Clinical trials: Hallux Valgus (Bunions)
Hallux Valgus and Bunion
Epidemiology of Bunion and Risk Factors
Analysis of the collected data to determine: Prevalence. Risk factors. Radiological and clinical patterns and their association with specific risk factors Of Hallux Valgus
- Trial name
- NCT06335459
- Testing
- epidemiology
- Volunteers
- 2,000 people, healthy volunteers welcome
- Sponsor
- Assiut University
Hallux Valgus, Bunion
Clinical Trial on Patient-Specific-Instrumentation Assisted Lapidus Fusion for Hallux Valgus
RCT to compare the effectiveness of PSI assisted Lapidus surgery vs conventional Lapidus surgery in hallux valgus.
- Conditions
- Hallux Valgus, Bunion, Patient Spe
- Trial name
- NCT05602844
- Testing
- PSI Lapidus, Conventional Lapidus
- Where
- Hong Kong
- Volunteers
- 54 people
- Sponsor
- Chinese University of Hong Kong
Hallux Valgus and Bunion (Disorder)
FASTFORWARDTM Bunion Correction System in Treating Hallux Valgus Patients
The FASTFORWARDTM Bunion Correction system has been cleared by the United States Food and Drug Administration for sale. This study is to investigate the clinical outcome of MedShape FASTFORWARDTM Bunion Correction system in…
- Trial name
- NCT03594292
- Testing
- FASTFORWARDTM Bunion, Conventional surgery
- Where
- Taiwan
- Volunteers
- 12 people
- Sponsor
- China Medical University Hospital
Hallux Valgus (Bunions)
Liposome Bupivacaine for ANKLE Blocks
Postoperative analgesia for hallux valgus surgery (bunionectomy) is inconsistent and may even result in rebound pain when the (ankle) blocks wear off.
- Trial name
- NCT03106545
- Testing
- Liposome bupivacaine
- Where
- Belgium
- Volunteers
- 40 people
- Sponsor
- Catherine Vandepitte, M.D.
Hallux Valgus
Patient Reported Function Following Combined First MTP and First TMT Arthrodesis.
The goal of the study is to gather sufficient patient data to assess real world postoperative function after a first metatarsophalangeal (MTP) joint arthrodesis done in conjunction with first tarsometatarsal arthrodesis (TMT)…
- Trial name
- NCT05527197
- Testing
- Lapiplasty
- Where
- United States
- Volunteers
- 31 people, healthy volunteers welcome
- Sponsor
- Midwest Bunion Center, LLC
Arthralgia, Bunion
A Study to Evaluate the Effectiveness and Safety of Tapentadol(CG5503) in the Treatment of Acute Pain From Bunionectomy Compared With Placebo Followed by a Voluntary Open Label Extension for Safety.
The purpose of this study is to evaluate the effectiveness (level of pain control) and safety of the administration of 3 different dose levels of CG5503 compared with oxycodone and with placebo in patients who have had a…
- Conditions
- Arthralgia, Bunion, Hallux Valgus, Pain Assessment
- Trial name
- NCT00364247
- Testing
- CG5503 IR;tapentadol
- Volunteers
- 602 people
- Sponsor
- Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
Arthralgia, Bunion
A Study to Evaluate the Effectiveness and Safety of Tapentadol (CG5503) in the Treatment of Acute Pain From Bunionectomy.
The purpose of this study is to evaluate the effectiveness (level of pain control) and safety of the administration of 2 different dose levels of tapentadol (CG5503) compared with oxycodone and with placebo in subjects who have…
- Conditions
- Arthralgia, Bunion, Hallux Valgus, Pain
- Trial name
- NCT00613938
- Testing
- Tapentadol (CG5503), oxycodone
- Where
- 7 sites in United States
- Volunteers
- 901 people
- Sponsor
- Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
Hallux Valgus and Bunion
Post-Operative Pain and Opioid Reduction Trial After Bunionectomy
This is a Phase 2b, randomized, double blind, placebo and active controlled study with an Ascending Dose Stage and an optional Dose Expansion Stage in subjects undergoing bunionectomy.
