Diabetic WoundPhase 4NCT04405765
Cryopreserved vs. Lyopreserved Stravix as an Adjunct to NPWT in the Treatment of Complex Wounds
A Phase 4 study testing NPWT and lyopreserved Stravix and NPWT and cryopreserved Stravix in people with Diabetic Wound, run by University of Texas Southwestern Medical Center at 1 site in United States.
Trial summary
This study is a prospective, 2-arm parallel assignment, randomized clinical trial to compare lyopreserved vs cryopreserved Stravix as an adjunct therapy to NPWT. Read more about this study
- Who is it for?
- Ages 21 years and older
- Conditions the study is for
- Diabetic Wound
- What is being tested?
- NPWT and lyopreserved Stravix and NPWT and cryopreserved Stravix
- Type of treatment
- Medical device
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 46 participants
- Where
- 1 siteUnited States
- Study dates
- 22 Jun 2021to 7 Jul 2022
- Phase
- Phase 4
- Are there results?
- Yes, posted in the registrySummary in the doctors' view
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 21 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Diagnosis of a diabetes mellitus
- Men/women ≥21 years old
- Post-operative foot or ankle wounds sized >4cm2 that have presented for <1 year
- ABI ≥0.5 or toe pressures >30 mmHg
- Wounds indicated for treatment with NPWT
Who cannot join
- Active Charcot arthropy
- Unable to use NPWT at home
- Untreated bone or soft tissue infection
- Is pregnant or plans to become pregnant
- Is nursing or actively lactating
- Developmental disability/significant psychological disorder that in the opinion of the investigator could impair the subject's ability to provide informed consent, participate in the study protocol or record study measures, including untreated schizophrenia, bipolar disorder and psychiatric hospitalization within the last 2 years.
- Active alcohol or substance abuse in the opinion of the investigator that could impair the subject's ability to provide informed consent, participate in the study protocol or record study materials
Trial locations and contacts
1 site in 1 country.
United States1 site
UT Southwestern Medical Center at Dallas
Dallas, Texas, 75390
About this study
Official title: Prospective, Randomized, Single-Center Study to Compare Clinical Outcomes Between Cryopreserved and Lyopreserved Stravix as an Adjunct to NPWT in the Treatment of Complex Wounds
This study is a prospective, 2-arm parallel assignment, randomized clinical trial to compare lyopreserved vs cryopreserved Stravix as an adjunct therapy to NPWT.
Read the detailed description
Screening
- Explain purpose and nature of the study and obtain signature on the informed consent document.
- Screen the subject against protocol inclusion and exclusion criteria, including all pertinent tests, including pregnancy test 3. Complete SF-36, EuroQol 5 dimensions (EQ-5D) and PROMIS® Baseline (may be done as same day as screening procedures or within +2 days of screening and before start of Therapy/Treatment Phase)
- Obtain general medical history and demographic information and social history
- Complete a physical examination, body weight, height, and vital signs, including measurement of resting heart rate, respiratory rate, and blood pressure while seated.
- Select target study ulcer
- Obtain complete history pertinent to DFU disease including duration of the target ulcer, previous and current treatment. Document ulcer classification.
- Perform debridement and obtain tissue collection (3 tissue and 1 bone).
- Perform standardized photography and measurement of the study wound (eKare or available camera with ruler). Assess the post-debridement ulcer area (cm2), perimeter (cm), and greatest depth (cm) using the inSight device (eKare, Fairfax, VA). These values are the baseline measurements for calculating wound closure rate at the two-week run-in visit.
- Perform hyperspectral imaging of dorsal and plantar aspects of the foot.
- Perform neuropathy assessment
- Collect all relevant concomitant medication (antibiotics, antifungals and other anti-infective therapies)
- Place Stravix (lyo or cryo per randomization schedule) and dress wound for NPWT therapy.
- Document size of Stravix used.
- Disburse subject stipend Therapy/Treatment Phase (Weekly visits +/- 4 days)
Study Visit 1-11:
- Assess target ulcer (if wound has closed, document as such, skip to step 5).
- Document time on/off NPWT if applicable.
