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Effect of CYP3A4*1G and ABCB1-C3435T genetic polymorphism on the pharmacokinetics of sulfentanil during the Laryngocarcinoma radical surgery and the postoperative patient-controlled analgesia with sulfentanil in laryngocarcinoma patients

Effect of CYP3A4*1G and ABCB1-C3435T genetic polymorphism on the pharmacokinetics of sulfentanil during the Laryngocarcinoma radical surgery and the postoperative patient-controlled analgesia with sulfentanil in laryngocarcinoma patients

Status
Active, not recruiting
Phases
Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900024854
Enrollment
Unknown
Registered
2019-07-31
Start date
2019-08-30
Completion date
Unknown
Last updated
2019-08-27

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

Conditions

Genetic Polymorphism

Interventions

Sponsors

Department of Anesthesiology of Xijing Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
40 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1) From March 2019, patients who are scheduled to undergo general anesthesia and radical laryngeal cancer resection in the Department of Otolaryngology Head and Neck Surgery, Xijing Hospital, Air Force Military Medical University, aged 40-70 years; ASA II-III grade; 2) The informed consent has been signed; 3) Patients received sufentanil intravenous analgesia after operation.

Exclusion criteria

Exclusion criteria: 1) Liver and kidney dysfunction (such as ALT > 40U/L, STB > micromol/L, etc.); 2) Combination of nephrotoxic drugs (amphotericin B, aminoglycoside antibiotics, etc.); 3) Take CYP3A enzyme inducers or inhibitors (such as rifampicin, macrolides, etc.) within 2 weeks before administration; 4) Complications such as acute infection; 5) Take other drugs that can cause abnormal liver function, such as chloramphenicol, chlorpromazine, etc.; 6) Patients with other diseases that can cause abnormal liver function, such as viral hepatitis, alcoholic liver disease, autoimmune hepatitis, respiratory tract diseases causing hypoxia, bacteremia, etc.; 7) Smoking, alcoholism, diabetes, severe cardiovascular disease, chronic kidney disease, chronic pain history, long-term use of analgesics, etc.; 8) Failure to comply with or unwilling to cooperate, and unclear understanding of the language used in the study; 9) Have participated in this study or other clinical studies at the same time.

Design outcomes

Primary

MeasureTime frame
Sufentanil consumption;

Countries

China

Contacts

Public ContactZeng Yi

Xijing Hospital, the Fourth Military Medical University

zengyi1014@163.com+86 13991267646

Outcome results

None listed

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