Early Weight-Bearing After Lapidus Arthrodesis

Prospective Clinical Evaluation of Early Weight-Bearing After Lapidus Arthrodesis Using the Phantom™ Intramedullary Nail

The goal of this research study is to determine if union rates are affected by early weight-bearing after Lapidus Arthrodesis using the Phantom™ Intramedullary Nail.

The study hypothesis is that the union rate for those who undergo a Lapidus Arthrodesis procedure with the Phantom™ Intramedullary Nail and participate in an early weight-bearing protocol will be non-inferior to union rates previously published for this procedure.

Study Overview

• Status: Terminated
• Conditions: Bunion; Hallux Valgus; Arthrodesis
• Intervention / Treatment: Device: Small Bone Intramedullary Nail

Detailed Description

Each subject will undergo a Lapidus Arthrodesis which entails cartilage removal from the 1st TMT joint, subchondral bone preparation, deformity correction, temporary fixation and permanent fixation with the Phantom™ Intramedullary Nail. The Phantom™ Intramedullary Nail is inserted by drilling a hole for the nail at a specified location using instrumentation and a targeting guide. The nail is inserted into the drill hole and is fixated to the medial cuneiform and 1st metatarsal using three threaded pegs and a locking screw.

A subchondral drill and chisel are provided in the system with the Lapidus Nail. Subchondral drilling and feathering of the subchondral bone with a chisel are standard ways to prepare the subchondral bone and elicit bleeding bone prior to arthrodesis. Use of this instrumentation is encouraged for this study to ensure that proper bone preparation is performed for arthrodesis. A torque indicating driver is also encouraged to be used for this procedure to help guide the surgeon to appropriate compression to apply across the joint. Alternatively, a standard driver and handle can be used with two-finger tightness when compressing the joint to achieve a similar effect.

Traditionally, it is common for people who undergo a Lapidus Arthrodesis to be non-weight-bearing for 6-8 Weeks following the surgical procedure. This time allows the bones to properly fuse together. During this 6-8 week period, people can be limited in the typical day-to-day activities they participate in, such as walking, shopping and working.

The Phantom™ Intramedullary Nail may allow subjects to bear weight earlier than traditional procedures without negatively effecting fusion. By allowing people to bear weight earlier than traditional methods, it is possible that people will have the opportunity to resume typical day-to-day activities faster than usual.

The study in question will investigate the Phantom™ Intramedullary Nail with the following early weight-bearing protocol (see "Post-Operative Protocol for Study Participant" below).

The study preference is that subjects are placed in a splint from 0-2 Weeks. However, a cast may be substituted according to surgeon preference. No casts are permitted beyond 2 Weeks, unless deemed as a medical necessity in which case the subject would no longer follow the early weight-bearing protocol.

The study preference is that subject will be placed in a walking boot at 2 Weeks. However, an immobilizing shoe may be substituted according to surgeon preference.

Post-Operative Protocol for Study Participant

Activity Level Definitions:

Sedentary: Most activities are done seated or lying down. Surgically repaired foot should be raised when in seated or reclined position. Standing limited to less than 15 minutes per hour. Moving is limited to necessary activities such as going to the bathroom or food preparation.

Light Activity: Standing limited to less than 30 minutes per hour. Movement is mostly limited to in-home movement such as folding laundry or wiping counters. Short time periods of movement to leave the house can be performed for necessary activities (such as the grocery store), but should be limited to less than 30 minutes of standing time.

Moderate Activity: No limits on standing. Walking limited to 45 minute time periods no more than 3 times per day. No running, jumping or heavy lifting (more than 25 pounds).

Heavy Activity: No limits on walking, running and jumping. No lifting limits.

0-2 Weeks After Surgery:

• Footwear: You will have a splint (or cast) on your surgically repaired foot/leg. The splint (or cast) should not be removed. You will wear a comfortable shoe on the other foot.
• Weight-Bearing: Do not put any weight on your surgically repaired foot.
• Mobility Aid: You will use a walking aid such as crutches, rolling knee scooter or wheelchair to keep all weight off of your surgically repaired foot.
• Range of Motion Exercises: None.
• Activity level: Sedentary after surgery working up to light activity over two Weeks (restarting activities of daily living without putting weight on your foot).

