Analgesia Clinical Trial
Official title:
Comparative Study on Postoperative Analgesia With Transversus Abdominis Plane Block to Local Anesthetic Infiltration With Ropivacaine in Laparoscopic Abdominal Surgery
Verified date | August 2023 |
Source | National Academy of Medical Sciences, Nepal |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The goal of this clinical trial is to compare the postoperative analgesic efficacy of ultrasound-guided TAP block with Local Anesthetic Infiltration of ropivacaine in patients undergoing laparoscopic surgery. The main question it aims to answer is: • If Transversus Abdominis Plane block with Ropivacaine will produce long duration of analgesia than the Local Anesthetic Infiltration with ropivacaine after laparoscopic abdominal surgery .
Status | Completed |
Enrollment | 100 |
Est. completion date | February 25, 2023 |
Est. primary completion date | November 12, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 25 Years to 70 Years |
Eligibility | Inclusion Criteria: 1. Adult patients of either sex aged 25-70 years 2. ASA physical status I or II 3. Patient posted for elective abdominal laparoscopic surgery. Exclusion Criteria: 1. Any absolute contraindications to peripheral nerve blockade 2. History of Hypersensitivity to Drugs 3. Uncontrolled Diabetes Mellitus, Renal Failure, Hepatic failure 4. History of neuromuscular or psychiatric disease 5. Patient receiving psychotropic drug, chronic analgesic therapy 6. Pregnancy 7. Patient weight less than 50 kg |
Country | Name | City | State |
---|---|---|---|
Nepal | National Academy of Medical Sciences | Kathmandu | Bagmati |
Lead Sponsor | Collaborator |
---|---|
National Academy of Medical Sciences, Nepal |
Nepal,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Time to first rescue analgesia | The time of first complaint of pain by the patient. | Time Frame: upto first 24 hour after intervention | |
Other | Total pethidine consumption | At any point of time when VAS was>3, injection pethidine 0.5 mg/kg and injection promethazine 0.25 mg/kg was given via intravenous route | Time Frame: upto first 24 hour after intervention | |
Other | Total ketorolac consumption | When pain persisted for more than 15 min after giving intravenous pethidine, injection ketorolac 30 mg intravenous was given | Time Frame: upto first 24 hour after intervention | |
Primary | Duration of analgesia | Visual analog scale at rest | Time Frame: upto first 24 hour after intervention | |
Secondary | Duration of analgesia | Visual analog scale on movement | Time Frame: upto first 24 hour after intervention |
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