Health Condition 1: null- patients undergoing lower abdominal gynecological surgeries
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: ASA class I or II undergoing elective total abdominal hysterectomies
Exclusion criteria
Exclusion criteria: Contraindications to epidural anesthesia (coagulopathy, local infection),History of relevant drug allergy, Uncooperative patient, Patients with BMI > 35,History of chronic pain, History of previous surgery
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| to determine the effect of transversus abdominis plane block on the quality of postoperative analgesia as assessed using visual analogue scores (VAS) both at movement (coughing) and at restTimepoint: to determine the effect of transversus abdominis plane block on the quality of postoperative analgesia as assessed using visual analogue scores (VAS) both at movement (coughing) and at rest immediately in the post operative period and then at 30min, 1,2, 4,6,12,24,and 48hrs. | — |
Secondary
| Measure | Time frame |
|---|---|
| Bedside pulmonary function tests using Wrights respirometer Timepoint: 2, 4, 12, 24 hours;Total epidural local anaesthetic consumption in the 1st 48 hours postoperatively.Timepoint: upto 48 hrs | — |
Countries
India
Contacts
POST GRADUATE INSTITUTE OF MEDICAL EDUCATION AND RESEARCH, CHANDIGARH, INDIA