Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Intervention1: Pre-peritoneal plus portal infiltration: 15 ml of 0.5% Ropivacaine will be instilled in pre-peritoneal space plus 5 ml of 0.5% Ropivacaine will be infiltrated in three portal sites. Tot
Sponsors
Sri Venkateshwaraa Medical College Hospital Research Centre
Eligibility
Inclusion criteria
Inclusion criteria: Patients of either sex in the age group of 18 to 60 years of American society of Anesthesiologists (ASA) physical status I or II.
Exclusion criteria
Exclusion criteria: Patients belonging to ASA3 and beyond Hypersensitivity to the study drug. Pregnant or lactating woman
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1.Duration of post- operative analgesia i.e. the time elapsed between the end of surgery and the first demand of analgesia by the patient. 2.The intensity of postoperative pain on visual analogue scale (VAS) for 24 hours postoperatively. Timepoint: 1.Demand for rescue analgesia 2.Fourth hourly for 24 hours. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1.The analgesia request rate in initial 24 hours postoperatively. 2.Incidence of seroma at the surgical site Timepoint: 1.First 24 hours 2.One month. | — |
Countries
India
Contacts
Public ContactRaghuraman MS
Sri Venkateshwaraa Medical College Hospital & Research Centre, Ariyur, Puducherry, INDIA.
Outcome results
None listed