Pain, Postoperative Clinical Trial
Official title:
Bilateral Transversus Abdominis Plane Block With or Without Magnesium for Total Abdominal Hysterectomy With or Without Salpingo-oophorectomy: a Randomized Controlled Trial
Verified date | April 2023 |
Source | Queen's University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Pain control after surgery is important for patient well-being and recovery. We are interested in determining whether we can improve the duration of action of a local anesthetic procedure (transversus abdominis plane block, or TAP block) by adding magnesium sulfate to local anesthetics given to patients after total abdominal hysterectomy with or without salpingo-oophorectomy.
Status | Terminated |
Enrollment | 86 |
Est. completion date | February 2020 |
Est. primary completion date | February 2020 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years to 75 Years |
Eligibility | Inclusion Criteria: - American Society of Anesthesiologists (ASA) rating I-III - Age 18-75 years old - Female - Undergoing elective total abdominal hysterectomy (TAH) with or without uni/bilateral salpingo-oophorectomy (BSO) under general anesthesia with a Pfannenstiel incision - Admitted to hospital postoperatively (inpatients) - Competent to provide informed consent Exclusion Criteria: - Emergency TAH ± BSO - ASA IV-V - Allergy or sensitivity to study-related medications - Taking any medications that are contraindicated for the use of any of our study drugs - Midline incision - Other regional anesthesia technique (e.g. epidural) - Morbidly Obese (BMI > 40) - Incompetent to provide informed consent - eGFR < 50 - Impaired liver function (INR > 1.5) - Pre-existing chronic pain condition requiring chronic opioid use - Significant co-existing cardiovascular disease |
Country | Name | City | State |
---|---|---|---|
Canada | Kingston General Hospital | Kingston | Ontario |
Lead Sponsor | Collaborator |
---|---|
Dr. Anthony Ho |
Canada,
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Gasanova I, Grant E, Way M, Rosero EB, Joshi GP. Ultrasound-guided transversus abdominal plane block with multimodal analgesia for pain management after total abdominal hysterectomy. Arch Gynecol Obstet. 2013 Jul;288(1):105-11. doi: 10.1007/s00404-012-2698-3. Epub 2013 Jan 6. — View Citation
Goyal P, Jaiswal R, Hooda S, Hoyal R, Lal J. Role of magnesium sulphate for brachial plexus analgesia. Internet Journal of Anesthesiology. 21(1): 1-6, 2008.
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Yousef GT, Ibrahim TH, Khder A, Ibrahim M. Enhancement of ropivacaine caudal analgesia using dexamethasone or magnesium in children undergoing inguinal hernia repair. Anesth Essays Res. 2014 Jan-Apr;8(1):13-9. doi: 10.4103/0259-1162.128895. — View Citation
* Note: There are 19 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Time to first dose of post-operative opioid | Investigators will note the time lapsed between end of surgery (when TAP block administered) and the first request for additional analgesia (given using patient controlled analgesia pumps, as is standard of care at our institution). | First occurrence during hospitalization (up to 24 hours postoperatively) | |
Primary | Cumulative opioid consumption | Investigators will record the total amount of opioid consumed between receiving the TAP block and 24 hours later. | Cumulative dose consumed at 2, 4, 6, 8, and 25 hours after receiving TAP blocks | |
Secondary | Pain score | Visual analog scales will be used to assess pain at rest and upon coughing in patients at various time points after receiving the TAP block after surgery. | 2, 4, 6, 8, and 24 hours after receiving TAP block | |
Secondary | Time to post-anesthetic care unit discharge | Investigators will note the time lapsed between a patient receiving their TAP block and when she is discharged from the PACU. | First occurrence during the initial 24 hours after surgery | |
Secondary | Nausea score | Nausea will be rated from 0 (none) to 3 (vomiting) at various time points after receiving TAP block | 2, 4, 6, 8, and 24 hours after receiving TAP block | |
Secondary | Pruritis score | Pruritis will be rated from 0 (none) to 3 (severe) at various time points after receiving TAP blocks. | 2, 4, 6, 8, and 24 hours after receiving TAP block | |
Secondary | Sensory block | Ice will be placed on each side of the abdomen and on the upper arm. The participant will be asked if she can feel the ice on her abdomen, and if it feels similar to that on her upper arm. | 30 minutes after arrival into the post-anesthetic care unit, and at 2, 4, 6, and 8 hours after receiving TAP blocks | |
Secondary | Patient satisfaction | Participants will be asked to rate their satisfaction from 1 (poor) to 4 (excellent) | At 24 hours after receiving TAP blocks | |
Secondary | Quality of Recovery score | Participants will be asked to fill out this 9-part survey, which consists of rating 9 statements related to recovery from anesthetic and surgery on a scale from 0 (not at all) to 2 (most of the time) | At 24 hours after receiving TAP blocks | |
Secondary | Side effects | Participants will be asked whether they experienced any side effects during the 24 hours between receiving TAP block and end of the study. | At 24 hours after receiving TAP blocks |
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