Health Condition 1: C509- Malignant neoplasm of breast of unspecified site
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Adult female patients aged =18 year who will undergo elective MRM surgery at the RIMS, RANCHI and who met the criteria of classes I–III of the American Society of Anesthesiology (ASA) classification will be eligible for inclusion in the study
Exclusion criteria
Exclusion criteria: Age criteria. Also, patients who would unconscious or mentally incompetent prior to surgery, or who would in ASA classes IV or V, or had coagulopathy or hemodynamic instability (systolic blood pressure allergic reactions to opiates or to local anesthetic agents wil be excluded from the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Assessment of the level of post-operative pain (on NRS scores) Timepoint: Post-operative pain on NRS score at post-op 0,1,2,4,12 and 24 hours. | — |
Secondary
| Measure | Time frame |
|---|---|
| (1) Time needed to the first rescue analgesic in minutes. (2) Cumulative dose of rescue analgesic needed (cumulative dose of tramadol & fentanyl). (3)Rate of patient satisfaction (on a 1 to 10 scale). (4)The incidence of nausea & any attack of post-operative vomiting (5)The incidence of any of the serratus anterior plane blocks complications e.g. injection site hematoma or signs or symptoms of local anesthetic toxicity. Timepoint: post-op period upto patient discharge. | — |
Countries
India
Contacts
RIMS, RANCHI