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Effect of Anrikefon Infusion on Postoperative Hyperalgesia in Patients Undergoing Lobectomy and Remifentanil Infusion: A Single-Center, Double-Blind, Randomized Controlled Study

Effect of Anrikefon Infusion on Postoperative Hyperalgesia in Patients Undergoing Lobectomy and Remifentanil Infusion: A Single-Center, Double-Blind, Randomized Controlled Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600116915
Enrollment
Unknown
Registered
2026-01-16
Start date
2026-02-01
Completion date
Unknown
Last updated
2026-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

hyperalgesia

Interventions

control group:intravenous 0.9% NaCl
experimental group:Intravenous injection of Anrikefon Infusion (HSK21542), dose: 1µg/kg

Sponsors

Guangdong Provincial People's Hospital(Guangdong Academy of Medical Sciences)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Patients and their families are informed and voluntarily agree to participate in the study, and have signed the informed consent form. (2) Patients scheduled to undergo elective unilateral single-port thoracoscopic lobectomy or partial lobectomy. (3) American Society of Anesthesiologists (ASA) physical status classification of I to III; aged 18 to 75 years; no restrictions on gender.

Exclusion criteria

Exclusion criteria: (1) Body Mass Index (BMI) >= 35 kg/m². (2) Known history of opioid abuse or dependence. (3) Current chronic use of opioids, antidepressants, and/or anticonvulsants. (4) Moderate to severe chronic obstructive pulmonary disease (COPD), defined as forced expiratory volume in one second (FEV1) < 50% of predicted value. (5) Chronic renal insufficiency. (6) Diabetes mellitus. (7) Peripheral neuropathy. (8) History of preoperative neoadjuvant radiotherapy or chemotherapy. (9) Inability to independently manage postoperative patient-controlled intravenous analgesia. (10) High risk for sleep apnea syndrome as assessed by the STOP-BANG questionnaire.

Design outcomes

Primary

MeasureTime frame
Incidence of surgical incision hyperalgesia;

Secondary

MeasureTime frame
Postoperative hydromorphone and rescue analgesic consumption.;Incidence of chronic postsurgical pain.;Postoperative pain scores.;Opioid-related adverse effects.;total consumption of remifentanil;Patient satisfaction.;Postoperative Quality of Recovery.;Incidence of nausea and vomiting.;Incidence of hyperalgesia contralateral to the surgical incision;Range of surgical incision hyperalgesia;

Countries

China

Contacts

Public ContactShu Haihua

Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences)

shuhaihua@hotmail.com+86 20 8370 9967

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026