Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Intervention1: Diclofenac sodium 100 mg rectal suppository for postoperative analgesia: Arm A Diclofenac Suppository
Intervention: Diclofenac sodium rectal suppository
Dose: 100 mg
Route of admini
Sponsors
SRM Institute of Science And Technology
Eligibility
Inclusion criteria
Inclusion criteria: 1.Patients age group between 35to 70 years 2.Patients with ASA I, II & III 3.Patients having BMI of less than or equal to 40 kg/m 4.Patients who scheduled for elective abdominal hysterectomy under spinal anesthesia. 5.Expected to stay in the hospital for at least 24 h after surgery
Exclusion criteria
Exclusion criteria: 1.Patients with impaired cognitive function or psychiatric disorders 2.Patients who decline participation or withdraw consent 3.Patients with history of chronic pain 4.Patients with history of allergy to local anaesthetics or NSAIDs. 5.Patients with coagulopathy and cardiovascular disease. 6.Patients with history of kidney disease.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The findings from this research will provide valuable evidence to guide clinical decision making in postoperative pain management, potentially improving patient outcomes, satisfaction and quality of care.Timepoint: 1.Patients will be assessed for their baseline pain level using the Visual Analog Scale (VAS) during preanesthetic visit. 2.Intervention administration: At end of surgery / 1 hour before end of surgery (patch) 3.Postoperative pain assessment: Every 2 hours for 24 hours | — |
Secondary
| Measure | Time frame |
|---|---|
| Rescue analgesic requirement, time to first rescue analgesia, patient satisfaction score, and incidence of adverse effects assessed during the first 24 postoperative hours.Timepoint: Every 2 hours for first 24-hour postoperative period | — |
Countries
India
Contacts
Public ContactRanjith Kumar J
SRM Institute of Science and Technology
Outcome results
None listed