Post Surgical Pain Clinical Trial
Official title:
An Ultrasound Guided Fascia Iliaca Block Placed at the Level of the Inguinal Ligament for Analgesia After Hip Arthroplasty
Verified date | March 2018 |
Source | McMaster University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Hip replacement surgery is one of the most common elective surgeries in Canada and with this surgery, there is considerable pain after the operation. By decreasing the amount of pain after surgery, the patients may be able to move and walk quicker, resulting in easier physiotherapy sessions, shorter hospital stays and may help to avoid adverse outcomes like nausea and vomiting and being overly sedated. By using ultrasound guided femoral nerve block, it may be an alternative for pain management with minimal side effects for patients having hip replacement surgery.
Status | Completed |
Enrollment | 24 |
Est. completion date | August 2017 |
Est. primary completion date | August 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 85 Years |
Eligibility |
Inclusion Criteria: 1. Patients 18 years or older undergoing unilateral hip arthroplasty. 2. Patient capable to complete informed consent. Exclusion Criteria: 1. Pediatric population. 2. Inability to complete informed consent. 3. Patient refusal. 4. Contraindication for regional anesthesia: coagulopathy, anticoagulant use, bleeding disorders, local or systemic infection, local anesthesia allergy. 5. Presence of neuromuscular deficit including diabetic peripheral neuropathy. |
Country | Name | City | State |
---|---|---|---|
Canada | St. Joseph's Heathcare Hamilton | Hamilton | Ontario |
Lead Sponsor | Collaborator |
---|---|
McMaster University | St. Joseph's Healthcare Hamilton |
Canada,
Rothwell MP, Pearson D, Hunter JD, Mitchell PA, Graham-Woollard T, Goodwin L, Dunn G. Oral oxycodone offers equivalent analgesia to intravenous patient-controlled analgesia after total hip replacement: a randomized, single-centre, non-blinded, non-inferiority study. Br J Anaesth. 2011 Jun;106(6):865-72. doi: 10.1093/bja/aer084. Epub 2011 Apr 13. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The primary outcome is number of patients recruited per week and we hope to recruit 2 patients per week. | Three months | ||
Secondary | Number of eligible patients consenting to participate. | Three months | ||
Secondary | Number of patients participating that were randomized and received the study intervention. | Three months | ||
Secondary | Completion of study data collection forms | Three months | ||
Secondary | Incidence of respiratory depression and seizures in participating subjects | Three months |
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