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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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12 December 2020 |
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Main ID: |
NCT02330302 |
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Date of registration:
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31/12/2014 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Single Shot Fascia Iliaca Block vs Femoral Nerve Block for Analgesia for Surgical Fixation of Hip Fractures
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Scientific title:
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A Randomized Controlled Trial Comparing Single Shot Fascia Iliaca Block With Femoral Nerve Block for Analgesia Following Surgical Fixation of Hip Fractures |
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Date of first enrolment:
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August 2014 |
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Target sample size:
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30 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT02330302 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: Double (Participant, Outcomes Assessor).
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Phase:
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N/A
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Countries of recruitment
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Singapore
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Contacts
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Name:
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Yean Chin Lim, MBBS, MMed |
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Address:
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Telephone:
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Email:
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Affiliation:
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Changi General Hospital |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Patients scheduled for surgical fixation of hip fracture
- Patients with isolated inter-trochantric fracture
- American Society of Anesthesiologists (ASA) physical status 1 to 3
- Patients who are able to give their own consent
Exclusion Criteria:
- Patients unable to give consent or inability to communicate/ cooperate
- Patients with regular consumption of strong opioids (morphine, oxycodone) or steroids
- Patients with allergy to local anaesthetics or any drugs included in the study
- Patients with contraindications to spinal anaesthesia such as coagulation disorders/
thrombocytopenia and local infection at site of injection
Age minimum:
N/A
Age maximum:
N/A
Gender:
All
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Health Condition(s) or Problem(s) studied
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Hip Fracture
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Intervention(s)
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Drug: Ropivacaine
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Primary Outcome(s)
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Pain scores
[Time Frame: up to 24 hours]
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Secondary Outcome(s)
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opioid requirement/consumption
[Time Frame: for first 24 hrs (including intra operatively) following intervention]
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Secondary ID(s)
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2014/453/D
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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