A study testing the two ways of using the pain relief injection in breast surgery to see if both the ways work similar to one another.

INTERVENTION: Intervention1: GROUP S Superficial serratus posterior superior intercostal block: Patients in Group S will receive a superficial SPSIB, in which the drug is administered in the plane between Serratus posterior superior muscle and Rhomboid major muscle Control Intervention1: GROUP D Deep serratus posterior superior intercostal block: Patients in Group D will receive a deep SPSIB, in which the drug is administered in the plane between serratus posterior superior muscle and the third rib. CONDITION: Health Condition 1: C509‐ Malignant neoplasm of breast of unspecified site Health Condition 2: O‐ Medical and Surgical PRIMARY OUTCOME: Dynamic Numeric rating‐ Pain score ; ; Timepoint: At 24 hours ; ; SECONDARY OUTCOME: Area under curve of NRS‐Pain score in 24 hoursTimepoint: at 24 hours after surgery Dermatomal assessmentTimepoint: 2 hours after extubation NRS‐Pain scores at rest and dynamic ; Timepoint: 0, 1, 2, 3, 4, 6, 12 and 24 hours after surgery ; Postoperative nausea vomiting scoreTimepoint: 0, 1, 2, 3, 4, 6, 12 and 24 hours after surgery Quality of Recovery 15 scoreTimepoint: at baseline and then at the end of day 1. Satisfaction scoreTimepoint: at 24 hours Time to first request of analgesicTimepoint: within 24hours following surgery Total consumption of rescue analgesic in 24 hoursTimepoint: within 24 hours following surgery INCLUSION CRITERIA: Consenting female patients with body mass inde Xof 18 to 35 kg per meter square, age 18years to 65 years with American Society of Anesthesiologists physical status I to III undergoing elective unilateral modified radical mastectomy with axillary node clearance under general anesthesia