reduce ACL ruptures and have widespread application across the general active population and high-level athletics.

NCT ID: NCT03634865 Completed - Clinical trials for Radius; Fracture, Lower or Distal End

Screw Lengths in Radius Volar Plates

PESLDRF
Start date: January 25, 2018
Phase:
Study type: Observational

Background Fractures of the distal radius are among the most common. Major complications, including irritation and rupture of the extensor tendons, may occur if epiphyseal screws of inappropriate length are used. Questions/Purposes The main objective of the present study was to determine whether the optimal epiphyseal screw length can be determined by reference to the diaphyseal screw length. Methods Forty CT scans were semi-automatically segmented. A 3D model of the volar plate was affixed to each distal radius with simulation. The maximum lengths of the diaphyseal screws, as well as the four distal epiphyseal screws, were measured. Linear regression analysis was performed.