PluroGel on Wounds of Mixed Etiology

Venous Ulcer Clinical Trial

Official title:

A Pilot Study to Investigate the Efficacy of PluroGel in Healing Venous and Mixed Aetiology Leg Ulcers

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT03275831
• Other study ID #: R17-006
• Secondary ID: WWIC/2016/02
• Status: Terminated
• Phase: N/A
• Start date: January 8, 2018
• Est. completion date: October 5, 2021

Study information

• Verified date: October 2021
• Source: Medline Industries
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

A randomized controlled study (RCT) to investigate the topical effectiveness of PluroGel in healing venous and mixed aetiology leg ulcers. Patients with venous and mixed aetiology leg ulcers will be identified from hospital outpatient clinics. Willing patients meeting the inclusion and exclusion criteria will be consented and assessed in line with standard care. Participants will be randomized at Week 2 to receive either topical PluroGel or Intrasite gel (an alternative topical hydrogel product) if inclusion criteria is met.

Description:

This will be a pilot, randomized, controlled, multi-center trial to determine the effectiveness of PluroGel in the reduction of size of wounds and reduction of slough covering the wound surface compared with Intrasite Gel. The primary objectives will be to evaluate the effectiveness of PluroGel compared with Intrasite Gel in the reduction of size of venous leg ulcers or mixed venous arterial aetiology. Also the reduction in the percentage of slough covering the wound bed in both groups will be compared. The secondary objective will be to evaluate patient comfort, satisfaction and acceptance of the hydrogels along with staff feedback of both hydrogels. Patients with either a venous leg ulcer (VLU) or an mixed venous arterial aetiology (MAU) leg ulcer will be identified by the participant's health care provider and will be treated with PluroGel or Intrasite Gel. A total of 40 subjects will be enrolled to the study, 20 to each arm. These subjects will be recruited from patients receiving treatment for wounds at NHS outpatient clinic. Participants will be approached initially by the NHS care-giver and asked if interested in participating in research. If interested, participants will be asked to sign a permission to contact form for contact details to be given to a member of the research team who would then contact the participant to provide further information. A screening log will be kept of all patients who have been considered but who do not fulfill the criteria for entry. Patients will be randomized to either Plurogel and standard care or Intrasite Gel in conjunction with standard care, on an equal basis. Subjects will be eligible for randomization if during the first two weeks within the study the target wound has not reduced in surface area by 30% or more and there has been a less than 25% reduction in the cover of the wound bed with visible slough. Once the subject has completed 4-weeks of treatment, and the final visit, or the target ulcer has healed, whichever is soonest, then the subject has completed the study and the termination form will be completed. The Investigator will ensure that all CRF forms are completed and accurate. The study end date will be the date of the last subject's last visit. The CI and study sponsor, will comply with any safety reporting obligations for serious adverse device related events to the manufacturer, study sponsor, R&D Department(s) of the University Health Board(s) and the Ethics Committee, as defined in the applicable laws and regulations, and within the required timelines.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 16
• Est. completion date: October 5, 2021
• Est. primary completion date: October 5, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patients aged = 18 years old

• Patients with a non-healing venous leg ulcer or mixed aetiology ulcer.

• Duration of wound = 6 weeks = 5 years

• Wound is = 1 cm2 = 100cm2 no length longer than 10cm

• Presence of at least 25% visible slough within the wound bed

• The patient must be able to understand the study and provide written informed consent

• No clinical signs of infection

Exclusion Criteria:

• Known hypersensitivity to any of the wound dressings or compression bandaging to be used in the trial

• Current local or systemic antibiotics in the week prior to inclusion

• Clinically infected wound as determined by the presence of 3 or more of the following clinical signs: perilesional erythema, pain between two dressing changes, malodorous wound, abundant exudate and oedema.

• Prolonged treatment with immunosuppressive agents or high dose corticosteroids

• Patients who have a current illness or condition which may interfere with wound healing in the last 30 days (carcinoma, connective tissue disease, autoimmune disease or alcohol or drug abuse)

• Patients who have participated in a clinical trial on wound healing within the past month

• Patients with a known history of non-adherence with medical treatment

Related Conditions & MeSH terms

• Arterial Ulcer
• Ulcer
• Varicose Ulcer
• Venous Ulcer

Intervention

Device:
• PluroGel
Surfactant based gel
• Intrasite gel
Hydrogel

Locations

Country	Name	City	State
United Kingdom	Cardiff & Vale University Health Board	Cardiff	Wales
United Kingdom	Aneurin Bevan University Health Board	Newport	South Wales

Sponsors (1)

Lead Sponsor	Collaborator
Medline Industries

Country where clinical trial is conducted

United Kingdom, 

References & Publications (5)

Callam MJ, Harper DR, Dale JJ, Ruckley CV. Arterial disease in chronic leg ulceration: an underestimated hazard? Lothian and Forth Valley leg ulcer study. Br Med J (Clin Res Ed). 1987 Apr 11;294(6577):929-31. — View Citation

Connor-Ballard PA. Understanding and managing burn pain: Part 2. Am J Nurs. 2009 May;109(5):54-62; quiz 63. doi: 10.1097/01.NAJ.0000351510.77627.db. Review. — View Citation

Cullum N, Nelson EA, Fletcher AW, Sheldon TA. Compression for venous leg ulcers. Cochrane Database Syst Rev. 2000;(3):CD000265. Review. Update in: Cochrane Database Syst Rev. 2001;(2):CD000265. — View Citation

Gottrup F, Apelqvist J, Price P; European Wound Management Association Patient Outcome Group. Outcomes in controlled and comparative studies on non-healing wounds: recommendations to improve the quality of evidence in wound management. J Wound Care. 2010 Jun;19(6):237-68. — View Citation

Hunter RL, Luo AZ, Zhang R, Kozar RA, Moore FA. Poloxamer 188 inhibition of ischemia/reperfusion injury: evidence for a novel anti-adhesive mechanism. Ann Clin Lab Sci. 2010 Spring;40(2):115-25. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in wound size	Comparison of change in wound surface area (cm2) over a 4 week assessment between baseline and final assessment in PluroGel treated group compared to Intrasite treated group.	4 weeks
Primary	Change in average percent reduction of slough in wound bed over 4 week treatment	Comparison of change in average percent reduction of slough present in the wound bed observed at baseline and over 4 week treatment period in PluroGel treated group compared to Intrasite treated group	4 weeks
Secondary	Patient evaluation	Survey questions to report adherence to protocol of care, comfort, comparison with previous treatments, level of patient discomfort and pain during use of either PluroGel or Intrasite	Up to 6 weeks
Secondary	Staff evaluation	Survey to record staff feedback including ease of application and removal of both PluroGel and the comparator Intrasite.	Up to 6 weeks