Clinical trials: Upper Limb Surgery
Surgery
Digital Prehabilitation for Patients Undergoing Major Elective Surgery
Prehabilitation describes the process of improving someone's functional capacity before major surgery. Prehabilitation commonly focuses on exercise training, as fitness level is a predictor of surgical outcomes - the fitter you…
- Trial name
- NCT06137781
- Testing
- Six weeks of digital prehabilitation
- Where
- 2 sites in United Kingdom
- Volunteers
- 35 people
- Sponsor
- Royal United Hospitals Bath NHS Foundation Trust
Anesthesia, Regional Anesthesia Morbidity
Motor Sparing Supraclavicular Block
This study aims to compare MS-SCBPB and SCBPB in the duration of postoperative analgesia, time to first analgesic request (VAS ≥40 mm), pain scores, motor power, and side effects.
- Trial name
- NCT06074471
- Testing
- ultrasound guided supraclavicular brachial plexus block
- Where
- Egypt
- Volunteers
- 44 people
- Sponsor
- Cairo University
Blood Loss, Surgical
Effect of Aprotinin on Transfusion Requirements and Blood Loss in Patients Undergoing Elective Primary Total Hip Replacement
The purpose of this study is to assess if aprotinin (BAY A0128), given intravenously during surgery, is safe and can help reduce the amount of bleeding and the need for a blood transfusion during hip replacement surgery.
- Trial name
- NCT00668031
- Testing
- Trasylol (Aprotinin, BAYA0128)
- Where
- 40 sites in United States, Canada and 1 more
- Volunteers
- 359 people
- Sponsor
- Bayer
Procedural Sedation
A Safety Study of AQUAVAN® (Fospropofol Disodium) Injection for Sedation During Minor Surgical Procedures.
Very often patients receive medications before a diagnostic, therapeutic, or surgical procedure to help them relax, keep them calm, and to relieve them from pain. This is called procedural sedation.
- Trial name
- NCT00327392
- Testing
- AQUAVAN® (fospropofol disodium) Injection
- Where
- 15 sites in United States
- Volunteers
- 123 people
- Sponsor
- Eisai Inc.
Apicomarginal Defects
Healing of Apicomarginal Defects Using Autograft or Allograft With Collagen Membrane
Apicomarginal defects, which connect apical and marginal bone loss, are difficult to manage surgically due to their limited regenerative potential.
- Trial name
- NCT07412067
- Testing
- Guided tissue regeneration
- Where
- India
- Volunteers
- 50 people
- Sponsor
- Postgraduate Institute of Dental Sciences Rohtak
Neuroendocrine Tumors
Neoadjuvant PRRT With 177Lu-DOTATATE Followed by Surgery for Resectable PanNET
Peptide Receptor Radionuclide Therapy (PRRT) is based on specific somatostatin receptor targeting with radiolabelled analogues 90Y-DOTATOC and 177Lu-DOTATATE.
- Trial name
- NeoLuPaNET (NCT04385992)
- Testing
- 177Lu-Dotatate
- Where
- Italy
- Volunteers
- 31 people
- Sponsor
- IRCCS San Raffaele
Cerebrospinal Fluid Leak
Evaluate the Safety and Performance of Dura Sealant Patch in Reducing CSF Leakage Following Elective Cranial Surgery
The objective of the study is to clinically assess the safety and performance of the Dura Sealant Patch as a means of reducing intra- as well as post-operative CSF leakage in patients undergoing elective cranial intradural…
- Trial name
- NCT03566602
- Testing
- Dura Sealant Patch
- Where
- 3 sites in Netherlands, Switzerland
- Volunteers
- 40 people
- Sponsor
- Polyganics BV
Malignant Melanoma, Metastases
Buparlisib in Melanoma Patients Suffering From Brain Metastases (BUMPER)
The study will enrol adult female and male patients with BRAF wild-type melanoma and brain metastases who are not eligible for surgery or radiosurgery and failed prior therapy with ipilimumab, and patients with BRAF V600…
- Trial name
- BUMPER (NCT02452294)
- Testing
- Buparlisib
- Where
- 2 sites in Germany
- Volunteers
- 22 people
- Sponsor
- University Hospital Tuebingen
Hand Injuries and Disorders, Distal Radius Fracture
The Role of Tranexamic Acid in Reducing Post Operative Hand Edema After Hand and Wrist Surgery
Hand edema following hand surgery is a common yet devastating side effect that can lead to early stiffness, prolonged rehabilitation and diminished function.
- Conditions
- Hand Injuries and Disorders, Distal Radius Fracture, Dupuytren Contracture
- Trial name
- THAW (NCT04907812)
- Testing
- Tranexamic acid, Surgery
- Where
- Canada
- Volunteers
- 50 people
- Sponsor
- Ruby Grewal
Muscle-Invasive Bladder Carcinoma, Programmed Cell Death Protein 1 Inhibitor
Treating Muscle-invasive Bladder Cancer With A Non-surgical Method Consisting of Anti-PD-1 Therapy and Chemoradiation
The goal of this Phase 2 trial is to evaluate a non-surgical bladder-preserving treatment mode which consists of neoadjuvant chemotherapy plus anti-programmed cell death protein 1 (anti-PD-1) therapy followed by radiotherapy plus…
- Conditions
- Muscle-Invasive Bladder Carcinoma, Programmed Cell Death Protein 1 Inhibitor, Radiotherapy
- Trial name
- BCIRT-01 (NCT05975307)
- Testing
- Toripalimab, Gemcitabine, Cisplatin
- Where
- China
- Volunteers
- 64 people
- Sponsor
- Sun Yat-sen University
Rotator Cuff Tear
Prospective Study for Safety and Efficacy of InSpace™ in Rotator Cuff Tear Subjects
Title: One-arm, international, multi-center with competitive recruitment, prospective study to assess the safety and efficacy of OrthoSpace's InSpace™ in rotator cuff tear subjects scheduled for surgery of the rotator cuff - A…
- Trial name
- NCT00916994
- Testing
- SpaceGuard Balloon
- Where
- Israel
- Volunteers
- 58 people
- Sponsor
- OrthoSpace Ltd.
