Actively Recruiting

Phase Not Applicable
Age: 18Years - 85Years
All Genders
NCT06015165

Outcomes for Anesthesiologist-Led Care of Analgesic Protocol in Anorectal Surgery

Led by China-Japan Friendship Hospital · Updated on 2024-11-13

216

Participants Needed

2

Research Sites

56 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Outcomes for Anesthesiologist-Led Care of Analgesic Protocol in Anorectal Surgery

Who Can Participate

Age: 18Years - 85Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • American Society of Anesthesia (ASA) grading I-III
  • 18 years or older
  • Scheduled for complex anorectal surgery under general anesthesia, such as mixed hemorrhoidectomy, sclerosing agent injection, ligation, radical anal fistula resection, or peri-anal abscess incision and drainage
Not Eligible

You will not qualify if you...

  • Informed consent not obtained
  • Allergy to general anesthetics, hydromorphone, non-steroidal anti-inflammatory drugs, or related ingredients
  • History of opioid abuse or pathological pain requiring long-term analgesic treatment
  • History of severe asthma attack or in the acute phase of asthma
  • Moderate or worse ventilatory function or diffusion dysfunction
  • Liver dysfunction at Child B grade or renal insufficiency at chronic kidney disease stage IV
  • Gastric retention or paralytic ileus
  • Pregnant or lactating patients

AI-Screening

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Trial Site Locations

Total: 2 locations

1

China-Japan Friendship Hospital

Beijing, Beijing Municipality, China, 100029

Actively Recruiting

2

Department of Anesthesiology

Beijing, Beijing Municipality, China, 100029

Actively Recruiting

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Research Team

L

Li Fang WANG, Doctor

CONTACT

M

Meng Tao ZHENG, Doctor

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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