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Clinical Trials/EUCTR2013-005106-64-AT
EUCTR2013-005106-64-AT
Active, not recruiting
Phase 1

Continous wound infiltration after hallux valgus surgery - CWI-HVS

Medizinische Universität Innsbruck0 sitesMarch 7, 2014
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ConditionsHallux valgus surgeryMedDRA version: 16.1Level: LLTClassification code 10019095Term: Hallux Valgus correctionSystem Organ Class: 100000004865Therapeutic area: Analytical, Diagnostic and Therapeutic Techniques and Equipment [E] - Anesthesia and Analgesia [E03]
DrugsRopinaest 2 mg/ml - Injektionslösung

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Hallux valgus surgery
Sponsor
Medizinische Universität Innsbruck
Status
Active, not recruiting
Last Updated
8 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 7, 2014
End Date
TBD
Last Updated
8 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • •All patients undergoing a distal metatarsal osteotomy (only Chevron or Scarf) and lateral release of the adductor hallucis muscle with/without concomitant osteotomy of the proximal phalanx of the greater toe (Akin) for idiopathic hallux valgus deformity will be included.
  • •Are the trial subjects under 18? no
  • •Number of subjects for this age range:
  • •F.1\.2 Adults (18\-64 years) yes
  • •F.1\.2\.1 Number of subjects for this age range 50
  • •F.1\.3 Elderly (\>\=65 years) no
  • •F.1\.3\.1 Number of subjects for this age range

Exclusion Criteria

  • •Exclusion criteria are 1\. hallux valgus surgery other then mentioned above or concomitant other procedures, 2\. denial to participate and give informed consent, 3\. patients with neurological diseases that affect the sensory\-motor function, 4\. patients with any short\-term (1 month) previous surgery on affected lower extremity, 5\. allergies or other comorbidity that prohibits standardized pain regime (renal insufficiency, severe heart or liver impairment, uncontrolled asthma, history of peptic ulcera ) or 6\. patients unwilling to undergo surgery without general anesthesia.

Outcomes

Primary Outcomes

Not specified

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