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.
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
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 group | Role | What they receive |
|---|---|---|
| SOC GROUP [Cohort A] | Placebo comparator | Debridement, 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 comparator | Debridement, 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 comparator | Debridement, SOC saline irrigation \& benzalkonium gel Receives: Drug: Benzalkonium Gel; Procedure: Debridement; Other: Saline Irrigation (SOC Irrigation) |
| BLASTX and TORRENTX GROUP [Cohort D] | Active comparator | Debridement, 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.
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)
Change in index ulcer size measured in cm squared (Secondary endpoints)
Change in index ulcer size measured in cm squared
Measured: 12 weeks
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.
- First posted27 Sep 2018
- Study start19 Nov 2018
- Primary completion14 Feb 2020
- Study completion14 Feb 2020
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Wound InfectionStudies of the same condition, open and under way.
- More trials run by Georgetown UniversityThe 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
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 11 participants (actual)
Sponsor and investigators
- Lead sponsor
- Georgetown University
- Sponsor type
- University, hospital or other
- Collaborators
- Next Science TM
- Responsible party
- Sponsor
- Investigators
- Christopher Attinger, MD, Principal investigator, MedStar Georgetown University Hospital
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
Study at a glance
From the registry record, last updated by the sponsor on 2 Jun 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Investigating the Effect of an Anti-Biofilm Solution to Reduce Bacterial Burden and Accelerate Healing in Chronic Wounds.
- ClinicalTrials.gov ID
- NCT03686904
- Acronym / sponsor ID
- 2018-0218
- Conditions
- Wound Infection
- Phase
- Phase 4
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 11 participants (actual)
- Lead sponsor
- Georgetown UniversityUniversity, hospital or other
- Collaborators
- Next Science TM
- Study start
- 19 Nov 2018 (actual)
- Primary completion
- 14 Feb 2020 (actual)
- Study completion
- 14 Feb 2020 (actual)
- First posted
- 27 Sep 2018 (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.
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.
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.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (participant)
- Number of arms
- 4
| Arm | Type | Receives |
|---|---|---|
| SOC GROUP [Cohort A] | Placebo comparator | Other: standard of care topical gel, Procedure: Debridement, Other: Saline Irrigation (SOC Irrigation)Debridement, SOC irrigation \& SOC topical gel |
| SOC TOPICAL GEL & TORRENT X GROUP [Cohort B] | Active comparator | Other: standard of care topical gel, Procedure: Debridement, Drug: benzalkonium irrigationDebridement, benzalkonium irrigation \& SOC topical gel |
| BLASTX and SALINE (SOC) GROUP [Cohort C] | Active comparator | Drug: Benzalkonium Gel, Procedure: Debridement, Other: Saline Irrigation (SOC Irrigation)Debridement, SOC saline irrigation \& benzalkonium gel |
| BLASTX and TORRENTX GROUP [Cohort D] | Active comparator | Drug: Benzalkonium Gel, Procedure: Debridement, Drug: benzalkonium irrigationDebridement, benzalkonium irrigation \& benzalkonium gel |
Who may qualify
- Ages
- 18 to 99 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- Male or female, aged 18-99
- Chronic wound requiring debridement
- Wound located anywhere on the body
- Able to comply with clinical trial requirements
Key exclusion criteria (4 listed)
- Patient unable or unwilling to comply with study requirements
- Disease or treatment causing substantial immunosuppression
- History of allergic reaction to benzalkonium
- Transplant recipient
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 |
|---|---|---|
| Benzalkonium GelAlso: BlastXantibiofilm solution (BlastX) topical wound gel | Drug | BLASTX and SALINE (SOC) GROUP [Cohort C], BLASTX and TORRENTX GROUP [Cohort D] |
| standard of care topical gelAlso: Topical Antibacterial gelstandard of care topical gel (hydrocolloid topical gel) | Other | SOC GROUP [Cohort A], SOC TOPICAL GEL & TORRENT X GROUP [Cohort B] |
| DebridementAlso: local debridementRemoving dead tissue from infected wound (in clinic) | Procedure or surgery | BLASTX and SALINE (SOC) GROUP [Cohort C], BLASTX and TORRENTX GROUP [Cohort D], SOC GROUP [Cohort A], SOC TOPICAL GEL & TORRENT X GROUP [Cohort B] |
| benzalkonium irrigationAlso: TorrentXwashing and lavaging in clinic with benzalkonium irrigation | Drug | BLASTX and TORRENTX GROUP [Cohort D], SOC TOPICAL GEL & TORRENT X GROUP [Cohort B] |
| Saline Irrigation (SOC Irrigation)Also: SOC IrrigationNormal Saline Irrigation (SOC Irrigation) | Other | BLASTX and SALINE (SOC) GROUP [Cohort C], SOC GROUP [Cohort A] |
Primary outcome
Colony Forming Units Count Measure (Primary Measure)
Time frame: 12 weeks
The primary outcome is the change in CFU counts after treatment with Benzalkonium solution/Benzalkonium gel or SOC.
2 secondary outcomes
Change in index ulcer size measured in cm squared (Secondary endpoints)
Time frame: 12 weeks
Duration of index ulcer measured in weeks (Secondary endpoints)
Time frame: 12 weeks
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 2 Jun 2022.
- Individual participant dataSharing planned: No. Data was not collected for use in future research and will not be shared
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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.
Christopher Attinger, MD principal investigator
MedStar Georgetown University Hospital
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 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.