AzTrials
AzTrials

ArthrodesisNCT03257540

Early Weight-Bearing After Lapidus Arthrodesis

An observational study of Arthrodesis and Bunion, run by Paragon 28 at 3 sites in United States.

Terminated

Stopped early. The study ended before it was planned to and will not resume.

Official record
Search all trials

Trial summary

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… Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Arthrodesis, Bunion, Hallux Valgus
What is being tested?
Small Bone Intramedullary Nail
Type of treatment
Medical device
How many people
8 participants
Where
3 sitesUnited States
Study dates
31 Oct 2017to 31 Aug 2018
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

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.

Who may be able to join

  • 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.

Who cannot join

  • 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.
Show all 19Show fewer
  • 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.

Trial locations and contacts

3 sites in 1 country.

United States3 sites
  • Orthopedic Center of Palm Beach County

    Atlantis, Florida, 33462

  • Orthopaedic & Spine Center of the Rockies

    Fort Collins, Colorado, 80525

  • Redwood Orthopaedic Surgery Associates

    Santa Rosa, California, 95403

Other trials in United States

About this study

Official title: 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.

Read the 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.
Being tested
Small Bone Intramedullary Nail
Keywords
bunion, early weight-bearing, Lapidus, arthrodesis, intramedullary nail, Hallux Valgus
Medical subject headings
Ankylosis, Bunion, Hallux Valgus

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Small Bone Intramedullary NailDevice

    Also called Phantom Small Bone Intramedullary Nail - Lapidus

    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.

Study groups in NCT03257540
Study groupRoleWhat they receive
Small Bone Intramedullary NailAll study participants
Receives: Device: Small Bone Intramedullary Nail

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. 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.

    Measured: 6 months

Secondary outcomes (11)
  1. Clinical complications

    Complications due to the procedure or post-operative protocol or health conditions that could affect other outcome measures

    Measured: 24 Months

  2. Time to full weight-bearing

    The amount of time needed for a participant to become fully weight-bearing after the Lapidus surgery.

    Measured: 0 to 12 months

  3. 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

    Measured: Pre-operatively, 2 Weeks, 6 Weeks, 12 Weeks, 6 Months, 12 Months, 24 Months

  4. Change in VAS Pain Score across multiple time points

    Patient reported pain

    Measured: Pre-operatively, 2 Weeks, 6 Weeks, 12 Weeks, 6 Months, 12 Months, 24 Months

  5. Change in AOFAS Forefoot/Hallux Valgus Score across multiple time points

    Clinical score

    Measured: Pre-operatively, 2 Weeks, 6 Weeks, 12 Weeks, 6 Months, 12 Months, 24 Months

  6. Change in PROMIS Mobility Score across multiple time points

    Patient reported mobility assessment, Item Bank v2.0

    Measured: Pre-operatively, 2 Weeks, 6 Weeks, 12 Weeks, 6 Months, 12 Months, 24 Months

  7. Change in PROMIS Pain Interference Score across multiple time points

    Patient reported pain interference assessment, Item Bank v1.0, SF 6a

    Measured: Pre-operatively, 2 Weeks, 6 Weeks, 12 Weeks, 6 Months, 12 Months, 24 Months

  8. Change in PROMIS Pain Intensity Score across multiple time points

    Patient reported pain intensity assessment, Item Bank v1.0, SF 3a

    Measured: Pre-operatively, 2 Weeks, 6 Weeks, 12 Weeks, 6 Months, 12 Months, 24 Months

  9. Evaluate time to return to work post-operatively while noting labor classification

    sedentary, light labor, medium labor, heavy labor, very heavy labor

    Measured: 0 to 24 months

  10. Evaluate time to return to full duty work post-operatively while noting labor classification

    sedentary, light labor, medium labor, heavy labor, very heavy labor

    Measured: 0 to 24 months

  11. Change in Range of Motion across multiple time points

    1st MTP Dorsiflexion

    1st MTP Plantarflexion Ankle Dorsiflexion Ankle Plantarflexion

    Measured: Pre-operatively, 2 Weeks, 6 Weeks, 12 Weeks, 6 Months, 12 Months, 24 Months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 Aug 2017
  2. Study start31 Oct 2017
  3. Primary completion31 Aug 2018
  4. Study completion31 Aug 2018

Why it stopped: Low enrollment

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case only
Time perspective
Prospective
Enrolment
8 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03257540
Sponsor's protocol ID
P30-SP-0001
Status last verified
Oct 2018
First submitted
18 Aug 2017
Last updated
17 Oct 2018
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
Yes
Individual data sharing
No

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.

    PubMed 22292592

Questions about this trial

What is this clinical trial studying?

An observational study of Arthrodesis and Bunion, run by Paragon 28 at 3 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 19 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: stopped early, as of the sponsor's last update on 17 Oct 2018. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 3 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study was stopped early (reason given: Low enrollment). Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Clinical/radiographic healing (time frame: 6 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT03257540, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 Oct 2018.

Free account

Keep searching with a free account

You’ve used your 3 free searches for this session. Log in or create a free AzTrials account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in