- Perform standardized photography of the study wound when NPWT is removed.
- If Stravix is removed, assess the ulcer area (cm2), perimeter (cm), and greatest depth (cm) using the inSight device - if the wound is deemed closed by the physician, skip to EOS visit.
- Perform hyperspectral imaging of the dorsal and plantar aspects of the foot if wound is active or closed.
- Debride wound if indicated. Re-measure wound if surgical debridement is performed prior to dressing the wound.
- Collect all relevant concomitant medication.
- If wound is still active, redress the wound with assigned Stravix (if removed for debridement) and NPWT. Document all dressings applied including size of Stravix.
- Disburse subject stipend
- Note: at week 4, if wound is not ready for grafting, remove existing Stravix and replace with new piece of Stravix (per randomization schedule)
- Assess for AE/SAEs and/or follow up on previous AE/SAEs.
Study Visit Closed 1. When a subject's study wound has closed, they will perform the EOS evaluation.
Study Visit 12/EOS:
- At the time of wound closure, subjects will perform EOS visit.
- A subject whose wound is not deemed closed (epithelialized with no drainage) by physician at week 12 will exit from the study after the week 12 wound evaluation.
- Assess index ulcer.
- If wound has not closed, perform standardized photography of the study wound.
- If wound has not closed, assess the ulcer area (cm2), perimeter (cm), and greatest depth (cm) using the inSight device.
- Perform hyperspectral imaging of the dorsal and plantar aspects of the foot if wound is active or healed.
- If wound has not closed, redress the wound per physician-directed standard of care.
- Administer Patient Reported Outcome (PRO) (questionnaires).
- Collect all relevant concomitant medication
- Perform EOS visit documentation
- Follow up on AE/SAEs that have been reported that have not yet been resolved.
Study Visit Follow-up:
- If the wound heals during the treatment phase or if the wound is not healed after 12 weeks, data from their electronic medical record will be evaluated to identify healing, time to heal, adverse events related to the wound.
- Conditions
- Diabetic Wound
- Being tested
- NPWT and lyopreserved Stravix, NPWT and cryopreserved Stravix
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
NPWT and lyopreserved StravixDevice
Subjects will be treated with NPWT and lyopreserved Stravix
NPWT and cryopreserved StravixDevice
Subjects will be treated with NPWT and lyopreserved Stravix
| Study group | Role | What they receive |
|---|---|---|
| Lyopreserved Stravix | Active comparator | Treated with NPWT and lyopreserved Stravix Receives: Device: NPWT and lyopreserved Stravix |
| Cryopreserved Stravix | Active comparator | Treated with NPWT and cryopreserved Stravix Receives: Device: NPWT and cryopreserved Stravix |
What is being measured
The primary outcome is the main question the study is designed to answer.
Complete Wound Closure
Number of patients who achieve wound closure (complete epithelialization with no drainage)
Measured: 12 weeks
Secondary outcomes (3)
Duration of Negative Pressure Wound Therapy
Number of days patient received negative pressure wound therapy after application of Stravix
Measured: 12 weeks
Split Thickness Skin Grafting
Number of patients who received a split thickness skin graft
Measured: 12 weeks
Infection
Number of patients who developed infection
Measured: 12 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted28 May 2020
- Study start22 Jun 2021
- Primary completion7 Jul 2022
- Study completion7 Jul 2022
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Other trials for Diabetic WoundStudies of the same condition, open and under way.
- More trials run by University of Texas Southwestern Medical CenterThe sponsor's other registered studies.
- 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
- Interventional
- Phase
- Phase 4
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- Prospective, 2-arm parallel assignment, randomized clinical trial. Stravix will be applied at initial visit with NPWT and will only be reapplied after 4 weeks if wound is not ready for grafting unless debridement is indicated.
