Block Clinical Trial
Official title:
Investigation of the Effect of Interfacial Pressure on Block Success During Anterior Quadratus Lumborum Block Application
Verified date | February 2021 |
Source | Bursa Yüksek Ihtisas Education and Research Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The block has been shown to be the result of abdominal analgesia as a result of application between the quadratus lumborum (QL) muscle and the leaves in the thoracolumbar fascia. In this block, local anesthetic drugs are administered between the quadratus lumborum (QL) muscle and the anterior leaf in the thoracolumbar fascia. In this way, it has been reported that it provides a good analgesia as it relieves somatic pain better in upper and lower abdominal surgeries.
Status | Completed |
Enrollment | 72 |
Est. completion date | September 15, 2020 |
Est. primary completion date | October 15, 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility | Inclusion Criteria: Patients who were in the American Society of Anesthesiologists (ASA) I-III class • Underwent laparoscopic cholecystectomy Exclusion Criteria: - Previous history of preoperative opioid use, - Allergy to local anesthetics, - The presence of any systemic infection, - Uncontrolled arterial hypertension, - Uncontrolled diabetes mellitus - Presence of infection in the block area, |
Country | Name | City | State |
---|---|---|---|
Turkey | University of Health Sciences, Bursa Yuksek Ihtisas Training and Research Hospital | Bursa |
Lead Sponsor | Collaborator |
---|---|
Bursa Yüksek Ihtisas Education and Research Hospital |
Turkey,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Interfascial Pressure (mm/hg) | Interfascial pressure will be measured the postoperative 24. hours through catheter. | 24 hours. | |
Secondary | sensory block level | After the application, the sensory block level at the 30 minutes after the block application and 30 minutes after the operation will be determined by cold test. | peroperative 3 hours | |
Secondary | Visual Analog Scale | Visual Analog Scale was used for pain.Pain intensity was measured using 0-10 cm visual analogue scale (VAS). (0=no pain, 10=intolerable pain) | Postoperative 24 hours | |
Secondary | analgesic use | analgesic use | Postoperative 24 hours |
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