2-6 Weeks After Surgery:

• Footwear: A restrictive boot (or shoe) will be given to you by your doctor. This should not be removed other than for range of motion exercises and bathing (seated). Wear a comfortable shoe on the other foot.
• Weight-Bearing: Put weight on your foot as you can tolerate in the restrictive boot (or shoe). Do not walk without the restrictive boot (or shoe).
• Mobility Aid: If possible, no walking aid should be used. If needed for pain, use a walking aid as necessary.
• Range of Motion Exercises: You will do range of motion exercises without the restrictive boot (or shoe) with no weight on your foot, as instructed by your doctor.
• Activity level: Light activity with restrictive boot (or shoe). 6 Weeks-3 Months After Surgery:
• Footwear: You will wear a restrictive boot (or shoe) working up to supportive shoe (preferably a lace-up or Velcro shoe including sneakers, running shoes, work boots or soft leather shoes without a heel) by 8 Weeks after your surgery.
• Weight-Bearing: Put weight on your foot as you can tolerate. Barefoot walking is not encouraged.
• Mobility Aid: No help from crutches, scooter, or wheelchair.
• Range of Motion Exercises: You will do range of motion exercises as instructed by your doctor.
• Activity level: Light activity working up to moderate activity (low impact) as you can tolerate.

3-6 Months After Surgery:

• Footwear: At Month 3-4, move from a supportive shoe to footwear of your choice, as you can tolerate.
• Weight-Bearing: Put weight on your foot as you can tolerate.
• Mobility Aid: No help from crutches, scooter, or wheelchair.

• Activity level: Moderate activity for 3-4 Months post-operative, slowly moving into heavy activity as you can tolerate after Month 4.

  6 Months - 2 Years After Surgery:

• Footwear: You have no restrictions on footwear.
• Weight-Bearing: Put weight on your foot as you can tolerate.
• Mobility Aid: No help from crutches, scooter, or wheelchair.
• Activity Level: No activity limits.

• Study Type: Observational
• Enrollment (Actual): 8

Contacts and Locations

Study Locations

• United States
  • California
    • Santa Rosa, California, United States, 95403
      • Redwood Orthopaedic Surgery Associates
  • Colorado
    • Fort Collins, Colorado, United States, 80525
      • Orthopaedic & Spine Center of the Rockies
  • Florida
    • Atlantis, Florida, United States, 33462
      • Orthopedic Center of Palm Beach County

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

• Sampling Method: Non-Probability Sample

Study Population

The study population will consist of adults age 18 and older with a painful bunion deformity. The most common age demographic to have surgery for hallux valgus correction is age 50-59. Additionally, the prevalence of hallux valgus in females is greater than males, so a higher percentage of female subjects seeking treatment is likely to be expected.

This population is suitable for the purpose of the investigation, as groups most likely to seek treatment (surgical) for hallux valgus correction will be represented in this study.

Description

Inclusion Criteria:

• The subject is at least 18 years of age with closed physeal plates at the time of screening.
• The intermetatarsal angle is greater than or equal to 10 degrees.
• The hallux valgus angle is greater than or equal to 25 degrees.
• The subject has foot pain/discomfort on the foot in question.
• The subject has activity limitations due to the foot in question.
• The subject agrees to comply with the requirements of the study and complete the study measures.
• The subject is willing and able to provide written informed consent.

Exclusion Criteria:

• The subject is pregnant.
• The subject is a current smoker.
• The subject has been clinically diagnosed with diabetes.
• The subject has been clinically diagnosed with peripheral neuropathy.
• The subject had been previously sensitized to titanium.
• The subject currently takes oral steroids or rheumatoid biologics.
• The subject has had previous surgery for hallux valgus on operative side.
• The subject has insufficient quantity or quality of bone to permit stabilization, conditions that retard healing (not including pathological fractures) and conditions causing poor blood supply such as peripheral vascular disease.
• The subject has a history of delayed or non-union for fracture or joint.
• The subject has an active, suspected or latent infection in the affected area.
• The subject will require a structural graft in the 1st TMT joint.
• The subject is scheduled to undergo a concomitant 2nd tarsometatarsal joint arthrodesis procedure.
• The subject is scheduled to undergo a same-day bilateral procedure.
• The subject cannot be scheduled for surgery within 3 months of the pre-operative exam.
• The subject has previously been enrolled into this study for a contralateral procedure.
• The subject is actively involved with a Workman's Compensation case.
• The subject is not expected to complete the study according to the investigation plan.
• The subject has been deemed physiologically or psychologically inadequate by the enrolling physician.
• The subject is: a prisoner, unable to understand what participation in the study entails, mentally incompetent, a known abuser of alcohol and/or drugs or anticipated to be non-compliant.

Study Plan

How is the study designed?