Radius Fracture
Distal Radial Fractures in the Late Middle Aged
Background: Wrist fractures are a common injury among people aged 55-70. The radius is one of the bones making up the wrist joint, and is typically the site of injury in a broken wrist.
- Trial name
- RIST (NCT02353338)
- Testing
- Surgical intervention, Conservative management, cast
- Where
- Canada
- Volunteers
- 51 people, healthy volunteers welcome
- Sponsor
- University of Alberta
Distal Humerus Fracture
Retrospective Analysis on Distal Humerus Fractures
The purpose of this study is to evaluate preoperative objective measurements for distal humerus ORIF patients and operative objective measurements to determine if there is any effect to postoperative outcomes.
- Trial name
- (DHFx) (NCT03637621)
- Testing
- ORIF
- Where
- United States
- Volunteers
- 60 people, healthy volunteers welcome
- Sponsor
- The Orthopaedic Research & Innovation Foundation
Rotator Cuff Injuries, Shoulder Disease
Feasibility of an Analgesic Device Enabling Local Anesthetic Delivery and Neuromodulation After Shoulder/Foot Surgery
Postoperative pain remains undertreated with inadequate analgesic options. Opioids have well-known limitations for both individuals and society; single-injection and continuous peripheral nerve blocks provide intense analgesia…
- Conditions
- Rotator Cuff Injuries, Shoulder Disease, Hallux Valgus, Ankle Arthropathy
- Trial name
- NCT06818708
- Testing
- Experimental Treatment
- Where
- United States
- Volunteers
- 20 people
- Sponsor
- University of California, San Diego
Healthy
Timing of Subcutaneous Tranexamic Acid Injection in Mohs Micrographic Surgery
This study will compare postoperative bleeding after subcutaneous tranexamic acid (TXA) is administered during Mohs surgery either after tumor clearance and before reconstruction or after reconstruction and before bandage…
- Trial name
- NCT07807371
- Testing
- Subcutaneous TXA injection before reconstruction, Subcutaneous TXA injection after reconstruction
- Volunteers
- 500 people, healthy volunteers welcome
- Sponsor
- The Cooper Health System
Brachial Plexus Block
Supraclavicular Brachial Plexus Block During Upper Limb Surgeries
Comparative Study Between Ketamine-Bupivacaine Versus Bupivacaine With Intravenous Ketamine Infusion In Supraclavicular Brachial Plexus Block During Upper limb Surgeries The techniques of regional anesthesia have become very…
- Trial name
- NCT05315271
- Testing
- Bupivacaine-ketamine injection, Bupivacaine injection with intravenous ketamine infusion
- Where
- Egypt
- Volunteers
- 60 people, healthy volunteers welcome
- Sponsor
- Sohag University
Ovarian Cancer, mRNA Vaccine
A Single-Arm, Open-Label, Prospective Study Evaluating the Safety, Tolerability, and Immunogenicity of the NeoOVSV Vaccine in Patients With Ovarian Cancer After Surgery
This is a Phase I, single-arm, open-label, prospective, non-randomized, single-center dose-escalation study. The study will evaluate the safety, tolerability, and preliminary activity of the NeoOVSV mRNA-lipid nanoparticle…
- Trial name
- NeoOVSV (NCT07724106)
- Testing
- Low Dose, middle dose, high dose
- Where
- China
- Volunteers
- 9 people
- Sponsor
- West China Hospital
Full-thickness Rotator Cuff Tear
InSpace™ System in Comparison to Best Repair of Massive Rotator Cuff Tear.
This is a post-marketing study to further assess the safety and effectiveness of the InSpace™ device implantation in comparison to surgical repair of full thickness Massive Rotator Cuff Tear .
- Trial name
- NCT02208440
- Testing
- Best Repair of torn Rotator Cuff, InSpace™ system
- Where
- United Kingdom
- Volunteers
- 14 people
- Sponsor
- OrthoSpace Ltd.
Spinal Fusion, Spinal Deformity
Pedicle Screw Malposition in Spine Arthrodesis Surgeries With O-ARM-guided Navigation
Background: Throughout the history of spinal deformity there have been continuous advances in the surgical treatment. Although many techniques have been successfully developed despite the anatomy complex, screw placement still…
- Conditions
- Spinal Fusion, Spinal Deformity, Spine Injury
- Trial name
- NoHARM (NCT06020417)
- Testing
- O-ARM (Medtronic, Inc, Louisville, CO), Conventional corrective surgery for arthrodesis
- Where
- Brazil
- Volunteers
- 124 people
- Sponsor
- Federal University of Piaui
Lung Tumor, Thoracoscopic Surgery
Mobile 3D C-arm CT for Lung Tumor Localization Efficacy Analysis: a Prospective Clinical Trial
It is well known that video-assisted thoracoscopic surgery (VATS) is preferred to open surgery for lung resection because of the smaller incisions and optimized postoperative recovery, including a shorter length of…
- Trial name
- NCT04974632
- Testing
- localization
- Where
- Taiwan
- Volunteers
- 41 people
- Sponsor
- Chang Gung Memorial Hospital