TO FIND OUT THE EFFECT OF CLONIDINE USED ALONGWITH 0.5% BUPIVACAINE IN ESP BLOCK FOR BREAST SURGERIES WHICH IS A TYPE OF RANDOMIZED CONTROLLED TRIA
Not Applicable
Not yet recruiting
- Conditions
- Health Condition 1: C50- Malignant neoplasm of breast
- Registration Number
- CTRI/2021/09/036793
- Lead Sponsor
- AIIMS JODHPUR
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
PATIENTS WITH ASA PHYSICAL STATUS 1 AND/OR 2 AND UNDERGOING UNILATERAL MODIFIED RADICAL MASTECTOMY WILL BE INCLUDED IN THE STUDY
Exclusion Criteria
PATIENTS REFUSAL,PREGNANT PATIENTS,PATIENTS WITH BASELINE COGNITIVE DEFICITS,COAGULOPATHY,LIVER AND RENAL DYSFUNCTION,KNOWN ALLERGY TO AMIDE LOCAL ANAESTHETICS OR OPIOID WILL BE EXCLUDED
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method TO DETERMINE THE EFFICACY OF USING CLONIDINE AS AN ADJUVANT IN ERECTOR SPINAE PLANE BLOCK IN TERMS OF DURATION OF ANALGESIA DEFINED AS TIME FROM ESP BLOCK TO FIRST RESCUE ANALGESIC,PATIENT DEMAND OR VAS GREATER THAN 4,AFTER BREAST SURGERIESTimepoint: VAS SCORE WILL BE RECORDED EVERY 30 MINS TILL 2 HRS IN PACU AND THEN AT 2,4,6,8,12TH HOUR TILL 24HOURS IN THE WARD
- Secondary Outcome Measures
Name Time Method ADVERSE EFFECTS/COMPLICATIONS IF ANYTimepoint: FROM ESP BLOCK TO 24 HOUR POSTOPERATIVELY;DURATION OF SENSORY BLOCKTimepoint: FROM ESP BLOCK TO ONSET OF PAIN;NUMBER OF DERMATOMES BLOCKEDTimepoint: BLOCK COMPLETION TO GRADE 1 SENSORY BLOCK;ONSET OF SENSORY BLOCKTimepoint: BLOCK COMPLETION TO GRADE 1 SENSORY BLOCK;QUALITY OF ANALGESIA BY VISUAL ANALOGUE SCALETimepoint: FROM ESP BLOCK TO FIRST RESCUE ANALGESIC;TOTAL ANALGESIC REQUIREMENTTimepoint: 24 HOUR POSTOPERATIVELY