Design Details

• Observational Models: Case-Only
• Time Perspectives: Prospective

Number of groups / cohorts

1

Cohorts and Interventions

Group / Cohort	Intervention / Treatment
Small Bone Intramedullary Nail; All study participants	Device: Small Bone Intramedullary Nail; Patients undergoing a Lapidus Arthrodesis procedure for hallux valgus correction who are receiving a Phantom Small Bone Intramedullary nail will begin weight-bearing at 2 weeks and follow a pre-determined post-operative protocol.; Other Names: Phantom Small Bone Intramedullary Nail - Lapidus

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Clinical/radiographic healing	Evaluate clinical/radiographic healing (union vs. non-union) after a Lapidus arthrodesis procedure at 6 months following a surgery using the Phantom Intramedullary nail with early weightbearing at 2 weeks.	6 months

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Clinical complications	Complications due to the procedure or post-operative protocol or health conditions that could affect other outcome measures	24 Months
Time to full weight-bearing	The amount of time needed for a participant to become fully weight-bearing after the Lapidus surgery.	0 to 12 months
Change in radiographic angular/positional alignment before and after the Lapidus procedure	Hallux Abductus Angle Intermetatarsal Angle First Metatarsal Declination Angle Distal Metatarsal Articular Angle Sesamoid Position	Pre-operatively, 2 Weeks, 6 Weeks, 12 Weeks, 6 Months, 12 Months, 24 Months
Change in VAS Pain Score across multiple time points	Patient reported pain	Pre-operatively, 2 Weeks, 6 Weeks, 12 Weeks, 6 Months, 12 Months, 24 Months
Change in AOFAS Forefoot/Hallux Valgus Score across multiple time points	Clinical score	Pre-operatively, 2 Weeks, 6 Weeks, 12 Weeks, 6 Months, 12 Months, 24 Months
Change in PROMIS Mobility Score across multiple time points	Patient reported mobility assessment, Item Bank v2.0	Pre-operatively, 2 Weeks, 6 Weeks, 12 Weeks, 6 Months, 12 Months, 24 Months
Change in PROMIS Pain Interference Score across multiple time points	Patient reported pain interference assessment, Item Bank v1.0, SF 6a	Pre-operatively, 2 Weeks, 6 Weeks, 12 Weeks, 6 Months, 12 Months, 24 Months
Change in PROMIS Pain Intensity Score across multiple time points	Patient reported pain intensity assessment, Item Bank v1.0, SF 3a	Pre-operatively, 2 Weeks, 6 Weeks, 12 Weeks, 6 Months, 12 Months, 24 Months
Evaluate time to return to work post-operatively while noting labor classification	sedentary, light labor, medium labor, heavy labor, very heavy labor	0 to 24 months
Evaluate time to return to full duty work post-operatively while noting labor classification	sedentary, light labor, medium labor, heavy labor, very heavy labor	0 to 24 months
Change in Range of Motion across multiple time points	1st MTP Dorsiflexion 1st MTP Plantarflexion Ankle Dorsiflexion Ankle Plantarflexion	Pre-operatively, 2 Weeks, 6 Weeks, 12 Weeks, 6 Months, 12 Months, 24 Months

Collaborators and Investigators

• Sponsor: Paragon 28

Publications and helpful links

General Publications

• Casaburi R, Porszasz J, Hecht A, Tiep B, Albert RK, Anthonisen NR, Bailey WC, Connett JE, Cooper JA Jr, Criner GJ, Curtis J, Dransfield M, Lazarus SC, Make B, Martinez FJ, McEvoy C, Niewoehner DE, Reilly JJ, Scanlon P, Scharf SM, Sciurba FC, Woodruff P; COPD Clinical Research Network. Influence of lightweight ambulatory oxygen on oxygen use and activity patterns of COPD patients receiving long-term oxygen therapy. COPD. 2012 Feb;9(1):3-11. doi: 10.3109/15412555.2011.630048.

Study record dates

Study Major Dates

• Study Start (Actual): October 31, 2017
• Primary Completion (Actual): August 31, 2018
• Study Completion (Actual): August 31, 2018

Study Registration Dates

• First Submitted: August 18, 2017
• First Submitted That Met QC Criteria: August 18, 2017
• First Posted (Actual): August 22, 2017

Study Record Updates

• Last Update Posted (Actual): October 17, 2018
• Last Update Submitted That Met QC Criteria: October 15, 2018
• Last Verified: October 1, 2018

More Information

Terms related to this study

• Keywords: arthrodesis; bunion; Hallux Valgus; intramedullary nail; early weight-bearing; Lapidus
• Additional Relevant MeSH Terms: Musculoskeletal Diseases; Foot Deformities; Foot Deformities, Acquired; Hallux Valgus; Bunion
• Other Study ID Numbers: P30-SP-0001

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: No

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: Yes
• product manufactured in and exported from the U.S.: No