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Clinical Trial Summary

Falls are a common problem in elderly patients resulting fractured femur, which require early operation. Adequate postoperative pain control will provide good recovery. The investigators will compare the efficacy of postoperative pain control among intrathecal morphine, femoral nerve block, and periarticular infiltration with bupivacaine in patients undergone intramedullary hip screw under spinal anesthesia.


Clinical Trial Description

Study methods :

Every patients without any exclusion criteria will be performed spinal anesthesia by 0.5% heavy bupivacaine then divided into 4 groups

1. Controlled group : spinal anesthesia alone

2. Femoral nerve block by 20 mL of 0.25% bupivacaine before spinal anesthesia

3. Spinal anesthesia plus 0.1 mg morphine intrathecally

4. Spinal anesthesia plus periarticular infiltration with 20 mL of 0.25% bupivacaine

All patients will receive postoperative intravenous patient controlled analgesia (IV PCA) morphine for 48 hours.

Data collection

1. Demographic data

2. Pain score : preoperative, 3 hours postoperative in the 1st six hours, 12 hours postoperative by visual analog scoring system (VASS)

3. Patient global assessment and patient satisfactory VASS at 24 and 48 hours postoperative

4. The amount of morphine at 24 and 48 hours postoperative and the time of the 1st dose ;


Study Design

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


Related Conditions & MeSH terms


NCT number NCT01219088
Study type Interventional
Source Mahidol University
Contact Thitima Chinachoti, M.D.
Phone 66813082438
Email sitci35@gmail.com
Status Recruiting
Phase Phase 4
Start date September 2010
Completion date September 2012

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