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Tendinopathy clinical trials

View clinical trials related to Tendinopathy.

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NCT ID: NCT06252389 Not yet recruiting - Clinical trials for Achilles Tendon Rupture

Degenerative Achilles Tendon Rupture Repair With Regeneten Augmentation

Start date: February 1, 2025
Phase:
Study type: Observational

Retrospective Case Series to investigate the effect a bovine collagen patch to augmented repair in acute Achilles tendon rupture with pre-existing tendinopathy

NCT ID: NCT06241404 Completed - Clinical trials for Shoulder Tendinopathy

Efficacy of Therapeutic Exercise vs. Treatment of Myofascial Trigger Points.

Start date: October 1, 2023
Phase: N/A
Study type: Interventional

Background: Shoulder pain commonly affects the general population, with rotator cuff tendinopathy being the most common cause. the most common cause, with rotator cuff tendinopathy diminishing function and quality of life, leading to a major socio-economic impact. quality of life, leading to a major socio-economic impact. As a result, there are two treatment approaches with potential effectiveness: therapeutic exercise (TE) and myofascial trigger point treatment (TMT). trigger point treatment (TTP). Objective: The main objective of this randomised clinical trial is to determine the efficacy of ET versus treatment of MTPs in shoulder tendinopathies. Methods: For this study, 20 participants were randomly divided into two groups: a ET group, with which a 10-exercise programme was initiated (n = 10), and a PGM group which was given an intervention protocol (n = 10). intervention protocol (n = 10). Both received a total of 10 sessions. Pain intensity pain intensity, pressure pain threshold (PPT) and range of motion (ROM) were assessed before starting and after 10 sessions. and after 10 sessions.

NCT ID: NCT06222710 Recruiting - Clinical trials for Pharmacological Action

Ultrasound Guiding Pharmacopuncture Therapy for Supraspinatus Tendinopathy

Start date: December 20, 2023
Phase: N/A
Study type: Interventional

The purpose of this study is to confirm the comparative effect and accuracy of ultrasound procedures by conducting a practical randomized controlled clinical study comparing patients (20 patients) with ultrasound-guided pharmacoacupuncture and patients (20 patients) without checking ultrasound images in 40 patients with whom complain of moderate or higher pain with 5 or higher NRS when stabilizing the shoulder joint.

NCT ID: NCT06217432 Recruiting - Tendinopathy Clinical Trials

A Study of the Effect of Time-of-day of Training on Chronic Patellar Tendinopathy

TENDOTIME
Start date: January 10, 2024
Phase: N/A
Study type: Interventional

The study is a 12-week human study where 60 participants with chronic patellar tendinopathy (more than 3 months symptoms duration) are randomised to undergo 12 weeks of targeted resistance exercise either in the morning or in the late afternoon. The overall aim is to investigate when the best time of the day to perform muscular strength training therapy towards tendinopathy is. The study will also include 10 healthy controls who will not perform any exercise training.

NCT ID: NCT06199583 Completed - Clinical trials for Patellar Tendinopathy

Diagnostic Value of Shear-Wave Elastography for Patellar Tendinopathy

Start date: August 17, 2020
Phase:
Study type: Observational

To investigate the accuracy of shear-wave elastography (SWE) in diagnosing patellar tendinopathy in female volleyball and basketball players. In addition, we want to compare different parts of the patellar tendon and investigated the effects of different knee angles.

NCT ID: NCT06172218 Recruiting - Clinical trials for Achilles Tendinopathy

AM for Refractory Achilles Tendinopathy

Start date: November 22, 2023
Phase: N/A
Study type: Interventional

To evaluate outcomes after use of micronized amniotic membrane to replace or supplement damaged or inadequate integumental tissue in patients with "chronic" insertional or non-insertional Achilles tendinopathy that remains refractory to standard care. Outcomes between a control and treatment group in this pilot study will be used to devise a multi-center study with larger sample size.

NCT ID: NCT06171555 Enrolling by invitation - Tennis Elbow Clinical Trials

Efficacy of CTM for Tennis ELbow

Start date: January 26, 2023
Phase: Phase 2
Study type: Interventional

In this study, the objective is to evaluate the effectiveness of a single application of human Connective Tissue Allograft (CTA) as a treatment of LET. CTM Biomedical markets and distributes decellularized particulate human placental connective-tissue matrix products, intended solely for homologous use to supplement or replace damaged or inadequate connective-tissue. These are structural tissue allografts processed according to the criteria contained in 21CFR 1271.10(a) for regulation solely under section 361 of the Public Health Service Act. Drug/Device Handling: If the research involves drugs or device, describe your plans to store, handle, and administer those drugs or devices so that they will be used only on subjects and be used only by authorized investigators.

NCT ID: NCT06160427 Recruiting - Shoulder Pain Clinical Trials

Connective Tissue Matrix for Rotator Cuff Tendinopathy

Start date: December 4, 2023
Phase: Phase 4
Study type: Interventional

The purpose of this research study is to determine if the effectiveness of a single injection of CTM Boost in the treatment of patients with rotator cuff tendinopathy (RCT) is as effective as a single injection of platelet rich plasma (PRP) in reducing the symptoms of RCT.

NCT ID: NCT06150378 Completed - Clinical trials for Shoulder Tendinopaty

Comparison Between Platelet Rich Plasma and Corticosteroids for the Treatment of Rotator Cuff Tendinopathy

Start date: September 30, 2022
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to test if Plateth-rich plasma would provide improved pain relief and function in patients with rotator cuff tendinopathy compared to standard treatment of corticosterone injections. Researchers will compare a control group of patients treated with a corticosterone injection with a case group of patients treated with Plateth-rich plasma injection. The purpose of this study is to perform a double-blind randomized controlled trial, comparing PRP with corticosteroids to provide pain relief and improve function in patients with rotator cuff tendinopathy. The hypothesis of this study is that PRP would provide improved pain relief and function in patients with rotator cuff tendinopathy compared to standard treatment of CS injections.

NCT ID: NCT06148805 Recruiting - Shoulder Tendinitis Clinical Trials

Effect of Pilates Exercises and Diaphragm Manual Therapy Techniques in Rotator Cuff Tendinopathy

Start date: October 1, 2023
Phase: N/A
Study type: Interventional

1. To investigate the effect of Pilates exercises program on pain intensity, pain threshold, shoulder lateral rotator strength, abduction strength and shoulder function in patients with (RCT). 2. To investigate the effect of diaphragm manual therapy techniques on pain intensity, pain threshold, shoulder lateral rotator strength, abduction strength and shoulder function in patients with (RCT). 3. To determine the effect of combination between Pilates exercises program and diaphragm manual therapy techniques on pain intensity, pain threshold, shoulder lateral rotator strength, abduction strength and shoulder function in patients with (RCT).