Clinical trials: Compression
Lower Extremity Lymphoedema, Leg Lymphoedema
Treatment Response to Different Lymphoedema Compression Programs Using a Pneumatic Compression Device
Proof of principle study in order to determine if there is a difference in treatment effect across the 3 study groups when treating lower extremity lymphoedema using a pneumatic compression device.
- Trial name
- NCT02031627
- Testing
- pneumatic compression - 1 hour per day, pneumatic compression - 2 hours per day, pneumatic compression - 4 hours per day
- Where
- United Kingdom
- Volunteers
- 21 people
- Sponsor
- Tactile Medical
Lymphedema of Leg, Lymphedema
A Preference Study of Two Pneumatic Compression Devices for Patients With Lower Limb Lymphedema
This study will aim to undertake a preference evaluation comparing the Aria Health Aria Free™ to a competitor's device by assessing overall satisfaction and preference of the devices individually and in comparison to one another.
- Conditions
- Lymphedema of Leg, Lymphedema, Lymphedema, Secondary, Lymphedema Primary
- Trial name
- NCT05485454
- Testing
- Aria Health Aria Free, A Traditional PCD
- Where
- United States
- Volunteers
- 20 people
- Sponsor
- ResMed
Carpal Tunnel Syndrome (CTS)
Electrophysiological and Functional Recovery After Carpal Tunnel Release
Carpal tunnel syndrome occurs when the median nerve is compressed at the wrist. It can cause pain, numbness, tingling, reduced hand strength, and difficulty performing daily activities.
- Trial name
- ELECTRO-CTS (NCT07803939)
- Testing
- Primary Carpal Tunnel Release Surgery
- Volunteers
- 100 people
- Sponsor
- Istanbul Medipol University Hospital
Compression Fracture of Thoracic Vertebral Body, Spinal Compression Fracture
Dual-energy CT in Detecting Bone Marrow Edema of Vertebral Compression Fractures
The purpose of this study is to 1. Assess bone marrow edema within the VCF by use of a DE CT virtual noncalcium image compared with MR imaging as standard reference. 2.
- Trial name
- NCT01281826
- Where
- Taiwan
- Volunteers
- 70 people
- Sponsor
- National Cheng-Kung University Hospital
Lymphedema Lower Extremity
Assessment of the Efficacy of the Dynamic Decongestive System in the Intensive Phase of Lower Limb Lymphedema
The goal of this study is to compare the efficacy of a dynamic compression device (DDS) with traditional multicomponent bandages (TMCB) in terms of excess volume reduction in lower limb lymphoedema during the first 5 days of…
- Trial name
- EDYDES-int (NCT07622615)
- Testing
- Control group: Traditional multicomponent bandages, DDS group: Dynamic compression device (DDS)
- Where
- 3 sites in France, Germany
- Volunteers
- 110 people
- Sponsor
- Jean-Paul Belgrado
Forearm Fractures
Management of Diaphyseal Forearm Fractures in Adolescents
evaluate and compare the clinical, and radiographic outcomes of 2.7 mm locking compression mini-plate osteosynthesis versus titanium elastic intramedullary nail (TEN) in the surgical management of diaphyseal fractures of both…
- Trial name
- NCT07705347
- Testing
- Open reduction and internal fixation, Closed or mini-open reduction and fixation
- Where
- Egypt
- Volunteers
- 20 people
- Sponsor
- Sohag University
Dry Needling, Carpal Tunnel Syndrome
Dry Needling and Rehabilitatin Carpal Tunnel Syndrome
Dry needling is used for myofascial release. However, its effectiveness in carpal tunnel syndrome (CTS) is not well known. It is thought that dry needling may also be an effective treatment for CTS by providing relaxation in the…
- Conditions
- Dry Needling, Carpal Tunnel Syndrome, Myofacial Pain
- Trial name
- NCT06358326
- Testing
- Dry needling, Control group
- Where
- Turkey (Türkiye)
- Volunteers
- 78 people, healthy volunteers welcome
- Sponsor
- Karabuk University
Carpal Tunnel Syndrome
Preoperative Antibiotics for Carpal Tunnel Release Surgery
This is a clinical trial to determine how effective antibiotics administered prior to endoscopic carpal tunnel release surgery are in preventing surgical site infections.
- Trial name
- NCT03432858
- Testing
- Vancomycin, Cefazolin, Saline Solution
- Where
- United States
- Volunteers
- 184 people
- Sponsor
- WellSpan Health
Hypermobility Type Ehlers-Danlos Syndrome
Compression Garments on Hypermobility Type of Ehlers-Danlos Syndrome (CGhEDS)
This study evaluates the effects of wearing a compression garment on the postural balance of patients with hypermobility type of Ehlers-Danlos syndrome, in randomised controlled study.
- Trial name
- VECO (NCT03359135)
- Testing
- Rehabilitation, Compression Garment
- Where
- France
- Volunteers
- 40 people
- Sponsor
- Hôpital Raymond Poincaré
Orthognathic Surgery, Postoperative Pain
Kinesio Taping vs Rigid Compression Taping Following Bimaxillary Orthognathic Surgery
Postoperative facial swelling and pain are common complications following corrective jaw surgery (bimaxillary orthognathic surgery).
