Ignite Creation Date:
2024-10-26 @ 3:37 PM
Last Modification Date:
2024-10-26 @ 3:37 PM
Study NCT ID:
NCT06550869
Status:
RECRUITING
Last Update Posted:
None
First Post:
2024-08-07
Brief Title:
Application of Anterior Quadratus Lumborum Block at the Lateral Supra-arcuate Ligament Under Laparoscopic Direct Vision in Laparoscopic Renal Surgery
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Application of Anterior Quadratus Lumborum Block at the Lateral Supra-arcuate Ligament Under Laparoscopic Direct Vision in Laparoscopic Renal SurgeryA Randomized Controlled Trial
Status:
RECRUITING
Status Verified Date:
2024-07
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Evaluation of the effectiveness of Anterior Quadratus Lumborum Block at the lateral supra-arcuate ligament under laparoscopic direct vision compared to local infiltration anesthesia for postoperative analgesia after laparoscopic renal surgery in patientsA randomized controlled trial involving 66 patients undergoing laparoscopic renal surgery will assign them randomly to an experimental group or a control groupThe patients in experimental group will receive Anterior Quadratus Lumborum Block at the lateral supra-arcuate ligament under laparoscopic direct visionThe patients in control group will receive local infiltration anesthesiaThe primary outcome measure is the cumulative consumption of intravenous morphine equivalents at postoperative 24 hoursThe secondary outcomes include the cumulative consumption of intravenous morphine equivalents at postoperative 2 4 6 12 and 48 hours Numeric Rating ScaleNRS score at rest and during activity coughing at postoperative 2 6 24 and 48 hours Global Comfort QuestionnaireGCQ Comfort Status Scale Score Quality of Recovery-15QoR-15 Postoperative Recovery Scale Score time of the first press on the Patient-Controlled Analgesia pump nausea vomiting skin itching drowsiness or other adverse reactions regional anesthesia-related complications such as local anesthetic toxicity and length of postoperative hospital stay after surgery
Detailed Description:
The patients were 11 randomly assigned into groups by a clinical researcher not involved in the clinical procedures or data collection The random numbers were generated by R studio 410 R studio Boston MA USA software in a 11 ratio with a block size of 8 for each group The generated random numbers were sealed in opaque envelopes with sequential numbers On the day of surgery the envelope was opened by the protocol executor according to the recruitment order before the induction of general anesthesiaData collection is in the charge of special personnel and Case Report Form shall be filled in timely after data collection At the same time the electronic database was edited by Excel and the electronic database was entered timely after filling in the paper Case Report form
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None