- Trial name
- MERIT-2 (NCT05411861)
- Testing
- Analgesic Non Narcotic
- Where
- 3 sites in United States
- Volunteers
- 73 people
- Sponsor
- Cali Pharmaceuticals LLC
Rotator Cuff Repair, Ankle Arthroplasty or Arthrodesis
Ultrasound-Guided Percutaneous Peripheral Nerve Stimulation: A Department of Defense Funded Pragmatic Clinical Trial
Postoperative pain is usually treated with opioids that have undesirable and sometimes dangerous side effects (e.g., vomiting and respiratory depression)-and yet over 80% of patients still experience inadequate pain relief.
- Conditions
- Rotator Cuff Repair, Ankle Arthroplasty or Arthrodesis, Hallux Valgus (Bunion) Resection
- Trial name
- NCT04713098
- Testing
- Peripheral Nerve Stimulation
- Where
- 6 sites in United States
- Volunteers
- 250 people
- Sponsor
- University of California, San Diego
Hallux Valgus, Hallux Valgus and Bunion
Arthroscopic Assisted Lateral Soft Tissue Release for Hallux Valgus
Lateral soft tissue release is commonly performed as part of the surgical correction of hallux valgus. This study will look at the results form a series of patients whom have underwent the arthroscopic lateral soft tissue release.
- Trial name
- NCT04088214
- Testing
- Arthroscopic lateral soft tissue release
- Where
- Hong Kong
- Volunteers
- 12 people
- Sponsor
- Chinese University of Hong Kong
Bunion, Hallux Rigidus
Pericapsular Exparel for Pain Relief in Bunionectomy and Related Procedures
Exparel is an FDA-approved local anesthetic (bupivacaine), in a long-release formulation. In this study the investigators plan to determine the ability of Exparel to control post-operative pain in common first metatarsophalangeal…
- Trial name
- NCT02499575
- Testing
- 0.5% ropivacaine, Exparel
- Where
- 2 sites in United States
- Volunteers
- 2 people
- Sponsor
- OhioHealth
Bunion
LSTR in Chevron Osteotomy
The goal of this clinical trial is to determine if performing a lateral soft tissue release during a Chevron osteotomy (or Akin osteotomy when appropriate) for bunions leads to better correction without added complications in 200…
- Trial name
- NCT06486753
- Testing
- Chevron osteotomy bunion surgery with lateral soft tissue release
- Where
- United States
- Volunteers
- 200 people
- Sponsor
- The Methodist Hospital Research Institute
Hallux Valgus Deformity, Hallux Valgus (Bunion) Resection
Fourth Generation Percutaneous Transverse Osteotomies for Hallux Valgus
The goal of this observational study is to learn if percutaneous transverse osteotomies for hallux valgus deformity are safe and effective. The main questions it aims to answer are: 1.
- Conditions
- Hallux Valgus Deformity, Hallux Valgus (Bunion) Resection, Hallux Valgus Surgery, Hallux Deformity
- Trial name
- NCT06625229
- Where
- Australia
- Volunteers
- 483 people
- Sponsor
- Orthopaedic and Arthritis Specialist Centre
Hallux Valgus and Bunion, Sedation
Dexmedetomidine Sedation in Orthopedic Surgery
60 patients ASA I-III, undergoing orthopedic surgery will be randomly assigned into one of three groups, namely group A (n=20), where dexmedetomidine will be used for sedation (initial bolus dose followed by continuous infusion)…
- Trial name
- NCT04149626
- Testing
- Dexmedetomidine, Midazolam, Remifentanil
- Where
- Greece
- Volunteers
- 60 people
- Sponsor
- Asklepieion Voulas General Hospital