Clinical Trials Logo

Hand Injuries clinical trials

View clinical trials related to Hand Injuries.

Filter by:

NCT ID: NCT02641613 Completed - Hand Injury Clinical Trials

Retroclavicular Versus Supraclavicular Brachial Plexus Block for Hand and Forearm Surgery

Start date: January 2016
Phase: Phase 4
Study type: Interventional

Patients will be randomized to one of two groups: 1. Supraclavicular group: supraclavicular brachial plexus block performed with the aid of ultrasound; 2. Retroclavicular group: retroclavicular brachial plexus block performed with the aid of ultrasound.

NCT ID: NCT02630290 Completed - Hand Injuries Clinical Trials

Addition of Dexmedetomidine to Ropivacaine-induced Supraclavicular Block (ADRIB Trial)

ADRIB
Start date: December 2015
Phase: Phase 4
Study type: Interventional

Dexmedetomidine, an alpha 2-adrenoreceptor agonist, has been found to exerts an excellent influences on the filed of perineural block. It could shorten the onset time and prolong the duration of the nerve block and improved postoperative pain. However, Dexmedetomidine-induced bradycardia or hypotension has recently attracted considerable attention because of potentially grave consequences, including sinus arrest and refractory cardiogenic shock. A low dose may help minimize cardiovascular risks associated with dexmedetomidine. However, few studies have addressed the clinical effects of low-dose dexmedetomidine as an perineural adjuvant. The present study was designed to test the hypothesis that low-dose dexmedetomidine added to ropivacaine would safely enhance the duration of analgesia without adverse effects when compared with ropivacaine alone. Investigators will conduct a single-center, prospective, randomized, triple-blind, controlled trial in patients undergoing elective forearm and hand surgery under ultrasound-guided supraclavicular brachial plexus block using either ropivacaine or ropivacaine plus low-dose dexmedetomidine. The primary outcome is self-reported duration of analgesia . Secondary outcomes include onset time and duration of motor and sensory block, total postoperative analgesics, and safety assessment (adverse effects and postoperative abnormal sensation).

NCT ID: NCT02465840 Completed - Hand Injury Clinical Trials

Hand Injury Patients Receiving Different Rehabilitation Programs

Start date: August 2016
Phase: N/A
Study type: Interventional

Hand injury is one of common occupational or traumatic injury at outpatient clinic of rehabilitation department. The motor or sensory deficits after hand trauma including bony fracture,tendon / nerve injury, joint stiffness, motion restriction, sensory impairment, or pain lead to impaired upper extremity function, ability for daily activity, or quality of life. Rehabilitation is a kind of therapy for disability after hand trauma. It could provide pain control, improvement of joint motion, stiffness reduction, preventing secondary trauma. The investigators consider that there are some deficits in hand function and range of motion, pain after injury, and some attenuation of brain functional MRI (fMRI) for hand motor control. Therefore, optimal and early intervention of rehabilitation programs may have some benefits for their hand functional outcome and improve the brain activities in fMRI images for the hand motor control. The aims of this study are to compare the differences in hand motor control area of brain functional MRI (fMRI) between normal subjects and hand injury patients before treatment and to investigate the improvement in brain fMRI activity and functional outcome after early rehabilitation in hand injury patients. The investigators will collect 40 patients with hand trauma after operation and 10 normal subjects in this study. The 10 normal subjects were allocated in the control group. These 40 patients were randomly divided into 2 experimental groups: 20 patients in group A and 20 patients in group B. In group A and B, the patients will perform immobilization and Kleinert programs respectively. All patients will perform rehabilitation regimen with 2-3 sessions per week for 3-6 months. Before and after rehabilitation, all patients will receive physical examinations, brain fMRI, and DASH questionnaire for daily activity.

NCT ID: NCT02459847 Completed - Hand Injuries Clinical Trials

Mind-Body Training for Hand Rehabilitation

Start date: August 2014
Phase: N/A
Study type: Interventional

The objectives of this pilot study are to: (1) evaluate acute effects of biofeedback and mindfulness training on pain, anxiety, and stress during a hand therapy visit and (2) gain understanding of patient perceptions, preferences, and experiences with mind-body interventions.

NCT ID: NCT02331004 Completed - Hand Injuries Clinical Trials

Effectiveness of an Intervention Program for Fine Motor Skills

Start date: May 2014
Phase: N/A
Study type: Interventional

Investigators have created a protocol of intervention to treating the general disability of upper limbs.

NCT ID: NCT02112006 Completed - Hand Injury Clinical Trials

Comparing Two Injection Sites of Local Anesthetic for Hand Surgery

Start date: April 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to compare two different injection sites for local anesthesia in patients having hand surgery. The hypothesis is that subjects receiving injections around the three nerves of the forearm will provide faster pain control and greater patient satisfaction than patients having one injection closer to the shoulder.

NCT ID: NCT01611064 Completed - Clinical trials for Hand Injuries/Disease Requiring Surgery to the Hand

A Study Investigating Ways to Make Local Anaesthetic Hand Surgery Less Painful - Reducing Tourniquet Associated Pain

ReTAP
Start date: February 2012
Phase: N/A
Study type: Interventional

Hand surgery requires a reduced blood flow to the hand during the operation, which is achieved using a tourniquet (tightly inflated circumferential cuff) around the upper arm. However this tourniquet is painful. This study investigates whether breathing oxygen can reduce the pain associated with the tourniquet to both improve patient experience and potentially to allow longer operations to be completed under a local anaesthetic (rather than a general anaesthetic, where the patient is put to sleep, which is more costly, time consuming and risky for the patient).

NCT ID: NCT01210833 Completed - Hand Injuries Clinical Trials

Using HandTutor With Traumatic Hand Injuries: Characterizing the System

Start date: October 2010
Phase: N/A
Study type: Interventional

HandTutor is a computerized system designed to evaluate and rehabilitate hand function. It is composed of a glove with optic sensors detecting the movements of the wrist and the fingers with a biofeedback software designed to evaluate and then to exercise the hand movements through supplying a variety of computer graphic patterns. The HandTutor has been used and tested with a stroke population, and it seems potential to be used with hand injuried population. As a first step, it is important to investigate the characteristics of the system and how it is matching the hand injuried population. The purpose if this study is to characterize the HandTuror system and the focused objectives are: 1. To examine the test-retest reliability of the system when measuring the range of motion (ROM) of the the fingers among healthy people (control group). 2. To examine the correlation between the ROM measured by the HandTutor and the ROM measured by conventional assessment tools (goniometer). 3. To examine the ability of the system to distinguish between healthy people and hand injured people. 4. To examine the correlation between the performance in the HandTutor (in the games part), and the performance in functional activities. 5. To examine the participants feedback for using the HandTutor (degree of enjoyment).