Anesthesia Clinical Trial
Official title:
Comparison of Postoperative Analgesic Effects of Ultrasonography-Guided Paravertebral Block and Subcostal Transversus Abdominis Plane Block in Patients Undergoing Laparoscopic Nephrectomy
Verified date | March 2024 |
Source | Istanbul University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Most of the patients undergoing laparoscopic partial/radical nephrectomy can experience moderate or severe postoperative pain, and inadequate control of this pain can cause negative consequences such as development of chronic pain, pulmonary and cardiac events, and side effects of long term opioid usage. Due to these adverse outcomes, ultrasonography-guided plane blocks can be beneficial for these patients to decrease opioid consumption. In this study, the investigators aim to compare ultrasonography-guided plane blocks: Paravertebral block and subcostal transversus abdominis plane block and traditional method: patient controlled analgesia with opioids. The investigators hypothesized that analgesic efficacy in both paravertebral and subcostal TAP blocks will have similar outcomes but better than traditional method.
Status | Completed |
Enrollment | 91 |
Est. completion date | February 1, 2024 |
Est. primary completion date | October 1, 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 75 Years |
Eligibility | Inclusion Criteria: - Age of 18-75 - Patients who are ASA (American Society of Anesthesiology): I-II - Patients who will have laparoscopic partial/radical nephrectomy - Patients who volunteer to participate in the study Exclusion Criteria: - Patients with any kind of coagulopathy - Patients with severe cardiac, pulmonary, renal or liver disease - Patients who have difficulty comprehending the IV PCA device - Patients with local anesthetic allergy - Patients with chronic opioid use |
Country | Name | City | State |
---|---|---|---|
Turkey | Istanbul University | Istanbul |
Lead Sponsor | Collaborator |
---|---|
Istanbul University |
Turkey,
Copik M, Bialka S, Daszkiewicz A, Misiolek H. Thoracic paravertebral block for postoperative pain management after renal surgery: A randomised controlled trial. Eur J Anaesthesiol. 2017 Sep;34(9):596-601. doi: 10.1097/EJA.0000000000000673. — View Citation
Parikh BK, Waghmare VT, Shah VR, Mehta T, Butala BP, Parikh GP, Vora KS. The analgesic efficacy of ultrasound-guided transversus abdominis plane block for retroperitoneoscopic donor nephrectomy: A randomized controlled study. Saudi J Anaesth. 2013 Jan;7(1):43-7. doi: 10.4103/1658-354X.109808. — View Citation
Qu G, Cui XL, Liu HJ, Ji ZG, Huang YG. Ultrasound-guided Transversus Abdominis Plane Block Improves Postoperative Analgesia and Early Recovery in Patients Undergoing Retroperitoneoscopic Urologic Surgeries: A Randomized Controlled Double-blinded Trial. Chin Med Sci J. 2016 Sep 20;31(3):137-141. doi: 10.1016/s1001-9294(16)30041-4. — View Citation
Schwarz F, Preusler W, Reifart N, Storger H, Hofmann M, Holscher I. [The long-term success after coronary angioplasty in old age]. Dtsch Med Wochenschr. 1993 Apr 30;118(17):609-14. doi: 10.1055/s-2008-1059369. German. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Indidence of PONV (postoperative nausea and vomiting) | Incidence of postoperative nausea and vomiting | Up to 24 hours | |
Other | Respiratuar Depression | Incidence of respiratory depression due to iv orphine in the postoperative follow-up. | Up to 24 hours | |
Other | Postoperative Ramsay Sedation Scale (RSS) | Ramsay sedation scale requires the patient to rate their sedation on a defined scale. For example, 1: anxious and agitated or restless, or both 2: cooperative, oriented and tranquil 3: responds to commands only 4: brisk response to stimulus 5: sluggish response to stimulus 6: no response to stimulus. | Up to 24 hours | |
Other | Itching | Incidence of itching due to iv morphine in the postoperative follow-up. | Up to 24 hours | |
Other | Surgeon Satisfaction | Satisfaction score, 0: very unsatisfied 3: very unsatisfied. | Up to 24 hours | |
Other | Patient Satisfaction | Satisfaction score, 0: very unsatisfied 3: very unsatisfied. | Up to 24 hours | |
Primary | Postoperative Intravenous Total Morphine Consumption | The total dosage of intravenous morphine consumption in 24 hours. | Up to 24 hours | |
Secondary | Postoperative Visual Analog Score (VAS) | A visual analog score (VAS) requires the patient to rate their pain on a defined scale. For example, 0-10 where 0 is no pain and 10 is the worst pain imaginable | Up to 24 hours | |
Secondary | Rescue analgesia administration amounts | Time of postoperative rescue analgesic requirement time. | Up to 24 hours | |
Secondary | Incidence of complications due to the regional blocks | Incidence of hematoma, pneumothorax (pleural puncture), local anesthetic toxicity, infection vs. | Up to first week | |
Secondary | Chronic postoperative pain | Patients' chronic pain will be assessed by the examiner questioning each patient about the pain status on postoperative 90th day. | Up to 90th day | |
Secondary | Lenght of Hospital Stay | Lenght of Hospital Stay | Up to first week |
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