Clinical trials: Distal Radius Fracture
Distal Radius Fracture
Hematoma Block for Distal Radius Fracture
The purpose of this study is to determine the efficacy of ultrasound guided hematoma block versus traditional "blind" hematoma block for analgesia in distal radius fracture reduction.
- Trial name
- Hematoma Block (NCT02346929)
- Testing
- ultrasound guide
- Where
- United States
- Volunteers
- 115 people, healthy volunteers welcome
- Sponsor
- Beth Israel Deaconess Medical Center
Radius Fracture Distal, Pain, Postoperative
Auricular Acupuncture As Part Of A Multimodal Regimen After Distal Radius Open Reduction and Internal Fixation
This randomized controlled trial will test the hypothesis that patients receiving an intraoperative auricular acupuncture protocol will require less postoperative opioid analgesic use compared to those who do not receive…
- Trial name
- NCT05974254
- Testing
- Acupuncture
- Where
- United States
- Sponsor
- Baylor College of Medicine
Distal Radius Fracture
Immediate Mobilization Versus 2 Weeks Cast Immobilization After Distal Radius Fracture Treated With Volar Locking Plate
The aim of this study is to analyze total lenght of the sick leace and functional outcome (PRWE) at 2 months between 2 weeks casting and immediate mobilization following volar plating for a DRF.
- Trial name
- LIMPER-DRF (NCT05150925)
- Testing
- Cast treatment, Immediate mobilization, Volar plating
- Where
- 5 sites in Finland, Sweden
- Volunteers
- 240 people
- Sponsor
- Tampere University Hospital
Distal Radius Fractures
Proof-of-concept Study With NVDX3 for Treatment of Distal Radius Fractures.
Prospective, single arm, monocentric clinical study to test NVDX3 in patients suffering from distal radius fracture. NVDX3 will be implanted during a single surgical intervention.
- Trial name
- NCT05987033
- Testing
- NVDX3
- Where
- Luxembourg
- Volunteers
- 11 people
- Sponsor
- Novadip Biosciences
Complex Regional Pain Syndrome I (CRPS I), Distal Radius Fracture
Prism Adaptation Therapy for CRPS Type 1
Complex Regional Pain Syndrome (CRPS) is a clinical condition characterized by pain that arises either without an identifiable triggering factor or with a severity disproportionate to the initiating event.
- Conditions
- Complex Regional Pain Syndrome I (CRPS I), Distal Radius Fracture, CRPS (Complex Regional Pain Syndromes), Neuropathic Pain
- Trial name
- NCT07370012
- Testing
- The Prism Adaptation Therapy Group, The Control Group
- Where
- Turkey (Türkiye)
- Volunteers
- 54 people
- Sponsor
- Ankara Etlik City Hospital
Distal Radius Fracture, Casting
No Reduction Compared to Closed Reduction for Distal Radius Fractures in Patients Over 65 or Older
DISCLOSE trial is a randomized controlled trial including 532 participants with low-energy distal radius fractures. The primary objective is to evaluate whether casting without prior closed reduction is equivalent to casting…
- Conditions
- Distal Radius Fracture, Casting, Closed Reduction
- Trial name
- DISCLOSE (NCT07042139)
- Testing
- No reduction, Closed Reduction, Casting
- Where
- 10 sites in Denmark, Estonia and 2 more
- Volunteers
- 532 people
- Sponsor
- Tampere University Hospital
Distal Radius Fracture
CASTomize 4D Printed Cast Versus Fibreglass Casts for Distal Radius Fractures
This study is a randomised control trial comparing Castomize 4D printed cast versus conventional fibreglass casts in isolated conservatively treated distal radius fractures. The primary outcome measure is fracture reduction.
- Trial name
- NCT07350525
- Testing
- Castomize cast, Control
- Where
- Singapore
- Volunteers
- 25 people
- Sponsor
- Tan Tock Seng Hospital
Fracture of Distal Radius, Bone Fractures
Effectiveness of Pulsed Electromagnetic Fields and Nutraceutical Supplementation in Women With Distal Radius Fracture
This single-center randomized controlled trial tests whether adding a daily nutraceutical supplement to standard pulsed electromagnetic field (PEMF) therapy improves recovery after a recent distal radius (wrist) fracture in…
- Conditions
- Fracture of Distal Radius, Bone Fractures, Wrist Injuries
- Trial name
- NCT07352501
- Testing
- Pulsed Electromagnetic Field Therapy, Nutraceutical Supplement
- Where
- Italy
- Volunteers
- 100 people
- Sponsor
- University of Palermo
Distal Radius Fracture Fixation
Same Day Discharge Vs. Hospitalization for Operative Fixation of Distal Radius Fractures
The goal of this clinical trial is to examine the results for same-day discharge after distal radius operative fixation in adult pupolation.
- Trial name
- NCT07276334
- Testing
- early release from hospital, Day after surgery release
- Where
- Israel
- Volunteers
- 70 people
- Sponsor
- Assaf-Harofeh Medical Center
Distal Radius Fracture
Minimal Clinically Important Difference of the Push-Off Test
The aim was to determine the minimal clinically important difference of the push-off test in distal radius fractures.
- Trial name
- NCT07341594
- Testing
- Physical therapy
- Where
- Turkey (Türkiye)
- Volunteers
- 109 people
- Sponsor
- Pamukkale University
Distal Radius Fracture
Surgical Field Quality Assessment and Complications in Distal Radius Fractures Using the Minimum Inflation Tourniquet Pressure.
