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Sealed Therapeutic Shoe as Treatment of Diabetic Foot Ulcers

R

Region Örebro County

Status

Terminated

Conditions

Diabetic Foot

Treatments

Device: Total contact cast
Device: Sealed therapeutic shoe

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT04085926
18RS6667

Details and patient eligibility

About

Total contact casts (TCCs) are effective treatment of plantar diabetic foot ulcers because they effectively offload the ulcer and are non-removable, resulting in high adherence to using the device. However, TCCs are not widely used in clinical practice because they negatively impact gait and daily activities. A new treatment concept was invented, sealed therapeutic shoe, where a shoe with a custom-made insole offloads the ulcer, and the shoe is rendered irremovable to be worn day and night, like a TCC.

In this multicenter randomized controlled trial (RCT), 150 participants will be recruited and randomized to two treatment arms: TCC or sealed therapeutic shoe. The primary outcome is ulcer healing, secondary outcomes include (but are not limited to) skin complications, glycemic control, body mass index, gait function, balance, quality of life, physical activity, and health economics.

Full description

Data for the primary outcome of 112 participants are needed but the aim is to recruit 150, if possible within a reasonable time frame, to take drop-out into account.

Participants are randomized (blocked randomization, stratified for ulcer site and study center) to either treatment with a sealed therapeutic shoe or total contact cast.

Each participant will be assessed by a cast technician during the treatment period (for ulcer healing and skin complications) and be assessed by a physiotherapist on five occasions: at baseline, approximately 4 weeks into treatment and 1, 6 and 12 months after treatment end. On these occasions the physiotherapist will perform different tests (gait, balance, ankle strength and flexibility, bone mass density in heel bone, etc) and participants will answer questionnaires and have their physical activity measured for 7 days with an activity monitor.

Enrollment

4 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosed with diabetes mellitus (any kind)
  • Foot ulcer under metatarsal heads

Exclusion criteria

  • large ulcer (3-5 metatarsal heads)
  • critical ischemia (defined as toe pressure <30 mmHg or TcPO2 <30 mmHg)
  • uncontrolled infection (IWGDF infection grade 4, or grade 3 if not treatment against infection has been administered)
  • Active Charcot foot
  • foot deformities that necessitate custom-made shoes
  • inability to speak/read Swedish.
  • People with increased risk that side-effects will not be discovered or reported (dementia, abuse of alcohol or drugs, intellectual disability, etc.) if the person do not have appropriate social support, will be excluded.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

4 participants in 2 patient groups

Sealed shoe
Experimental group
Description:
Therapeutic footwear including off-the-shelf therapeutic shoes and custom-made insoles. The shoe on the ulcerated foot is "sealed", i.e., made irremovable, with a plastic band.
Treatment:
Device: Sealed therapeutic shoe
Total contact cast
Active Comparator group
Description:
A irremovable custom-made total Contact cast enclosing the foot and shin
Treatment:
Device: Total contact cast

Trial documents
2

Trial contacts and locations

3

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Central trial contact

Gustav Jarl, PhD

Data sourced from clinicaltrials.gov

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