Comparison of effect on pain relief between Programmed Intermittent Bolus and Continuous Infusion of drugs in ultrasound guided nerve block in upper limb surgery.
- Conditions
- Health Condition 1: M849- Disorder of continuity of bone, unspecified
- Registration Number
- CTRI/2020/03/023830
- Lead Sponsor
- Government Medical College and Hospital Chandigarh
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 30
American Society of Anesthesiologists (ASA) physical status I-II, Age 18-65 years, BMI – 18-30 kg/m2,Either of the genders, Undergoing upper limb surgery distal to mid-humerus.
1. Patient refusing to give informed consent
2. History of relevant drug allergy
3. History of psychiatric illness, substance abuse
4. Severe cardiovascular, respiratory, metabolic or neurological disease
5. Pregnancy and lactation
6. Coagulopathy
7. Contralateral phrenic nerve dysfunction
8. Infection at planned injection site
9. Patients on steroids
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Total 48-h consumption of local anaesthetic-opioid mixture (in ml) by patient controlled regional analgesiaTimepoint: 48 hours
- Secondary Outcome Measures
Name Time Method 1. Pain assessment using 11-point (0-10) numerical rating scale (NRS) over 48h study period at time intervals of 1, 4, 12, 24, 36 and 48h <br/ ><br>2. Sensory and motor blockade <br/ ><br>3. Patient satisfaction <br/ ><br>4. Adverse effectsTimepoint: 48 hours
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