Comparison between epidural mode of pain relief and multimodal pain relief(given perioperatively)in lower abdominal surgeries
Phase 3
Not yet recruiting
- Conditions
- Health Condition 1: K45- Other abdominal hernia
- Registration Number
- CTRI/2021/02/031401
- Lead Sponsor
- il
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA GRADE I & II
AGED BETWEEN 20-70 YEARS
PATIENTS UNDERGOING LOWER ABDOMINALSURGERIES UNDER GENERAL ANAESTHESIA
Exclusion Criteria
PATIENT NOT GIVING CONSENT
HISTORY OF DRUG ABUSE
PREGNANCY
ASA GRADE III &IV
HISTORY OF SEIZURES
PREEXISTING CHRONIC OR ACUTE PAIN OR PREVIOUS ABDOMINAL SURGERIES IN LAST 3 MONTHS
PATIENT WITH KNOWN HYPERSENSITIVITY TO ANY OF THE STUDY DRUG
PATIENT WITH SIGNIFICANT CARDIOVASCULAR HEPATIC PULMONARY RENAL HEMATOLOGICAL NEUROLOGICAL OR PSYCHIATRIC ILLNESS.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method TO INCORPORATE MULTIMODAL ANALGESIA INCLUDING PERIOPERATIVE ANTINOCICEPTION INTO THE ANALGESIC REGIMEN OF PATIENTS UNDERGOING LOWER ABDOMINAL SURGERIES.Timepoint: 1 year
- Secondary Outcome Measures
Name Time Method TO EVALUATE AND COMPARE THE EFFECT OF MULTIMODAL ANALGESIA AND EPIDURAL ANALGESIA ON EARLY AMBULATION OF PATIENT UNDERGOING LOWER ABDOMINAL SURGERIES.Timepoint: 1 YEAR