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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00529425
Other study ID # S-VF-20060072 - femoral neck
Secondary ID
Status Completed
Phase Phase 4
First received September 12, 2007
Last updated May 5, 2010
Start date January 2008
Est. completion date December 2008

Study information

Verified date April 2010
Source Odense University Hospital
Contact n/a
Is FDA regulated No
Health authority Denmark: Danish Medicines Agency
Study type Interventional

Clinical Trial Summary

Reducing pain is an essential factor for early mobilization after osteosynthesis of femoral neck 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.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date December 2008
Est. primary completion date
Accepts healthy volunteers
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Femoral neck fracture

- Fracture due to low energy trauma

- Ability to understand danish and give informed consent

- Ability to walk before trauma

- Indication for osteosynthesis

- = 8 in OMC (Orientation-Memory-Concentration) test with a possible maximum of 28 points

- Informed consent

Exclusion Criteria:

- Drug or medical abuse

- Drug intolerance

- Pathological fractures

- Inflammatory arthritis

- Patient included in the study with the contralateral hip

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Intervention

Drug:
Ropivacaine


Locations

Country Name City State
Denmark Odense University Hospital Odense

Sponsors (1)

Lead Sponsor Collaborator
Odense University Hospital

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Consumption of opioids
Secondary Pain
See also
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Active, not recruiting NCT02362971 - External Validity of a Randomized Trial in Patients With a Femoral Neck Fracture N/A
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Completed NCT01052974 - Perioperative Analgesia by Femoral Perineural Catheter for Femoral Neck Fracture - Study KTcol Phase 4
Terminated NCT02030431 - Dynaloc for Treatment of Femoral Neck Fractures N/A
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Completed NCT02512094 - Validity and Reliability of Thai Version of Barthel Index for Hip Fracture Patients N/A
Recruiting NCT02148848 - Short-term Functional Recovery Between Early- and Late Bisphosphonate Treatment Following Hemiarthroplasty Phase 4
Completed NCT01644227 - Dual Mobility Cup in Total Hip Arthroplasty Preventing Dislocation in Patients at Risk N/A
Active, not recruiting NCT02901938 - Feasibility of Implantation of Cemented Femoral Stem for Osteoporotic Femoral Neck Fracture in Elderly Patients N/A