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Postoperative Analgesia With Local Infiltration After Hip Fracture
This study is currently recruiting participants.
Verified by Odense University Hospital, December 2008
Sponsored by: Odense University Hospital
Information provided by: Odense University Hospital
ClinicalTrials.gov Identifier: NCT00529425
  Purpose

Reducing pain is an essential factor for early mobilization after internal fixation of hip fractures. Systemic opioids have side effects that might obstruct mobilization and induce delirium and nausea. The investigators hypothesized that wound infiltration results in reduction in systemic opioid usage and pain relief without side effects.


Condition Intervention Phase
Hip Fracture
Drug: Ropivacaine
Phase IV

MedlinePlus related topics: Fractures Hip Injuries and Disorders Hip Replacement
Drug Information available for: Ropivacaine Ropivacaine Hydrochloride Ropivacaine monohydrochloride
U.S. FDA Resources
Study Type: Interventional
Study Design: Randomized, Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Parallel Assignment, Efficacy Study
Official Title: Postoperative Analgesia With Local Infiltration After Hip Fracture vs. Traditional Treatment of Pain With Opioids

Further study details as provided by Odense University Hospital:

Estimated Enrollment: 100
Study Start Date: February 2008
  Eligibility

Genders Eligible for Study:   Both
Criteria

Inclusion Criteria:

  • Pertrochanteric fractures
  • Femoral neck fractures
  • Only inclusion of one fracture per patient
  • Low-energy trauma
  • Ability to understand danish and give informed consent
  • Ability to walk

Exclusion Criteria:

  • Refusal to participate
  • Substance abuse
  • Drug intolerance
  • Pathological fractures
  • Inverse fractures
  • Intraarticular inflammation
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00529425

Contacts
Contact: Rune Dueholm Bech, MD +45 6611 3333 ext 4668 rune.bech@dadlnet.dk

Locations
Denmark
Odense University Hospital Recruiting
Odense, Denmark, 5000
Contact: Rune D. Bech, MD     +45 6611 3333 ext 4668     rune.bech@dadlnet.dk    
Sponsors and Collaborators
Odense University Hospital
Investigators
Study Chair: Soeren Overgaard, Professor, MD, DmSc Odense University Hospital, DK-5000 Odense C, Denmark
  More Information

Study ID Numbers: S-VF-20060072
Study First Received: September 12, 2007
Last Updated: December 29, 2008
ClinicalTrials.gov Identifier: NCT00529425  
Health Authority: Denmark: Danish Dataprotection Agency

Study placed in the following topic categories:
Hip Fractures
Femoral Fractures
Ropivacaine
Fractures, Bone
Wounds and Injuries
Disorders of Environmental Origin
Leg Injuries
Pain

Additional relevant MeSH terms:
Sensory System Agents
Therapeutic Uses
Physiological Effects of Drugs
Central Nervous System Depressants
Anesthetics
Peripheral Nervous System Agents
Hip Injuries
Central Nervous System Agents
Pharmacologic Actions
Anesthetics, Local

ClinicalTrials.gov processed this record on January 15, 2009