Ultrasound guided Erector spinae plane block with Versus without Clonidine for perioperative breast analgesia.
Not yet recruiting
- Conditions
- Malignant neoplasm of central portion of breast,
- Registration Number
- CTRI/2020/12/029557
- Lead Sponsor
- pgimer
- Brief Summary
This study will assess the significance of adding clonidine to the anesthetic mixture for women undergoing breast surgery under ESPB in terms of opioid and other analgesic consumption. secondary objectives were to assess pain scores, perioperative hemodynamic stability , return to daily activity.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- Female
- Target Recruitment
- 60
Inclusion Criteria
- ASA grade I-II healthy Adults 2.
- Patients above the age of 18 years to 65 years 3.
- Patients who can understand the VAS scale.
Exclusion Criteria
- Patient refusal to participate 2.
- Patient unable to co-operate 3.
- Local sepsis at the site of block 4.
- Coagulability/ patient on anti-coagulants 5.
- Known hypersensitivity to local anaesthetics or morphine.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The duration of opioid free analgesia of Erector Spinae Plane Block with local anesthetic alone versus local anesthetic mixture with added clonidine for perioperative pain relief in patients undergoing Breast surgeries 00 hours, 02 hours, 06 hours, 12 hours, 24 hours
- Secondary Outcome Measures
Name Time Method 1.To compare the total rescue opioid or opioid equivalent drugs required in the first 24 hours after surgery. 2.To compare the complications associated with the this regional anaesthetic technique.
Trial Locations
- Locations (1)
nehru hospital, ot complex, 4th floor, general surgery ot
🇮🇳Chandigarh, CHANDIGARH, India
nehru hospital, ot complex, 4th floor, general surgery ot🇮🇳Chandigarh, CHANDIGARH, Indiadr kulbhushan sainiPrincipal investigator9968856948kulbhushansaini007@gmail.com