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Hand Injuries clinical trials

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NCT ID: NCT04625868 Completed - Surgery Clinical Trials

Effectiveness of a Preoperative Educational Video for Reducing Opioid Consumption After Hand Surgery

Start date: May 29, 2020
Phase: N/A
Study type: Interventional

This study seeks to determine if watching a preoperative educational video influences opioid consumption and proper disposal following elective hand surgery.

NCT ID: NCT04486053 Completed - Hand Injuries Clinical Trials

Long-term Results of Pediatric Flexor Tendon Injuries

Start date: May 15, 2020
Phase:
Study type: Observational

Hand and upper extremity injuries are among the most common causes of admission of children to the emergency department since they are the most frequently injured part of body following head in pediatric and adolescent population. Although upper extremity fractures and contusions are the main reasons of pediatric hand injuries, tendon injuries are not also uncommon. There are limited data in the literature about the long-term results of children with flexor tendon injury. Therefore, the aim of this study was to evaluate the long-term functional outcomes of children with flexor tendon injury.

NCT ID: NCT04328623 Completed - Hand Injuries Clinical Trials

Interest of Hypnosis on Pain Management During a Guided Echo Infiltration of the Hand

HYMN
Start date: October 8, 2020
Phase: N/A
Study type: Interventional

Ultrasound-guided infiltration is a common procedure and is known to be locally painful. This care-induced pain leads to strong apprehension in patients who need to benefit from this procedure. The practice of hypnosis to improve the patient's comfort during a treatment has appeared progressively in hospital departments. Among the various existing conversational hypnosis techniques, there is the "magic glove" technique. This is the technique that will be used in this study. The investigators wish to evaluate the interest of hypnosis on the pain felt by the patient when performing an echo-guided infiltration of the hand, one of the most painful extremities during infiltrations.

NCT ID: NCT04215614 Completed - Clinical trials for Hand Injuries and Disorders

Lateral Sagittal vs Costoclavicular Brachial Plexus Block in Children

Start date: January 2, 2020
Phase: N/A
Study type: Interventional

Costoclavicular approach has lots of advantages compared to the lateral sagittal approach for infraclavicular brachial plexus block. Although the efficacy of this block has been demonstrated in adults, there are no randomized controlled trials in the literature on the application of pediatric patients. Our aim was to compare the ultrasound-guided infraclavicular and costoclavicular approach in pediatric patients.

NCT ID: NCT04174729 Completed - Clinical trials for Hand Injuries and Disorders

System for Quantifying the Functional Strength of the Grip and Pinch Movements

Start date: August 5, 2019
Phase: N/A
Study type: Interventional

This study developed a system to quantify the functional strength of young adults without motor impairment during grip and pinch movement. Making it possible to know the accuracy of the value of these strength, the range of motion performed and whether the grip force was maintained throughout the range of motion. In addition to checking the functionality, reliability and reproducibility of the system.

NCT ID: NCT04068506 Completed - Hand Injuries Clinical Trials

Analgesic Effects of Gabapentin and Paracetamol

GABA
Start date: September 1, 2019
Phase: Phase 4
Study type: Interventional

This research is about the effects of drug gabapentin; which is an amino acid that is structurally similar to neurotransmitter GABA. It is a novel drug used for the treatment of postoperative pain with analgesic properties having unique mechanism of action. This study reviews clinical effects of this agent in hand injury patients managed at the Department of Plastics & Reconstructive Surgery, Dow University of Health Sciences & Dr. Ruth KM Pfau Civil Hospital Karachi. This study aims to inquire the analgesic properties of gabapentin in the patients and to further investigate its comparison with the equivalent dose of paracetamol given 6 hours after undergoing operative procedure. Acetaminophen is well tolerated when administered in therapeutic dose for pain management. It is a principal drug used as pain reliever and as an antipyretic regimen. This is an experimental study in which a pre-coded questionnaire would be approved in the research for appraising the intensity of pain after intervening operative procedure using visual analogue scale, measuring the pain intensity from 0-10. The questions regarding pain intensity will be inquired after administrating the drug six hours postoperatively. The drug will be prescribed by the doctor on duty having no knowledge regarding the given drug or the group in which he/she is administrating the drug; further questionnaire will be filled by the two co-investigators who will be trained by principal investigator, how to take correct information. Sample size was calculated using www.openepi.com using the previous literature searches of similar research and 50 patients (25 in each group) will be randomly selected from the ward of a known case of hand injury. Group A patients will receive 600 mg of gabapentin post operatively while group B will receive 1 g of paracetamol for management of pain postoperatively orally.

NCT ID: NCT03865641 Completed - Hand Injuries Clinical Trials

Effects of Virtual Reality Based Rehabilitation on Burned Hands

Start date: June 28, 2019
Phase: N/A
Study type: Interventional

Hands are the most frequent injury sites caused by burn, and appropriate rehabilitation is essential to ensure that good functional recovery is achieved. Many interventions have been developed for patients with burns; however, hand rehabilitation tools are limited. Virtual reality (VR)-based rehabilitation has proven beneficial to the functions of upper and lower extremities. To investigate VR-based rehabilitation effects on burned hands, we compare the results of VR rehabilitation group to the results of matched conventional(CON) rehabilitation group.This single-blinded, randomized, controlled trial involved 31 patients with burns and dominant right-hand function impairment. Patients were randomized into a VR or a CON group. Each intervention was applied to the affected hand for 4 weeks. Hand function was evaluated using the Jebsen-Taylor hand function test (JTT), grasp and pinch power test, and Michigan Hand Outcomes Questionnaire (MHQ). These assessments were evaluated pre-intervention and 4 weeks post-intervention.Our study results suggest that VR-based rehabilitation is likely to be as effective as conventional rehabilitation for recovering hand function in a burned hand. VR-based rehabilitation may be considered a treatment option for burned hands.

NCT ID: NCT03837951 Completed - Hand Injuries Clinical Trials

Figure-of-Eight Hand, Volumetric Measurements and Reliability in Clinic With Hand Injured Patients

Start date: April 28, 2011
Phase:
Study type: Observational

This study determined the intra-rater and inter-rater reliability of the Figure-of-Eight method on healthy hands, and compared the figure-of-eight measurements to the gold standard volumetric measurements. Part B of the study conducted in a clinic, assessed the intra-rater reliability and inter-rater reliability on both hands of patients with hand injuries.

NCT ID: NCT03753295 Completed - Clinical trials for Overweight and Obesity

The Effect of BMI on Hand Grip Force in Healthy Adults

Start date: December 2, 2018
Phase:
Study type: Observational

This study will be conducted to investigate the effect of BMI on hand grip force in healthy subjects. The participants in this study will be 90 healthy subjects with right dominant lower limb (49 females and 49 males) they will be recruited from College of Applied Medical Sciences, Jazan University.

NCT ID: NCT03750045 Completed - Clinical trials for Hand Injuries and Disorders

Grip Movement Training for Adults With Fine Motor Limitation

Start date: August 1, 2016
Phase: N/A
Study type: Interventional

This study is to test the system composed by a 3D virtual environment, attached to the Leap Motion, evaluating its effects on the rehabilitation of hand movements in patients with motor alteration.