Postoperative Recovery Quality With Anricofen plus Ciprofol vs Sufentanil plus Ciprofol in ERCP under Non-intubated Anesthesia

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is a single-center, prospective, randomized study enrolling adults 18 to 80 who are scheduled for elective ERCP. Participants are assigned 1:1 to receive either anricofen 1 μg/kg before ciprofol induction or sufentanil 0.1 μg/kg before ciprofol induction, with ciprofol used for induction and maintenance. The primary outcome is the QoR-15 score at 24 hours post-procedure; secondary outcomes include postoperative pain and other recovery parameters. The study aims to compare recovery quality and safety between the two anesthesia regimens in non-intubated ERCP patients. It is led by The First Affiliated Hospital of Xinxiang Medical College, with sites at The First Affiliated Hospital of Henan Medical University in Xinxiang, Henan.

Why it matters

Who can join: the full rules

\*\*Inclusion Criteria:\*\*

1. Aged 18 to 80 years;
2. American Society of Anesthesiologists (ASA) physical status I to III;
3. Patients scheduled to undergo elective endoscopic retrograde cholangiopancreatography (ERCP).

\*\*Exclusion Criteria:\*\*

1. Pregnancy or lactation;
2. Obstructive sleep apnea (OSA);
3. Long-term use of analgesics or psychotropic drugs, or a history of drug abuse;
4. Coagulation dysfunction, bleeding tendency, or current anticoagulant therapy;
5. Allergy to any of the study drugs;
6. Severe cardiac, hepatic, renal, or other major organ diseases;
7. Mental or cognitive impairment that prevents cooperation with the assessment;
8. Inability to comply with the study protocol or complete follow-up;
9. Requirement for tracheal intubation, postoperative transfer to the intensive care unit (ICU), or postoperative pancreatitis.

Where it's running

• The First Affiliated Hospital of Henan Medical University
  Xinxiang, Henan, China Recruiting

Study contacts

• Study coordinator: Longhua Guo
• Email: 1535732839@qq.com
• Phone: 18303733012

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.