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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.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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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

Other trials in United States

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

  1. Explain purpose and nature of the study and obtain signature on the informed consent document.
  2. 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)
  3. Obtain general medical history and demographic information and social history
  4. Complete a physical examination, body weight, height, and vital signs, including measurement of resting heart rate, respiratory rate, and blood pressure while seated.
  5. Select target study ulcer
  6. Obtain complete history pertinent to DFU disease including duration of the target ulcer, previous and current treatment. Document ulcer classification.
  7. Perform debridement and obtain tissue collection (3 tissue and 1 bone).
  8. 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.
  9. Perform hyperspectral imaging of dorsal and plantar aspects of the foot.
  10. Perform neuropathy assessment
  11. Collect all relevant concomitant medication (antibiotics, antifungals and other anti-infective therapies)
  12. Place Stravix (lyo or cryo per randomization schedule) and dress wound for NPWT therapy.
  13. Document size of Stravix used.
  14. Disburse subject stipend Therapy/Treatment Phase (Weekly visits +/- 4 days)

Study Visit 1-11:

  1. Assess target ulcer (if wound has closed, document as such, skip to step 5).
  2. Document time on/off NPWT if applicable.
  3. Perform standardized photography of the study wound when NPWT is removed.
  4. 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.
  5. Perform hyperspectral imaging of the dorsal and plantar aspects of the foot if wound is active or closed.
  6. Debride wound if indicated. Re-measure wound if surgical debridement is performed prior to dressing the wound.
  7. Collect all relevant concomitant medication.
  8. 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.
  9. Disburse subject stipend
  10. Note: at week 4, if wound is not ready for grafting, remove existing Stravix and replace with new piece of Stravix (per randomization schedule)
  11. 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:

  1. At the time of wound closure, subjects will perform EOS visit.
  2. 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.
  3. Assess index ulcer.
  4. If wound has not closed, perform standardized photography of the study wound.
  5. If wound has not closed, assess the ulcer area (cm2), perimeter (cm), and greatest depth (cm) using the inSight device.
  6. Perform hyperspectral imaging of the dorsal and plantar aspects of the foot if wound is active or healed.
  7. If wound has not closed, redress the wound per physician-directed standard of care.
  8. Administer Patient Reported Outcome (PRO) (questionnaires).
  9. Collect all relevant concomitant medication
  10. Perform EOS visit documentation
  11. Follow up on AE/SAEs that have been reported that have not yet been resolved.

Study Visit Follow-up:

  1. 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 groups in NCT04405765
Study groupRoleWhat they receive
Lyopreserved StravixActive comparatorTreated with NPWT and lyopreserved Stravix
Receives: Device: NPWT and lyopreserved Stravix
Cryopreserved StravixActive comparatorTreated 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.

  1. Complete Wound Closure

    Number of patients who achieve wound closure (complete epithelialization with no drainage)

    Measured: 12 weeks

Secondary outcomes (3)
  1. Duration of Negative Pressure Wound Therapy

    Number of days patient received negative pressure wound therapy after application of Stravix

    Measured: 12 weeks

  2. Split Thickness Skin Grafting

    Number of patients who received a split thickness skin graft

    Measured: 12 weeks

  3. 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.

  1. First posted28 May 2020
  2. Study start22 Jun 2021
  3. Primary completion7 Jul 2022
  4. Study completion7 Jul 2022

Resources

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)
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
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
Yes

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.

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