Outcomes for Anesthesiologist-Led Care of Analgesic Protocol in Anorectal Surgery (NCT06015165) | Clinical Trial Compass
RecruitingNot Applicable
Outcomes for Anesthesiologist-Led Care of Analgesic Protocol in Anorectal Surgery
China216 participantsStarted 2024-09-10
Plain-language summary
This will be an open, prospective, parallel-group, randomized controlled trial. Patients scheduled for complex anorectal surgery under general anesthesia will be enrolled, and the perioperative analgesia mode led by anesthesiologists will be established. Compared with the perioperative analgesia mode led by surgeons, the efficacy and safety of analgesia, quality of life and satisfaction of patients will be evaluated. This study is aimed at the feasibility and efficiacy of anesthesiologist-led treatment mode in the management of moderate and severe pain in patients after complex anorectal surgery.
Who can participate
Age range18 Years – 85 Years
SexALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion criteria
✓. American Society of Anesthesia (ASA) grading I-III
✓. ≥18 years old
✓. Patients scheduled for complex anorectal surgery under general anesthesia, e.g., mixed hemorrhoidectomy/sclerosing agent injection/ligation, radical anal fistula resection, peri-anal abscess incision and drainage
Exclusion criteria
✕. Informed consent not obtained
✕. Allergic to general anesthetics, hydromorphone, non-steroidal anti-inflammatory drugs and other related ingredients
✕. Opioid abuse or pathological pain that requires long-term analgesic treatment
✕. History of severe asthma attack and acute phase of asthma
✕. Moderate or above ventilatory function or diffusion dysfunction
✕. Liver dysfunction reached Child B grade; Renal insufficiency reached chronic kidney disease (CKD) stage IV
What they're measuring
1
the time of recovery of work and life after surgery day