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Wound InfectionPhase 4NCT03686904

Investigation of a Novel Wound Gel to Improve Wound Healing in Chronic Wounds

A Phase 4 study testing Benzalkonium Gel, Debridement and benzalkonium irrigation in people with Wound Infection, run by Georgetown University 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 is a prospective, randomized, double-blinded, single site study examining the impact of a biofilm-based treatment of chronic wounds of the lower extremity. 200 subjects will be enrolled in this study. Read more about this study

Who is it for?
Ages 18 to 99 years
Conditions the study is for
Wound Infection
What is being tested?
Benzalkonium Gel, Debridement and benzalkonium irrigation
Type of treatment
Surgery or procedure
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
11 participants
Where
1 siteUnited States
Study dates
19 Nov 2018to 14 Feb 2020
Phase
Phase 4
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 to 99 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Male or female, aged 18-99
  • Chronic wound requiring debridement
  • Wound located anywhere on the body
  • Able to comply with clinical trial requirements

Who cannot join

  • Patient unable or unwilling to comply with study requirements
  • Disease or treatment causing substantial immunosuppression
  • History of allergic reaction to benzalkonium
  • Transplant recipient

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Medstar Georgetown University Hospital

    Washington D.C., District of Columbia, 20007

Other trials in United States

About this study

Official title: Investigating the Effect of an Anti-Biofilm Solution to Reduce Bacterial Burden and Accelerate Healing in Chronic Wounds.

This is a prospective, randomized, double-blinded, single site study examining the impact of a biofilm-based treatment of chronic wounds of the lower extremity. 200 subjects will be enrolled in this study. Benzalkonium solution wound irrigation and Benzalkonium wound gel will be compared to standard of care wound preparation and dressing (NS wound irrigation and hydrocolloid gel) following local debridement. Wounds will be assessed maximum of 12 weeks with a minimum of 4 follow up visits. Patients will be recruited from the general wound clinic population. No enticement will be offered and participation will be completely voluntary. At enrollment and at each follow up visit the wound will be assessed for size (length, width, and depth), signs of infection or irritation, qualitative and quantitative cultures will be taken before and after debridement, patients will be assessed for compliance to the treatment protocol, satisfaction with their treatment, any adverse effects of the treatment, and hospitalizations since last assessment. It is anticipated that enrollment and completion of the study will take 1 year.

Read the detailed description

The role of biofilm in causing wound infections and preventing healing is unclear. Preliminary data suggests that persistent biofilm following excisional debridement may re-inoculate clean wounds leading to infection. Additionally, this data also suggests that persistent biofilm leads to chronic wound inflammation. Novel wound gels have been developed which claim to disrupt biofilm and kill biofilm producing bacteria. Patients presenting with a chronic wound will be randomized to receive treatment with a novel anti-biofilm solution BlastX™(benzalkonium gel) or standard of care. All patients presenting with a chronic wound (>4 weeks duration) will be assessed for eligibility in the study. If eligible, subjects will be randomized into Cohort A (debridement, NS irrigation, SOC topical wound treatment), Cohort B (debridement, benzalkonium irrigation, SOC topical wound treatment), Cohort C (debridement, NS irrigation, and benzalkonium topical wound treatment) of Cohort D (debridement, benzalkonium irrigation, and benzalkonium topical wound treatment). Subjects will receive this treatment until the wound is completely healed or they are exited from the study.

Infection of chronic wounds is a multifactorial process involving the interplay between host factors, the condition of the wound, and the number and virulence of bacterial species that flourish and critically colonize in the tissue. 1 It is widely recognized that the microorganisms colonizing in these wounds are biofilm producers. 2, 3, 4, 5 Biofilm is a polymeric slime layer made up of polymeric sugars, microbial and/or host DNA, microbial proteins and host molecules that encapsulate microorganisms.5 This limits the reach of the host immune system and antibacterial agents. Biofilm formation has been associated with the emergence of a diverse group of opportunistic pathogens, such as Staphylococcus aureus and Pseudomonas aeruginosa, which contribute to recurrent infections by modifying environmental parameters.4

Excisional debridement is the standard of care for chronic wound management and has shown to be effective against biofilm. However, studies have shown that biofilm formation recurs within 24hrs of debridement. Common topical wound preparations contain silver, iodine, honey, or chlorhexidine; none of which have shown efficacy against biofilm.1 Recent studies have reported that when targeting and disrupting the wound biofilm matrix, wound healing outcomes are improved and there is a significant decrease in biofilm-related infections. 3, 5 To date, there is no widely accepted topical agent which targets biofilm.

