NCT06000722

Brief Summary

Background: People with diabetes and either current or previous diabetic foot ulcer disease (DFUD) are at very high risk for adverse cardiovascular events including heart attacks and strokes. Sodium-glucose co-transporter 2 (SGLT2) inhibitors are a class of medications that have shown to be very effective in reducing heart disease and event risk. However, one recent study found that SGLT2i's may increase minor amputation risk in those with DFUD, though this finding has not been replicated in other similar studies. However, as a result, there has been limited further investigation into this issue and as such the use of SGLT2i's in those with DFUD remains a contentious issue, despite their potential for significantly reducing cardiovascular disease risk in this population. In the absence of further randomised controlled trials investigating the use of SGLT2is in these populations, there is a need for clinical guidelines advising on their use based on expert clinical consensus, including specific criteria or scenarios in which they should or should not be used. The Delphi methodology is an iterative survey technique that uses expert opinion from various relevant backgrounds and experiences to generate a consensus based upon various statements and/or scenarios. Aim: The aim of this study is to use the Delphi technique to generate expert consensus-based clinical guidelines on the use of SGLT2i's in those with diabetes and DFUD. Methods: This is a Delphi technique-based study using a purposive sample of convenience. Consensus development methods will be used to generate clinical guidelines, endorsed by key clinical groups, on the use of SGLT2i's in patients with diabetic foot ulcer disease, including acknowledgement of specific scenarios or patient characteristics that may influence these guidelines. The consensus group will consist of n=20 healthcare practitioners, including GPs, secondary care diabetologists, foot care specialists, cardiologists and pharmacists in order to ensure a breadth of expertise and input. Two rounds of the Delphi consensus process will take place, in order to iteratively develop the consensus-based clinical guidelines. This process is expected to take 4-6 months. The analysis will be on-going throughout the study and completed within 3 months of the last questionnaire round of the Delphi process.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
21

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Dec 2023

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

August 14, 2023

Completed
7 days until next milestone

First Posted

Study publicly available on registry

August 21, 2023

Completed
4 months until next milestone

Study Start

First participant enrolled

December 5, 2023

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 28, 2024

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

April 30, 2024

Completed
Last Updated

May 8, 2024

Status Verified

May 1, 2024

Enrollment Period

3 months

First QC Date

August 14, 2023

Last Update Submit

May 7, 2024

Conditions

Outcome Measures

Primary Outcomes (2)

  • Delphi Round 1

    Each participant will provided with the clinical statements regarding the use of SGLT2i's in patients with diabetic foot ulcer disease, and sent the link to an online questionnaire. Within the first questionnaire round the participants will be asked to rate these statements i.e. strongly agree, agree, uncertain (probably agree), uncertain (probably disagree), disagree, strongly disagree. Participants will be given three weeks to complete this questionnaire, and will be sent reminder emails during this time. This will establish priorities amongst the statements listed. As a result of completing round one, areas of disagreement and agreement will be identified and a level of consensus will begin to form.

    3 weeks

  • Delphi Round 2

    The second round of the questionnaire will consist of a summary of the items and ratings from the previous round. Participants will be asked to revise his/her judgments or to specify why they wish to remain outside of the consensus. This round gives the Delphi participants an opportunity to make further clarifications of both the information \& their judgment of the relative importance of the items. Round 2 will be initiated 1 month after the completion of round 1. If consensus is not reached on the majority of statements following round 2, and third and final round may be added in order to reach consensus.

    3 weeks

Study Arms (1)

Healthcare practitioners

Participants who are trained healthcare practitioners involved in the care of patients with current or previous diabetic foot ulcer disease

Other: eDelphi method

Interventions

This is a Delphi technique-based study using a purposive sample of convenience. Consensus development methods will be used to generate clinical guidelines, endorsed by key clinical groups, on the use of SGLT2i's in patients with diabetic foot ulcer disease, including acknowledgement of specific scenarios or patient characteristics that may influence these guidelines.

Healthcare practitioners

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Participants in the Delphi study will consist of n=20 healthcare practitioners and will be recruited from a convenience sample, and representing a range of specialties and clinical backgrounds.

You may qualify if:

  • Participants who are trained healthcare practitioners involved in the care of patients with current or previous diabetic foot ulcer disease

You may not qualify if:

  • Potential participants who do not give informed consent. Potential participants who will not be able to participate in both rounds of the Delphi process.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Leicester

Leicester, United Kingdom

Location

MeSH Terms

Conditions

Diabetic Foot

Condition Hierarchy (Ancestors)

Diabetic AngiopathiesVascular DiseasesCardiovascular DiseasesFoot UlcerLeg UlcerSkin UlcerSkin DiseasesSkin and Connective Tissue DiseasesDiabetes ComplicationsDiabetes MellitusEndocrine System DiseasesDiabetic Neuropathies

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 14, 2023

First Posted

August 21, 2023

Study Start

December 5, 2023

Primary Completion

February 28, 2024

Study Completion

April 30, 2024

Last Updated

May 8, 2024

Record last verified: 2024-05

Locations