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Corticosteroid injections in patients with trochanteric pain syndrome: open label randomized clinical trial in general practice.

Corticosteroid injections in patients with trochanteric pain syndrome: open label randomized clinical trial in general practice.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON20947
Enrollment
150
Registered
2006-03-27
Start date
2006-05-01
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Trochanteric pain, also known as trochanteric bursitis or pseudotrochanteric bursitis

Interventions

1. Intervention group: Usual care combined with corticosteroid injections (triamcenalonacetaat 40 mg, lidocaine 1%)
2. Control group: Usual care.

Sponsors

Erasmus Medical Center, Department of General Practice
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients aged 18 till 80 consulting the general practitioner with trochanteric hip pain existing longer then one week, with the following signs: 1. Severe local pain by pressure at the trochanter major, but unsure whether the patient recognizes this as the pain he/she consulted for; 2. Local pain by pressure at the trochanter major, which thepatient recognizes as the pain he/she consulted for.

Exclusion criteria

Exclusion criteria: 1. Patients who don’t understand the questionnaires because of inadequate mastering of Dutch language or cognitive disorders; 2. Patients who presented themselves in the previous year to the GP with the same complaints; 3. Patients with sensibility disorders due to meralgia paresthetica, patients who previously have undergone hip surgery at the same side and patients with systematic rheumatologic or neurologic disorders.

Design outcomes

Primary

MeasureTime frame
Experienced recovery (7 points Likert scale) and severity of pain (0-10 VAS) at 3 months follow up.

Secondary

MeasureTime frame
1. Disease specific outcomes of pain and function (WOMAC/HOOS), at 3 and 12 months follow up; 2. Primary outcomes at 6 weeks and at 6, 9 and 12 months follow-up; 3. Cost effectiveness over 12 months of follow-up. Costs will be estimated by medical consumption, and productivity loss (PRODISC).

Contacts

Public ContactS. Bierma-Zeinstra

Erasmus Medical Center, Department of General Practice, P.O. Box 1738

s.bierma-zeinstra@erasmusmc.nl+31 (0)10-4087633

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)