Clinical Trials Logo

Trigger Finger Disorder clinical trials

View clinical trials related to Trigger Finger Disorder.

Filter by:

NCT ID: NCT04645303 Recruiting - Trigger Finger Clinical Trials

Injection of Hyaluronic Acid Versus Corticosteroid for Treatment of Trigger Finger

Start date: November 6, 2020
Phase: Early Phase 1
Study type: Interventional

The aim of the study is to compare the therapeutic effects of hyaluronic acid versus steroid injections in treating trigger fingers using ultrasound guidance

NCT ID: NCT04253457 Recruiting - Clinical trials for Carpal Tunnel Syndrome

The SToICAL Study - The Soft Tissue Injection of Corticosteroid And Local Anaesthetic Study

SToICAL
Start date: February 26, 2020
Phase: Phase 3
Study type: Interventional

Some hand conditions can be treated with a steroid injection. Some doctors mix the steroid with local anaesthetic in the hope that the patient will experience less pain after the injection. Some doctors do not do this. It is not known if adding local anaesthetic to the steroid improves patient's pain after the injection. The overall aim of the study is to see whether using local anaesthetic in the steroid injection makes a difference to patients' pain. If the study shows that using local anaesthetic improves patients' pain then the investigators should continue using it. If not, the investigators should stop giving patients unnecessary medication, which would also save the NHS time and money.

NCT ID: NCT04167098 Recruiting - Tendon Entrapment Clinical Trials

Effectiveness of Platelet-rich Plasma for Treatment of Trigger Finger

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

Study purpose is to evaluate the effectiveness of Platelet-rich Plasma (PRP) injection in the treatment of trigger finger. We compare PRP to a corticosteroid (methylprednisolone) injection in a prospective randomized triple-blind placebo-controlled study. Patients with clinically confirmed trigger finger are randomized (1:1:1 computer generated sequence with random block size) to three parallel groups and will receive an injection of either PRP, corticosteroid or placebo (0.9% saline) around the affected tendon sheath in a double-blind setting. Baseline data is collected and is followed by a phone call at 1 month, and follow-up visits at 3, 6, 12 and 24 months after the intervention. Unveiling of the allocation is at 6 months post-intervention. The primary outcome measures are: - Symptom resolution - Patient-Rated Wrist Evaluation Secondary outcomes: - Quick-Disabilities of the Arm, Shoulder and Hand - Pain Visual Analogue Score - Global improvement (7-step Likert-scale) - Grip strength - Finger range of motion

NCT ID: NCT03928873 Recruiting - Trigger Finger Clinical Trials

Extracorporeal Shock Wave in the Treatment of Trigger Finger

Start date: February 20, 2019
Phase: N/A
Study type: Interventional

Trigger finger (TF) is a condition that causes triggering, snapping, or locking on flexion of the involved finger, with a life- time risk between 2%-3% in the general population. A variety of treatments have been described, but the most effective treatment for this common disorder is still under debate. Recently, extracorporeal shock wave therapy(ESWT) has been advanced as a possible alternative to surgery for the treatment of musculoskeletal disorders in patients recalcitrant to traditional conservative treatment. However, the effectiveness of ESWT on the treatment of TF is still in lack of evidence. The purpose of this study is to conduct a prospective randomized clinical trial to compare the efficacies of ESWT at two different energy flux density with placebo treatment for the management of TF. The investigators intended to enrolled 60 participants randomly allocated to three groups: low energy ESWT (1500 impulses and 0.006mJ/mm2, 3bar, once per week for 4 weeks), high energy ESWT (1500 impulses and 0.01mJ/mm2, 5.8bar, once per week for 4 weeks) or placebo treatment groups. The effectiveness of the treatment will be assessed using cure rates, a visual analogue scale, the frequency of triggering, the severity of triggering, the functional impact of triggering, and the Quick-Disabilities of the Arm, Shoulder, and Hand questionnaire (qDASH) at 1, 3, and 6 months after treatment. An intention-to-treat analysis will be used in this study. The investigators intend to determine the efficacy of ESWT in the treatment of TF and to find out the ideal energy set-up of ESWT for TF treatment.

NCT ID: NCT03790969 Recruiting - Trigger Finger Clinical Trials

Minimizing Pain Experience In Trigger Finger Steroid Injection.

Start date: January 15, 2019
Phase: N/A
Study type: Interventional

To study the pain experience of trigger finger steroid injection with 26 gauge needle as compared to 23 gauge needle.

NCT ID: NCT03781141 Recruiting - Clinical trials for Carpal Tunnel Syndrome

Wound Closure Study in Carpal Tunnel and Trigger Finger Surgery

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

Does a difference in patient satisfaction and cosmetic outcome exist between wound closure with absorbable or non-absorbable sutures.

NCT ID: NCT03156829 Recruiting - Trigger Finger Clinical Trials

Effectiveness of Cortisone Injection and Splinting for Trigger Finger

Start date: November 27, 2017
Phase: Phase 4
Study type: Interventional

Trigger finger has a prevalence rate of up to 3%. There are many approaches available to manage this condition. While corticosteroid injection is widely accepted as the most common first-line treatment, its superiority over splint treatment has not been established. This study aims to test the effectiveness of cortisone injections, splint and cortisone+splint to resolve symptoms.

NCT ID: NCT03131882 Recruiting - Trigger Digit Clinical Trials

Efficacy of Ultrasound Guided Hyaluronic Injection in Treatment of Trigger Finger

Start date: October 1, 2016
Phase: Phase 2/Phase 3
Study type: Interventional

Comparing the Efficacy of Ultrasound Guided Hyaluronic Injection with Ultrasound Guided Corticosteroid Injection in Treatment of Trigger Finger

NCT ID: NCT00951236 Recruiting - Trigger Finger Clinical Trials

Study Comparing One Versus Two Cortisone Injections for Trigger Finger

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

Trigger finger, also known as stenosing tenosynovitis, is a painful condition that can cause discomfort and disability. Many physicians choose to locally inject cortisone into the infected finger although there is no current consensus as to how many injections are needed to achieve maximum relief. This study will be a prospective, randomized study to compare one versus two injections for the treatment of trigger finger.