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The effect of postoperative physiotherapy, after Chevron osteotomy, on foot function. A randomized controlled trial.

The effect of postoperative physiotherapy, after Chevron osteotomy, on foot function. A randomized controlled trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON28807
Enrollment
60
Registered
2011-07-06
Start date
2011-09-01
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

Hallux valgus Surgical correction Chevron osteotomy Physiotherapy Outcome Foot function

Interventions

Postoperative physiotherapy, after surgical correction of a hallux valgus deformity, by a Chevron osteotomy. Two groups of patients will be compared. Both groups will be operated, with surgical corre

Sponsors

Isala Klinieken, Zwolle, The Netherlands
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients with an indication for Chevron osteotomy: Intractable pain isolated to the first or second MTP joint region, associated with a hallux valgus deformity, refractory to conservative treatment (shoe modifications, NSAIDs, modification of activities), with following rontgenographic details: Intermetatarsal Angle ≤ 20o; 2. Age 18-65; 3. Physiologic preoperative gait pattern.

Exclusion criteria

Exclusion criteria: Specific comorbidity: Inflammatory arthritis, degenerative arthritis of the first MTP joint, previous foot surgery, rheumatoid arthritis, diabetes mellitus, peripheral vascular disease, neuropathy, neuromuscular disease, active infection, incompetent person.

Design outcomes

Primary

MeasureTime frame
AOFAS Hallux score.

Secondary

MeasureTime frame
1. Function of first MTP-joint: This will be measured by placing a hand-held goniometer parallel to the long axis of the first metatarsal and the hallux; 2. Foot Function Index25; 3. VAS pain/satisfaction/ cosmesis.

Contacts

Public ContactJ.C.M. Schrier
+31 (0)6 18515625

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)