Analyse surgical field bleeding, surgical time, and intraoperative pain in patients undergoing osteosynthesis of distal radius fractures using ischaemia pressure calculated based on Limb Occlusion Pressure, compared with Arterial…
- Trial name
- NCT07318194
- Testing
- PNEUMATIC TOURNIQUET INFLATION PRESSURE
- Where
- Spain
- Volunteers
- 140 people
- Sponsor
- Consorci Sanitari de Terrassa
Fracture Distal Radius
Evaluating a Novel Rehabilitation Chatbot: A Pilot Randomized Controlled Trial for Distal Radius Fracture Recovery
This study is a single-center pilot randomized controlled trial evaluating a rehabilitation chatbot, "Wrist Health," for elderly patients (60-90 years) recovering from conservatively treated distal radius fractures in Hong Kong.
- Trial name
- OT FDR CHATBOT (NCT07308691)
- Testing
- Wrist Health chatbot, Conventional DRF rehabilitation
- Where
- Hong Kong
- Volunteers
- 44 people
- Sponsor
- The Hong Kong Polytechnic University
Conscious Sedation, Distal Radius Fracture
IN Dexmedetomidine for Procedural Sedation in Pediatric Closed Reductions for Distal Forearm Fractures
The primary objective of this study is to evaluate the sedative, and analgesic effects of intranasal (IN) Dexmedetomidine (DEX) in children presenting to a Pediatric Emergency Department (PED) who undergo conscious sedation for…
- Trial name
- NCT03466242
- Testing
- Dexmedetomidine, Ketamine
- Where
- United States
- Volunteers
- healthy volunteers welcome
- Sponsor
- Phoenix Children's Hospital
Fracture Forearm, Radius Distal Fracture
Distal Radial Fractures in Adult Patients: 4 Weeks Versus 6 Weeks of Cast Immobilization
Post-intervention outcomes comparing casting in distal radius fractures of four weeks versus six weeks.
- Trial name
- NCT07234370
- Testing
- Short Arm Cast for Distal Radius Fracture for four weeks, Short Arm Cast for Distal Radius Fracture for six weeks
- Where
- Pakistan
- Volunteers
- 80 people
- Sponsor
- Liaquat National Hospital & Medical College
Distal Radius Fracture, Osteoporosis
Utility of Cortical Bone Tissue Properties in the Assessment of Fracture Risk
The objective of this study is to determine whether a new minimally invasive method for in vivo measurement of cortical bone tissue properties can identify those who are at risk for fragility fractures of the hip and radius.
- Conditions
- Distal Radius Fracture, Osteoporosis, Hip Fractures
- Trial name
- NCT03076034
- Testing
- Reference Point Indentation
- Where
- United States
- Volunteers
- 190 people, healthy volunteers welcome
- Sponsor
- Beth Israel Deaconess Medical Center
Distal Radius Fractures, Wrist Fractures
Supraclavicular Bupivacaine Vs. Supraclavicular Liposomal Bupivacaine for Orthopedic Wrist Surgery
Orthopedic wrist procedures often cause significant postoperative pain. A supraclavicular nerve block is an effective and proven method to help reduce postoperative pain and decrease opioid use around the time of upper extremity…
- Trial name
- Vs (NCT06179004)
- Testing
- Liposomal bupivacaine, Bupivacaine Hydrochloride
- Where
- United States
- Volunteers
- 100 people, healthy volunteers welcome
- Sponsor
- University of North Carolina, Chapel Hill
Distal Radius Fracture Reduction, Pain Control
Pain Control Alternatives in Pediatric Patients With Distal Radius Fractures
The aim of this study is to evaluate the efficacy of a hematoma block and minimal ketamine pain control or hematoma block and intranasal fentanyl in pediatric patients presenting with distal radius fractures requiring reduction…
- Conditions
- Distal Radius Fracture Reduction, Pain Control, Pediatric Fractures
- Trial name
- NCT07120763
- Testing
- Ketamine + Lidocaine, Ketamine group, Fentanyl (Nasalfent, Fentanyl Citrate Nasal Spray)
- Where
- United States
- Volunteers
- 50 people
- Sponsor
- State University of New York at Buffalo
Distal Radius Fracture
Opiate Sparing Protocol Randomized Controlled Trial in Open Distal Radius Fracture Repair
A comparison of oral morphine equivalents between an opiate sparing cohort and an opiate based cohort following open reduction internal fixation of a distal radius fracture.
- Trial name
- NCT05215236
- Testing
- Opiate Sparing, Opiate Based
- Where
- United States
- Volunteers
- 72 people, healthy volunteers welcome
- Sponsor
- Campbell Clinic
Distal Radius Fracture, Tendon Rupture
Quantitative and Clinical Assessment of Flexor Tendon Gliding Following Application of a Bioresorbable Hydrogel: A Prospective, Randomized Study in Patients Undergoing Distal Radius Fracture Repair
The investigators will be evaluating the use of versawrap in the setting of distal radius fractures by placing membrane between plate and flexor tendons.
- Trial name
- NCT04976335
- Testing
- Versawrap membrane
- Where
- 2 sites in United States
- Volunteers
- 50 people
- Sponsor
- University of Colorado, Denver
Flexor Tendon Rupture, Thumb Osteoarthritis
Occupational Therapy Pre-operative Education in the Orthopedic Hand Setting
This will be a prospective randomized control trial with a blocking method to determine the effect of an occupational therapy focused pre-operative education on 3 pre-determined diagnosis: Carpometacarpal (CMC) Arthroplasty…
- Conditions
- Flexor Tendon Rupture, Thumb Osteoarthritis, Distal Radius Fracture
- Trial name
- NCT05095415
- Testing
- Occupational Therapy Pre-operative Consult, Typical Pre-Operative Education
- Sponsor
- Methodist University, North Carolina