study of the effects of two forms of epidural bupivacaine on postoperative pain following total knee replacement
Not Applicable
Completed
- Conditions
- Surgerypostoperative pain
- Registration Number
- PACTR201502001010803
- Lead Sponsor
- menoufiya university
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
ASA 2 and 3 patients
who will undergo one side total knee replacement
age from 50 to 80 , both male and female
Exclusion Criteria
ASA 4 patients
patients who are receiving anti platelets till the operation day.
patients with coagulopathies
patients with sever back deformities or infection at the planned site of epidural
hemodynamically unstable patients with poor systolic function.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms explain bupivacaine's analgesic effects in postoperative pain management?
How does epidural bupivacaine compare to standard-of-care analgesics for total knee replacement recovery?
Are there specific biomarkers that predict patient response to epidural bupivacaine formulations?
What adverse events are associated with epidural bupivacaine administration in orthopedic surgery?
What combination therapies enhance bupivacaine efficacy in managing postoperative knee pain?