Clinical Trials Logo

Hallux Limitus clinical trials

View clinical trials related to Hallux Limitus.

Filter by:

NCT ID: NCT02350881 Completed - Clinical trials for Rheumatoid Arthritis

A Post-Marketing Observational Study to Evaluate Primus™ FGT Implant at a Minimum of 5 Years Follow-up

Start date: May 2013
Phase: N/A
Study type: Observational

Foot silicone implants suffer from bad reputation on the market, due to poor results obtained with the first generations of implants. Allergies to silicone, infections due to silicone and implants breakage used to be common with previous generations of silicone implants. Publications relative to those implants showed that the survival rates after 5 years of follow-up were unsatisfactory. Since 1998, Tornier has been selling a new generation of silicone implants made of Ultrasil™. The use of this new material in its manufacturing process together with its innovative geometry, make the Primus™ FGT a much more resistant, anatomic and long lasting implant. The main objective of this study is to evaluate the clinical outcomes of the implantation of Primus™ FGT implant in great toe arthroplasty. The study will capture long term outcomes in terms of functional metrics from documented clinical data. Other objectives are to evaluate the outcomes in terms of radiological evaluation and of safety during all the follow-up.

NCT ID: NCT01825356 Completed - Hallux Rigidus Clinical Trials

Amniotic Membrane as an Adjunct Treatment for Hallux Rigidus

Start date: April 8, 2013
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether patients undergoing a dorsal cheilectomy procedure with implementation of amniotic membrane tissue results in improved clinical and functional outcomes compared to a standard dorsal cheilectomy procedure. Specific Aim 1: To compare American Orthopedic Foot and Ankle Society (AOFAS) scores between patients undergoing dorsal cheilectomy to patients undergoing dorsal cheilectomy with implantation of amniotic membrane tissue. Hypothesis 1: Clinical and functional outcomes, as measured by the AOFAS , in the patients undergoing dorsal cheilectomy with implantation of amniotic membrane tissue will be superior to those without. Specific Aim 2: To compare range of motion between patients undergoing dorsal cheilectomy to patients undergoing dorsal cheilectomy with implantation of amniotic membrane tissue. Hypothesis 2: Patient to undergo dorsal cheilectomy and implantation of amniotic membrane tissue will demonstrate less postoperative stiffness as measured from the pre-and postoperative radiographs. Specific Aim 3: To compare Foot Function Index (FFI) scores between patients undergoing dorsal cheilectomy to patients undergoing dorsal cheilectomy with implantation of amniotic membrane tissue. Hypothesis 3: Clinical and functional outcomes, as measured by the FFI, the patients undergoing dorsal cheilectomy with implantation of amniotic membrane tissue will be superior to those without.

NCT ID: NCT01804491 Completed - Hallux Rigidus Clinical Trials

Motion Analysis in Patients With Hallux Rigidus

Start date: October 2006
Phase: N/A
Study type: Observational

The aim was to investigate with a multi-segmental foot model the kinetic and kinematic in patients with a hallux rigidus, before and after different type of surgery.

NCT ID: NCT01589679 Terminated - Hallux Limitus Clinical Trials

Contracture Reduction Following Bunionectomy: a Longitudinal, Controlled Trial

Bunionectomy
Start date: April 2012
Phase: N/A
Study type: Interventional

To determine the efficacy of Metatarsal Dynasplint Sytem (MTP) in reducing contracture of hallux limitus secondary to Bunionectomy, in a longitudinal, controlled trial.

NCT ID: NCT01284985 Completed - Osteoarthritis Clinical Trials

Short Term Follow-up of Patient Implanted With the Metatarso-Phalangeal Prosthesis METIS®

Start date: February 2009
Phase: N/A
Study type: Observational

The great toe is vital for normal, pain free ambulation. Decreased function associated with osteoarthritis of the first matatarsal phalangeal joint (MTP I) often called Hallux Rigidis or Hallux Limitus leading to a painful great toe. Patients experience pain during ambulation especially during the push-off phase of gait. When surgery is indicated four techniques are used for hallux rigidis; cheilectomie, resection arthroplasty, arthrodesis and implant surgery (1). Endoprostetic implants are relatively new. Silicone Implants like the arthroplasty developed by Swanson (2) resulted in foreign body reactions and periarticular bone loss. Subsequent implants, in particular the metallic hemi arthroplasty with or without polyethylene articulations, have been more successful (3). Still, implants are prone to wear of the material and show higher rates of loosening and infection compared to other techniques (4;5). In the last decades several new implants are described using two non cemented pressfit components, of titanium alloy or ceramic (6-9). Between 2001 and 2004 the investigators developed a new concept with instrumentation for exact alignment to prevent for wear with loosening of the implant on the long term. The implant has bone-conserving characteristics to enable arthrodesis as a salvage procedure. It is a completely modular two-component press fit titanium alloy implant with polyethylene insert that can be used as either for hemi-, total- or revision arthroplasty. The purpose of this study is to have an overview of clinical status of the patient implanted with the METIS® prosthesis at short term (2 years of follow-up). The objective of this study is to evaluate the safety and efficacy of the Metatarso-Phalangeal prosthesis METIS® at short term follow up.

NCT ID: NCT01048450 Completed - Hallux Rigidus Clinical Trials

Surgical Treatment for Hallux Rigidus

Start date: July 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to examine the long-term outcomes for the surgical treatment of end stage degeneration in the big toe joint.

NCT ID: NCT01028469 Recruiting - Osteoarthritis Clinical Trials

Artelon Metatarsophalangeal (MTP) Spacer

Start date: December 2009
Phase: Phase 4
Study type: Interventional

The aim of this prospective, case series is to evaluate the surgical treatment of painful and disabling osteoarthrosis in the MTP-I joint by insertion of an Artelon MTP Spacer.

NCT ID: NCT00717691 Completed - Hallux Limitus Clinical Trials

Hallux Limitus Treated With Dynamic Splinting: A Randomized, Controlled Trial

Start date: July 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to regain range of motion of the great toe with dynamic splinting which will help reduce great toe's pain and swelling.

NCT ID: NCT00285116 Withdrawn - Hallux Rigidus Clinical Trials

The Correlation Between Fasicitis Plantaris and Hallux Rigidus

Start date: n/a
Phase: N/A
Study type: Interventional

Comparison between 3 groups: - group I has hallux rigidus. Is fasicitis plantaris present? - group II has fasicitis plantaris. Does the hallux have limited mobility? - group III does not have hallux rigidus or fasicitis plantaris

NCT ID: NCT00284362 Withdrawn - Hallux Rigidus Clinical Trials

Prospective and Comparative Analysis of Arthroscopic and Open Surgery for Hallux Rigidus

Start date: n/a
Phase: N/A
Study type: Interventional

Comparison between arthroscopic and open surgery for hallux rigidus.