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Effect of Two drugs infusion for postoperative analgesia in patients undergoing upper abdominal surgeries

Not Applicable
Conditions
Health Condition 1: K928- Other specified diseases of the digestive system
Registration Number
CTRI/2022/07/043764
Lead Sponsor
Department of Anaesthesiology
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

Patient of either gender of age between 18-65 years undergoing major upper abdominal cancer surgery and classified as American Society of Anesthesiologists (ASA) physical status class Iâ??III.

Exclusion Criteria

Age less than 18 year or more than 65 year.

Patients with treatment of α-adrenergic antagonists

History of arrhythmias, contraindications to placement of an epidural catheter (eg,

coagulopathy, local infection, and vertebral anomalies), patients known to be allergic to bupivacaine, dexmedetomidine, or morphine, and patients treated with regular chronic pain medications.

Non willing patents.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To compare the postoperative pain using VAS score during rest and movement at <br/ ><br>different time postoperativelyTimepoint: 4 weeks
Secondary Outcome Measures
NameTimeMethod
To assess rescue analgesia, sedation score, intraoperative and postoperative <br/ ><br>hemodynamics, bowel recovery time, nausea and vomitingTimepoint: 48 hours
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