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comparative between butorphanol and nalbuphine as to adjuvants to spinal bupivacaine in infra umbilical surgeries

Not Applicable
Not yet recruiting
Conditions
Health Condition 1: K409- Unilateral inguinal hernia, without obstruction or gangrene
Registration Number
CTRI/2019/04/018408
Lead Sponsor
Yawanth Reddy
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Not Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Patients posted for lower abdominal, lower limb surgeries under spinal anaesthesia

Exclusion Criteria

Patients allergic to local anaesthetics, nalbuphine/ Butorphanol

ASA physical status III or more

Height <140cms and BMI >30 kg/m2

Patient contraindicated for spinal anaesthesia

Patient who had acute and chronic pain elements

Patient refusal

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To compare the duration of analgesia in terms of time to first analgesic requirement. <br/ ><br>Timepoint: Postoperatively <br/ ><br>
Secondary Outcome Measures
NameTimeMethod
To compare quality of analgesia measured in terms of total analgesic requirement . <br/ ><br> <br/ ><br>To compare pain scores, duration of motor blockade, perioperative hemodynamic parameters. <br/ ><br> <br/ ><br>To study the incidence of opioid related side effects in the two groups <br/ ><br>Timepoint: intra operatively and Postoperatively
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