- Masking
- None (open label)
- Enrolment
- 46 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Texas Southwestern Medical Center
- Sponsor type
- University, hospital or other
- Collaborators
- Osiris Therapeutics
- Responsible party
- Principal investigator, Larry Lavery, University of Texas Southwestern Medical Center
- Investigators
- Lawrence Lavery, DPM MPH, Principal investigator, University of Texas Southwestern Medical Center
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04405765
- Sponsor's protocol ID
- 2020-0293
- Status last verified
- Jul 2023
- First submitted
- 22 May 2020
- Last updated
- 24 Jul 2023
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- Yes
Study at a glance
From the registry record, last updated by the sponsor on 24 Jul 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Prospective, Randomized, Single-Center Study to Compare Clinical Outcomes Between Cryopreserved and Lyopreserved Stravix as an Adjunct to NPWT in the Treatment of Complex Wounds
- ClinicalTrials.gov ID
- NCT04405765
- Acronym / sponsor ID
- 2020-0293
- Conditions
- Diabetic Wound
- Phase
- Phase 4
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 46 participants (actual)
- Lead sponsor
- University of Texas Southwestern Medical CenterUniversity, hospital or other
- Collaborators
- Osiris Therapeutics
- Study start
- 22 Jun 2021 (actual)
- Primary completion
- 7 Jul 2022 (actual)
- Study completion
- 7 Jul 2022 (actual)
- First posted
- 28 May 2020 (actual)
- Results
- Posted 18 May 2023
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This study is a prospective, 2-arm parallel assignment, randomized clinical trial to compare lyopreserved vs cryopreserved Stravix as an adjunct therapy to NPWT.
Detailed description
Screening
- Explain purpose and nature of the study and obtain signature on the informed consent document.
- Screen the subject against protocol inclusion and exclusion criteria, including all pertinent tests, including pregnancy test 3. Complete SF-36, EuroQol 5 dimensions (EQ-5D) and PROMIS® Baseline (may be done as same day as screening procedures or within +2 days of screening and before start of Therapy/Treatment Phase)
- Obtain general medical history and demographic information and social history
- Complete a physical examination, body weight, height, and vital signs, including measurement of resting heart rate, respiratory rate, and blood pressure while seated.
- Select target study ulcer
- Obtain complete history pertinent to DFU disease including duration of the target ulcer, previous and current treatment. Document ulcer classification.
- Perform debridement and obtain tissue collection (3 tissue and 1 bone).
- Perform standardized photography and measurement of the study wound (eKare or available camera with ruler). Assess the post-debridement ulcer area (cm2), perimeter (cm), and greatest depth (cm) using the inSight device (eKare, Fairfax, VA). These values are the baseline measurements for calculating wound closure rate at the two-week run-in visit.
- Perform hyperspectral imaging of dorsal and plantar aspects of the foot.
- Perform neuropathy assessment
- Collect all relevant concomitant medication (antibiotics, antifungals and other anti-infective therapies)
- Place Stravix (lyo or cryo per randomization schedule) and dress wound for NPWT therapy.
- Document size of Stravix used.
- Disburse subject stipend Therapy/Treatment Phase (Weekly visits +/- 4 days)
Study Visit 1-11:
- Assess target ulcer (if wound has closed, document as such, skip to step 5).
- Document time on/off NPWT if applicable.
- Perform standardized photography of the study wound when NPWT is removed.
- If Stravix is removed, assess the ulcer area (cm2), perimeter (cm), and greatest depth (cm) using the inSight device - if the wound is deemed closed by the physician, skip to EOS visit.
- Perform hyperspectral imaging of the dorsal and plantar aspects of the foot if wound is active or closed.
- Debride wound if indicated. Re-measure wound if surgical debridement is performed prior to dressing the wound.
- Collect all relevant concomitant medication.
- If wound is still active, redress the wound with assigned Stravix (if removed for debridement) and NPWT. Document all dressings applied including size of Stravix.
- Disburse subject stipend
- Note: at week 4, if wound is not ready for grafting, remove existing Stravix and replace with new piece of Stravix (per randomization schedule)
- Assess for AE/SAEs and/or follow up on previous AE/SAEs.
Study Visit Closed 1. When a subject's study wound has closed, they will perform the EOS evaluation.
Study Visit 12/EOS:
- At the time of wound closure, subjects will perform EOS visit.
- A subject whose wound is not deemed closed (epithelialized with no drainage) by physician at week 12 will exit from the study after the week 12 wound evaluation.