- Conditions
- Orthognathic Surgery, Postoperative Pain, Edema
- Trial name
- NCT07833540
- Testing
- Kinesio Taping, Rigid Compression Taping
- Where
- Turkey (Türkiye)
- Volunteers
- 36 people
- Sponsor
- Gazi University
Ankle Fractures
Compression in Anklefracture Treatment, The CAT-study
The aim of this project is to find out if compression treatment can lower the incidens of surgical wound complications, such as infection and wound rupture, in patients with ankle fractures.
- Trial name
- CAT (NCT02481076)
- Testing
- Flowtron Hydroven and Coban2 Lite, Braun frame, compression bandage
- Where
- Denmark
- Volunteers
- 156 people
- Sponsor
- Hillerod Hospital, Denmark
Thoracic Outlet Syndrome
Motivational Interviewing in Thoracic Outlet Syndrome
The goal of this clinical trial is to learn if motivational interviewing (MI) works to improve symptoms in people with thoracic outlet syndrome (TOS).
- Trial name
- NCT07668206
- Testing
- Motivational Interviewing, Home Exercise Program
- Where
- Turkey (Türkiye)
- Volunteers
- 70 people
- Sponsor
- Hacettepe University
Cellulite
Does Cell-U-Light Apparel Improve Cellulite
This trial is arranged in 3 stages, lasting 8 weeks overall, designed to assess the before, during and after effects of the low-compression apparel with its integrated, variably raised, ink-polymer pads.
- Trial name
- NCT05748678
- Testing
- Compression pants
- Where
- United Kingdom
- Volunteers
- 24 people, healthy volunteers welcome
- Sponsor
- The Whiteley Clinic
Osteoporosis
Percutaneous Vertebroplasty Versus Conservative Treatment in GIOPVCF
Based on the case reports and other literature, the investigators hypothesize that using PVP for treating GIOPVCF is associated with increased risk of vertebral refractures and does not provide further benefits compared to…
- Trial name
- NCT03330340
- Testing
- Percutaneous Vertebroplasty
- Volunteers
- 106 people
- Sponsor
- Peking University First Hospital
Covid19, Thrombosis
Enoxaparin at Prophylactic or Therapeutic Doses in COVID-19
SINGLE CENTER PHASE III INTERVENTIONAL RANDOMIZED CONTROLLED TRIAL comparing efficacy and safety of enoxaparin at prophylactic dose (standard treatment) and enoxaparin at therapeutic dose (OFF-LABEL treatment) in 300 COVID-19…
- Trial name
- EMOS-COVID (NCT04646655)
- Testing
- Enoxaparin
- Where
- Italy
- Volunteers
- 142 people
- Sponsor
- ASST Fatebenefratelli Sacco
Carpal Tunnel Syndrome
Different Sessions of Perineural Injection With Dextrose for Carpal Tunnel Syndrome
Carpal tunnel syndrome (CTS) is the most common peripheral entrapment neuropathy with involving compression of the median nerve in the carpal tunnel.
- Trial name
- NCT03802435
- Testing
- two-sessions of ultrasound-guided PIT, One-sessions of ultrasound-guided PIT
- Where
- Taiwan
- Volunteers
- 30 people, healthy volunteers welcome
- Sponsor
- Tri-Service General Hospital (TSGH)
Macular Holes
Air Tamponade and Non-supine Positioning in Macular Hole Surgery.
This is a prospective, multicenter, randomized non-inferiority trial, where the macular hole closure rate with intraocular air tamponade is compared to the closure rate with gas tamponade.The patients are randomized to receive…
- Trial name
- NCT03572725
- Testing
- Gas tamponade, Air tamponade
- Where
- 5 sites in Norway
- Volunteers
- 150 people
- Sponsor
- Helse Stavanger HF
Providing Sufficient Cerebral Oxygenation During CPR
Chest Compression and Cerebral Oxygenation During Cardiopulmonary Resuscitation
In recent years, monitorizations during Cardiopulmonary Resuscitation (CPR) are inadequate to show the sufficiency of cerebral oxygenation.
- Trial name
- CPR (NCT03062306)
- Where
- Turkey (Türkiye)
- Volunteers
- 20 people
- Sponsor
- Nevsehir Public Hospital
Carpal Tunnel Syndrome (CTS)
NeuroPath Comparative Validation Study Plan
The purpose of the study is to compare the performance of the NeuroPath automated nerve conduction test with the standard of care manual test in the diagnosis of entrapment neuropathies.
- Trial name
- NCT00393549
- Testing
- NeuroPath
- Where
- 2 sites in United States
- Volunteers
- 200 people, healthy volunteers welcome
- Sponsor
- Excel-Tech Ltd.
Respiration, Artificial, Critical Care
Pressure Support During Chest Wall Compression
The purpose of this study is to compare two physiotherapy techniques: chest wall compression versus chest wall compression plus increase of 10 cmH2O in inspiratory pressure.
- Trial name
- NCT01155648
- Testing
- Chest wall compression plus increase of 10 cmH2O in inspiratory pressure during Pressure Support Ventilation for ten minutes in chest., Chest wall compression for ten minutes in chest
- Where
- Brazil
- Volunteers
- 66 people
- Sponsor
- Hospital de Clinicas de Porto Alegre
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