Health Condition 1: null- breast cancer
Conditions
Interventions
Intervention1: epidural injection of ropivacaine alone versus butorphanol or fentanyl as adjuvant to ropivacaine: To compare postoperative pain relief using epidural ropivacaine,
ropivacaine-butorphan
Group B will receive 6ml of 0.25% ropivacaine with
butorphanol 1ml (1mg/ml) and 1 ml normal saline through epidural
route.
Group C will receive 6ml of 0.25% ropivacaine with 2 ml fentanyl (100
micrograms) through epidural route. The post operative analgesia will be
given as epidural top ups in the form of ropivacaine(0.12
Sponsors
Sri Guru Ram Das Institute Of Medical Sciences And Research
Eligibility
Inclusion criteria
Inclusion criteria: ASA grade 1 & 2
Exclusion criteria
Exclusion criteria: 1. Patients having bleeding diathesis 2. Patients on any anticoagulant therapy 3. Patients with known hypersensitivity to local anaesthetics or study drugs. 4. Patients having history of drug abuse 5. Patients who are mentally retarded 6. Patient suffering from uncontrolled asthma, cardiac, respiratory, renal, thyroid, hepatic and CNS disorders. 7. Patients with local sepsis or spinal deformity.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Duration Of Postoperative AnalgesiaTimepoint: Duration Of Analgesia From Drug Administration To VAS Equals To Or More Than 4 in Postoperative Period In First 24 Hours | — |
Secondary
| Measure | Time frame |
|---|---|
| 1.Intraoperative Haemodyanamic Stability 2.Total Dose Of Postoperative Analgesic RequirementTimepoint: 1. Intraoperative Haemodyanamical Stability Upto End of Surgery 2. In First 24 Hours | — |
Countries
India
Contacts
Public ContactDr Ishpuneet singh
Sri Guru Ram Das Institute Of Medical Sciences And Research
Outcome results
None listed