Health Condition 1: C50- Malignant neoplasm of breast
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Inclusion criteria: a. Adult female patients planned for MRM b. Willingness to participate
Exclusion criteria
Exclusion criteria: Patients with known allergy to local anaesthetic drugs, patients posted for bilateral MRM in the same sitting, or for pedicle flap or implant reconstruction along with breast oncosurgeries
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the postoperative analgesic outcome between Drain Block, SIFB and Parenteral ParacetamolTimepoint: 1 year duration | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. To compare the ease of administration of postoperative analgesia between different groups 2. To determine the requirement of rescue analgesics between different groupsTimepoint: Postoperatively | — |
Countries
India
Contacts
Chittaranjan National Cancer Institute