- Assess index ulcer.
- If wound has not closed, perform standardized photography of the study wound.
- If wound has not closed, assess the ulcer area (cm2), perimeter (cm), and greatest depth (cm) using the inSight device.
- Perform hyperspectral imaging of the dorsal and plantar aspects of the foot if wound is active or healed.
- If wound has not closed, redress the wound per physician-directed standard of care.
- Administer Patient Reported Outcome (PRO) (questionnaires).
- Collect all relevant concomitant medication
- Perform EOS visit documentation
- Follow up on AE/SAEs that have been reported that have not yet been resolved.
Study Visit Follow-up:
- If the wound heals during the treatment phase or if the wound is not healed after 12 weeks, data from their electronic medical record will be evaluated to identify healing, time to heal, adverse events related to the wound.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
- Model description
- Prospective, 2-arm parallel assignment, randomized clinical trial. Stravix will be applied at initial visit with NPWT and will only be reapplied after 4 weeks if wound is not ready for grafting unless debridement is indicated.
| Arm | Type | Receives |
|---|---|---|
| Lyopreserved Stravix | Active comparator | Device: NPWT and lyopreserved StravixTreated with NPWT and lyopreserved Stravix |
| Cryopreserved Stravix | Active comparator | Device: NPWT and cryopreserved StravixTreated with NPWT and cryopreserved Stravix |
Who may qualify
- Ages
- 21 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (5 listed)
- Diagnosis of a diabetes mellitus
- Men/women ≥21 years old
- Post-operative foot or ankle wounds sized >4cm2 that have presented for <1 year
- ABI ≥0.5 or toe pressures >30 mmHg
- Wounds indicated for treatment with NPWT
Key exclusion criteria (7 listed)
- Active Charcot arthropy
- Unable to use NPWT at home
- Untreated bone or soft tissue infection
- Is pregnant or plans to become pregnant
- Is nursing or actively lactating
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 |
|---|---|---|
| NPWT and lyopreserved StravixSubjects will be treated with NPWT and lyopreserved Stravix | Device | Lyopreserved Stravix |
| NPWT and cryopreserved StravixSubjects will be treated with NPWT and lyopreserved Stravix | Device | Cryopreserved Stravix |
Primary outcome
Complete Wound Closure
Time frame: 12 weeks
Number of patients who achieve wound closure (complete epithelialization with no drainage)
3 secondary outcomes
Duration of Negative Pressure Wound Therapy
Time frame: 12 weeks
Split Thickness Skin Grafting
Time frame: 12 weeks
Infection
Time frame: 12 weeks
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 24 Jul 2023.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
Related trials for Diabetic Wound
Recruiting
PAW-Hydrogel for Chronic Wound Healing
Diabetic Foot Ulcer (DFU), Pressure Ulcer (PU)
Active, not recruiting
Evaluation of Personalized Nutritional Intervention on Wound Healing of Cutaneous Ulcers in Diabetics
Foot, Diabetic
Active, not recruiting
EDX110 Randomized Control Trial for Treatment of DFUs
Wound Heal, Diabetic Foot Ulcer
Active, not recruiting
Impact of Screening and Multicomponent Exercise on Fall Rates, Fractures, and Cardiovascular Health in Diabetes
Type 2 Diabetes, Osteoporosis
Not yet recruiting
Comparison of Negative Pressure Wound Therapy Versus Moist Wound Dressing in Diabetic Foot Ulcer Patients
Diabetic Foot Ulcer
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.
Lawrence Lavery, DPM MPH principal investigator
University of Texas Southwestern Medical Center
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 4 study testing NPWT and lyopreserved Stravix and NPWT and cryopreserved Stravix in people with Diabetic Wound, run by University of Texas Southwestern Medical Center at 1 site 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 5 inclusion and 7 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: finished, as of the sponsor's last update on 24 Jul 2023. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site 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.
What does this phase mean?
Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
Yes. Results are posted in the registry (first posted 18 May 2023). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.
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?
Complete Wound Closure (time frame: 12 weeks). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
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 24 Jul 2023.