None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: â?? ASA grade I or II patients â?? Undergoing abdominal surgeries under GA/SAB â?? Patients aged 18 to 60 years, of either sex
Exclusion criteria
Exclusion criteria: 1. Patients with a history of cardiac, respiratory, renal or hepatic disease. 2. Local infection at the site of block. 3. Psychological disorders, 4. Allergy to study medications. 5. coagulation disorders.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome of the study will be visibility of the block needle at the time of reaching the TAP plane according to the blinded observers 20 -30minutesTimepoint: The primary outcome of the study will be visibility of the block needle at the time of reaching the TAP plane according to the blinded observers | — |
Secondary
| Measure | Time frame |
|---|---|
| 5. number of skin punctures made; 6. number of catheter reinsertions required; 7. block success rate (as judged byVAS scores); 8. incidence of vascular puncture. Timepoint: 24 hrs | — |
Countries
India
Contacts
KING GEORGE MEDICAL UNIVERSITY LUCKNOW