Gynecologic Disease Clinical Trial
Official title:
Ultrasound Guided Quadratus Lumborum Block Versus Erector Spinae Plane Block For Postoperative Analgesia In Patient Undergoing Laparoscopic Hysterectomy: A Randomized Double Blinded Study
Verified date | June 2023 |
Source | Namik Kemal University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Postoperative pain following laparoscopic hysterectomy is a challenging concern as some patients suffer acute pain that could let to chronic pain over time following the surgery. Epidural analgesia which is the gold standard for postoperative pain management in abdominal surgeries including laparoscopic hysterectomy has side effects such as hypotension, hematoma, motor weakness of lower limbs, paresthesia, intrathecal placement of the epidural catheter and urinary retention that could prolong hospital stay. Since high frequency ultrasound machines' usage has increased in postoperative analgesia management, ultrasound guided fascial plane blocks has been performed by clinicians with high success rate. To avoid possible complications of epidural catheter placement and epidural analgesia, various techniques has been applying for an analgesic effect close to the effectiveness of epidural analgesia. These techniques include transversus abdominis plane block, rectus sheath block, wound infiltration of local anesthetics, erector spinae plane block and quadratus lumborum plane block . However, each of the plane blocks has limitations individually which prevent them to be the unique analgesic technique for postoperative analgesia following abdominal surgery. As far as the authors knowledge, there's no reported study which compares ultrasound guided erector spinae plane block versus ultrasound guided quadratus lumborum type III block (anterior quadratus lumborum block) as a preemptive analgesia technique in patients undergoing laparoscopic hysterectomy.
Status | Completed |
Enrollment | 81 |
Est. completion date | April 1, 2023 |
Est. primary completion date | April 1, 2023 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years to 75 Years |
Eligibility | Inclusion Criteria: - Patients who accepted to participate and signed written consent - Aged between 18 and 75 - American Society of Anesthesiologists (ASA) physical score I or II - Elective laparoscopic hysterectomy operation Exclusion Criteria: - Patients who declined to participate - BMI > 35 kg/m2 - Uncontrolled systemic disease - <18 age and >75 age - Unable to cooperate (mental retardation) - Low cardiac capacity - Hypersensitivity history to the agents to be used - Coagulopathy - Local infections - Opioid addiction history |
Country | Name | City | State |
---|---|---|---|
Turkey | Tekirdag Namik Kemal University | Tekirdag |
Lead Sponsor | Collaborator |
---|---|
Namik Kemal University |
Turkey,
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* Note: There are 15 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Total dose of opioid consumption (tramadol) | Total dose of tramadol consumption via patient controlled device | in the first 24 hour postoperatively | |
Secondary | Visual Analog Scale | On a scale of 0-10, the patient will learn to quantify postoperative pain where 0= No pain and 10= Maximum worst pain. | measured at at 30 minute, 2, 6, 12, 24th hour postoperatively | |
Secondary | The 1st time to rescue analgesic need | The time to ask for postoperative analgesia is the time from the end of operation to patient reporting Visual Analog Scale = 4. | recorded within the first 24 hour postoperatively | |
Secondary | Postoperative nausea and vomiting | Postoperative nausea and vomiting presence | recorded within the first 24 hour postoperatively |
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