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Tape versus brace treatment of ankle distortion

Prospective randomized controlled trial comparing tape versus semi-rigid brace treatment of patients with grade II and III ankle ligament rupture

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN58932628
Enrollment
100
Registered
2011-07-28
Start date
2008-01-01
Completion date
Unknown
Last updated
2015-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ankle distortion, ankle ligament rupture Injury, Occupational Diseases, Poisoning Ankle sprain, ligament rupture

Interventions

1. Tape treatment: after randomisation tape immobilisation is started 5-8 days after initial treatment with immobilisation using bandage 2. Taping is performed by a select group of experienced and ski

Sponsors

Maastricht University Medical Center (Netherlabnds)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients were included if they sustained a grade II or III ankle sprain (significant damage to lateral ligaments defined by the presence of a lateral hematoma and tenderness at the anterior lateral ligament without or with instability) and were presented in the outpatient clinic within 5-7 days.

Exclusion criteria

Exclusion criteria: 1. Fracture 2. Age was under 16 or over 55 years 3. If they had experienced a previous ankle sprain or fracture 4. If they sustained swelling that makes tape treatment impossible

Design outcomes

Primary

MeasureTime frame
1. Patient satisfaction is assessed by verbal rating scale: poor (5), moderate (4), sufficient (3), good (2) and excellent (1) both at 2 and 4 weeks after start of the study treatment 2. Level of pain is evaluated using the visual analogue scale at baseline, 2, 4, 8 and 12 weeks 3. Ankle joint function is assessed using the validated Karlsson scoring scale at 2, 4, 8 and 12 weeks after start of the study treatment 4. Range of motion is measured using an electronic goniometer at 2, 4, 8 and 12 weeks after start of the study treatment

Secondary

MeasureTime frame
Any complications of the treatments

Countries

Netherlands

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026