Pain, Postoperative Clinical Trial
— TAPAOfficial title:
TAPA Block Versus Conventional Analgesia Methods on Cognitive Functions and Postoperative Opioid Consumption in Major Abdominal Surgery
Verified date | March 2023 |
Source | Dr Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
It was planned to compare the opioid consumption and cognitive functions in the postoperative period of patients who received TAPA block for postoperative analgesia and patients who did not prefer the block and who preferred intravenous patient-controlled analgesia (PCA) with opioids. Both the surgery applied and the drugs used in anesthesia can cause changes in cognitive functions by affecting the inflammatory process. It is thought that if the patients' pain can be relieved sufficiently in the postoperative period with TAPA block, the consumption of opioids used will be less and their cognitive functions will be less affected.
Status | Completed |
Enrollment | 90 |
Est. completion date | September 10, 2022 |
Est. primary completion date | August 20, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 85 Years |
Eligibility | Inclusion Criteria: 1. patients who will undergo major abdominoplasty, 2. over the age of 18, 3. under the age of 85, 4. patients who has ASA (American Society of Anesthesiologists) II and ASA III criteria Exclusion Criteria: 1. younger than 18 years old, over 85 years old, 2. Having a history of cerebrovascular disease 3. Having surgery other than oncological surgery 4. having coagulation disorder 5. being illiterate 6. having visual and auditory problems 7. Inability to cooperate with cognitive function test 8. having an emergency surgery 9. Those who are not able to read and sign the consent form 10. Patients deemed unsuitable by the researcher 11. Patients who do not want to participate |
Country | Name | City | State |
---|---|---|---|
Turkey | SBU Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital | Ankara |
Lead Sponsor | Collaborator |
---|---|
Dr Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital |
Turkey,
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Cognitive functions | Cognitive functions will be evaluated with Mini-mental test in each patient on postoperative day 3. | postoperative day 3 | |
Secondary | postoperative pain scores | Postoperative pain scores will be recorded. The evaluation will be made with Visual Analogue Scale (VAS) score in the 1st, 2nd, 6th, 12th and 24th hours postoperatively.
VAS score is determined via using a ruler, measuring the distance on the 10-cm line between the "no pain" anchor and the patient's mark, providing a range of scores from 0-10. |
24 hours postoperatively | |
Secondary | Postoperative morphine consumption within 24 hours postoperatively | Total morphine consumption in 24 hours postoperatively will be recorded via Patient Controlled Analgesi (PCA) device. | 24 hours postoperatively |
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