Determination of the Effective Dose of a Single Intravenous Dose of Tegileridine Fumarate for Postoperative Analgesia After Orthopedic Surgery: A Up-and-Down Sequential Allocation Study

Recruiting now · Phase 4

Conditions studied: Postoperative Pain

In brief

The goal of this clinical trial is to determine the 90% effective dose (ED90) of a single intravenous injection of tegileridine fumarate for postoperative analgesia in adult patients aged 18-75 years with American Society of Anesthesiologists (ASA) physical status I-III undergoing orthopedic surgery, including spinal fusion surgery, femoral fracture fixation, and total knee arthroplasty. The main questions this study aims to answer are: What is the ED90 of a single intravenous dose of tegileridine fumarate for achieving adequate postoperative analgesia, defined as a Numeric Rating Scale (NRS) pain score ≤ 3 within 30 minutes after awakening from anesthesia without the need for rescue analgesia? Participants will: Receive a single intravenous injection of tegileridine fumarate during skin closure at the end of surgery. Start with an initial dose of 0.5 mg, with subsequent doses adjusted upward or downward in 0.1 mg increments for the next participant based on the analgesic response of the preceding participant, following a biased-coin up-and-down sequential dose allocation design. Be closely monitored during the postoperative recovery period for pain intensity, vital signs (including heart rate, blood pressure, respiratory rate, and oxygen saturation), and adverse reactions such as nausea, vomiting, respiratory depression, agitation, and other opioid-related side effects. This study aims to identify an optimal single-dose regimen of tegileridine fumarate that provides effective postoperative analgesia with an acceptable safety profile, thereby improving postoperative pain control and promoting enhanced recovery in patients undergoing orthopedic surgery.

Key facts

Study ID: NCT07353996
Run by: Second Affiliated Hospital, Zhejiang University, School of Medicine
People needed: 180
Starts: 2025-10-25
Expected to finish: 2026-05-01
Last updated by the study team: 2026-01-21

Who can join

Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Adults aged 18 to 75 years.
Scheduled for elective orthopedic surgery, including spinal fusion, femoral fracture fixation, or total knee arthroplasty.
American Society of Anesthesiologists (ASA) physical status I-III.
Ability to understand the study procedures and provide written informed consent.

You may not qualify if…

Patients with moderate to severe obesity (BMI > 30 kg/m²).
Known hypersensitivity or allergy to tegileridine fumarate or other analgesics.
History of chronic pain or long-term use of opioids.
Severe hepatic or renal impairment.
Patients requiring postoperative ICU care.
Severe respiratory depression (e.g., oxygen saturation < 90%).
Known or suspected gastrointestinal obstruction, including paralytic ileus.

Where it is running

The Second Affiliated Hospital of Zhejiang University anesthesiology department — Hanzhong, Zhejiang, China (enrolling)

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.