Preliminary and invitro studies have shown benzalkonium chloride to be an effective agent to disrupt biofilm and prevent recolonization. An example of a commercially available formulation of benzalkonium chloride is Benzalkonium gel wound gel and Benzalkonium solution wound irrigation. There is insufficient clinical data suggesting whether a biofilm focused approach is superior or inferior to standard of care treatment. In order to determine the clinical efficacy of a biofilm-focused approached against current stand of care treatment, this study outlines a clinical study evaluating the outcomes of patients treated with Benzalkonium gel and Benzalkonium solution compared to standard of care wound gel and irrigation.

Conditions
Wound Infection
Being tested
Benzalkonium Gel, standard of care topical gel, Debridement, benzalkonium irrigation, Saline Irrigation (SOC Irrigation)
Medical subject headings
Wound Infection

What participants receive

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

  • Benzalkonium GelDrug

    Also called BlastX

    antibiofilm solution (BlastX) topical wound gel

  • standard of care topical gelOther

    Also called Topical Antibacterial gel

    standard of care topical gel (hydrocolloid topical gel)

  • DebridementProcedure or surgery

    Also called local debridement

    Removing dead tissue from infected wound (in clinic)

  • benzalkonium irrigationDrug

    Also called TorrentX

    washing and lavaging in clinic with benzalkonium irrigation

  • Saline Irrigation (SOC Irrigation)Other

    Also called SOC Irrigation

    Normal Saline Irrigation (SOC Irrigation)

Study groups in NCT03686904
Study groupRoleWhat they receive
SOC GROUP [Cohort A]Placebo comparatorDebridement, SOC irrigation \& SOC topical gel
Receives: Other: standard of care topical gel; Procedure: Debridement; Other: Saline Irrigation (SOC Irrigation)
SOC TOPICAL GEL & TORRENT X GROUP [Cohort B]Active comparatorDebridement, benzalkonium irrigation \& SOC topical gel
Receives: Other: standard of care topical gel; Procedure: Debridement; Drug: benzalkonium irrigation
BLASTX and SALINE (SOC) GROUP [Cohort C]Active comparatorDebridement, SOC saline irrigation \& benzalkonium gel
Receives: Drug: Benzalkonium Gel; Procedure: Debridement; Other: Saline Irrigation (SOC Irrigation)
BLASTX and TORRENTX GROUP [Cohort D]Active comparatorDebridement, benzalkonium irrigation \& benzalkonium gel
Receives: Drug: Benzalkonium Gel; Procedure: Debridement; Drug: benzalkonium irrigation

What is being measured

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

  1. Colony Forming Units Count Measure (Primary Measure)

    The primary outcome is the change in CFU counts after treatment with Benzalkonium solution/Benzalkonium gel or SOC.

    Measured: 12 weeks

Secondary outcomes (2)
  1. Change in index ulcer size measured in cm squared (Secondary endpoints)

    Change in index ulcer size measured in cm squared

    Measured: 12 weeks

  2. Duration of index ulcer measured in weeks (Secondary endpoints)

    Duration of index ulcer measured in weeks

    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 posted27 Sep 2018
  2. Study start19 Nov 2018
  3. Primary completion14 Feb 2020
  4. Study completion14 Feb 2020

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
Masking
Single blind
Who is masked
Participant
Enrolment
11 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03686904
Sponsor's protocol ID
2018-0218
Status last verified
Jan 2020
First submitted
2 Aug 2018
Last updated
2 Jun 2022
Results posted
No
Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
No: Data was not collected for use in future research and will not be shared

Questions about this trial

What is this clinical trial studying?

A Phase 4 study testing Benzalkonium Gel, Debridement and benzalkonium irrigation in people with Wound Infection, run by Georgetown University 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 4 inclusion and 4 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 2 Jun 2022. 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. Some participants in this study may receive a placebo. 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?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

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?

Colony Forming Units Count Measure (Primary Measure) (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 2 Jun 2022.

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