Health Condition 1: Z488- Encounter for other specified postprocedural aftercare Health Condition 2: O- Medical and Surgical
Conditions
Interventions
Intervention1: Administration of either tramadol or bupivacaine: Prophylactic wound infiltration with either tramadol or bupivacaine. Inj.Tramadol hydrochloride 2 mg/kg in 20 mL of 0.9% normal saline,
Sponsors
Maharaja Agrasen Medical College, Agroha
Eligibility
Inclusion criteria
Inclusion criteria: 1. American Society of Anaesthesiologistsâ?? physical status II. 2. Patients undergoing caesarean section under subarachnoid block.
Exclusion criteria
Exclusion criteria: Patients 1. who refuse to give consent 2. with severe cardiopulmonary, renal or liver disease, pre-eclampsia, eclampsia, seizure disorder. 3. with contraindication to spinal anaesthesia like local site infections, coagulopathies or any spinal deformities. 4. who have infection at surgical site. 5. with history of allergy or hypersensitivity to local anaesthetics 6. with psychiatric illness that would interfere with assessment of pain will be excluded from the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Comparison between the analgesic efficacy of wound infiltration with tramadol and bupivacaine for postoperative pain using NRS and time of rescue analgesia.Timepoint: Assessment of post operative pain and time of rescue analgesia for upto 24 hours. | — |
Secondary
| Measure | Time frame |
|---|---|
| Incidence of adverse events.Timepoint: 24 hours post operative. | — |
Countries
India
Contacts
Public ContactRUCHIKA KATHURIA
Maharaja Agrasen Medical College, Agroha, Hisar
Outcome results
None listed