ArthrodesisNCT03257540
Early Weight-Bearing After Lapidus Arthrodesis
An observational study of Arthrodesis and Bunion, run by Paragon 28 at 3 sites in United States.
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
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.
- Conditions
- Arthrodesis, Bunion, Hallux Valgus
- 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 group | Role | What they receive |
|---|---|---|
| Small Bone Intramedullary Nail | All 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.
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)
Clinical complications
Complications due to the procedure or post-operative protocol or health conditions that could affect other outcome measures
Measured: 24 Months
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
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
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
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
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
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
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
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
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
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.
- First posted22 Aug 2017
- Study start31 Oct 2017
- Primary completion31 Aug 2018
- Study completion31 Aug 2018
Why it stopped: Low enrollment
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for ArthrodesisStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Paragon 28
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
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
Study at a glance
From the registry record, last updated by the sponsor on 17 Oct 2018. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Prospective Clinical Evaluation of Early Weight-Bearing After Lapidus Arthrodesis Using the Phantom™ Intramedullary Nail
- ClinicalTrials.gov ID
- NCT03257540
- Acronym / sponsor ID
- P30-SP-0001
- Conditions
- Arthrodesis, Bunion, Hallux Valgus
- Keywords
- bunion, early weight-bearing, Lapidus, arthrodesis, intramedullary nail, Hallux Valgus
- Study type
- Observational
- Recruitment status
- TerminatedReason stopped: Low enrollment
- Enrolment
- 8 participants (actual)
- Lead sponsor
- Paragon 28Industry (pharma, biotech, devices)
- Study start
- 31 Oct 2017 (actual)
- Primary completion
- 31 Aug 2018 (actual)
- Study completion
- 31 Aug 2018 (actual)
- First posted
- 22 Aug 2017 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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 design
- Observational model
- Case only
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Small Bone Intramedullary Nail | – | Device: Small Bone Intramedullary NailAll study participants |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- 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.
Key inclusion criteria (7 listed)
- 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.
Key exclusion criteria (19 listed)
- 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.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Small Bone Intramedullary NailAlso: Phantom Small Bone Intramedullary Nail - LapidusPatients 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. | Device | Small Bone Intramedullary Nail |
Primary outcome
Clinical/radiographic healing
Time frame: 6 months
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.
11 secondary outcomes
Clinical complications
Time frame: 24 Months
Time to full weight-bearing
Time frame: 0 to 12 months
Change in radiographic angular/positional alignment before and after the Lapidus procedure
Time frame: Pre-operatively, 2 Weeks, 6 Weeks, 12 Weeks, 6 Months, 12 Months, 24 Months
Change in VAS Pain Score across multiple time points
Time frame: 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
Time frame: Pre-operatively, 2 Weeks, 6 Weeks, 12 Weeks, 6 Months, 12 Months, 24 Months
Change in PROMIS Mobility Score across multiple time points
Time frame: Pre-operatively, 2 Weeks, 6 Weeks, 12 Weeks, 6 Months, 12 Months, 24 Months
Change in PROMIS Pain Interference Score across multiple time points
Time frame: Pre-operatively, 2 Weeks, 6 Weeks, 12 Weeks, 6 Months, 12 Months, 24 Months
Change in PROMIS Pain Intensity Score across multiple time points
Time frame: 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
Time frame: 0 to 24 months
Evaluate time to return to full duty work post-operatively while noting labor classification
Time frame: 0 to 24 months
Change in Range of Motion across multiple time points
Time frame: Pre-operatively, 2 Weeks, 6 Weeks, 12 Weeks, 6 Months, 12 Months, 24 Months
Results and safety
The study was stopped early (reason given: Low enrollment). Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 17 Oct 2018.
- Derived from this study: PubMed 22292592Casaburi 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.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
3 sites in 1 country: see every site and its status.
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.