To study the effect of Epidural Volume Extension with saline in Combined Spinal Epidural in low dose spinal anaesthesia.
Phase 4
- Conditions
- Health Condition 1: S720- Fracture of head and neck of femurHealth Condition 2: O- Medical and Surgical
- Registration Number
- CTRI/2023/06/053959
- Lead Sponsor
- Dr Rajendra Prasad Government Medical College Kangra
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.ASA class I-III
2.BMI between 18.5-29.9.
Exclusion Criteria
1.Patientâ??s refusal to participate in the
study.
2.Patients with severe anatomical spinal
deformities.
3.Patients with bleeding disorders
4.Patients with local infection at the sites
where needle for CSE is to be inserted.
5.Patients with dysarrhythmias.
6.Patients allergic to study drug.
7.Patients on anticoagulants.
8.Failure of spinal/epidural anesthesia.
9.Anticipated duration of surgery more than
2 hour duration.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Maximum level of sensory block attainedTimepoint: Every minute until the highest level is stabilised.
- Secondary Outcome Measures
Name Time Method Characteristics of motor & sensory block, hemodynamic changes, adverse events & additional analgesic requirements upto 24 hrs.Timepoint: Hemodynamics measurement at 0, 3, 6, 9,12,15,18,21,24,27,30,35,40,45,50,55,60,65,70,75,80,85,90,95,100,105,110,115,120 minutes. <br/ ><br>Number of rescue analgesia given in 24 hrs. <br/ ><br>