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Evaluation of the Effects of Oliceridine in Anesthesia for Adenotonsillectomy in Children

Evaluation of the Effects of Oliceridine in Anesthesia for Adenotonsillectomy in Children

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400094590
Enrollment
Unknown
Registered
2024-12-25
Start date
2025-01-04
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

Adenoid hypertrophy and tonsillitis

Interventions

Oliceridine group:Anesthesia induction is induced with only oxelidine
Sufentanil group:Anesthesia induction is induced with sufentanil only

Sponsors

Guilin People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 12 Years

Inclusion criteria

Inclusion criteria: 1.Children aged 3-12 years who require adenoid or tonsil surgery. 2.Body weight between 14-40 kg. 3.ASA classification of I to II according to the American Society of Anesthesiologists. 4.Patients and parents agree to participate in the study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Presence of severe cardiopulmonary diseases or other systemic conditions affecting anesthesia. 2.Known allergy to Oliceridine. 3.Recent treatment with other medications that may affect pain assessment. 4.Family member of the child requests to withdraw from the study protocol.

Design outcomes

Primary

MeasureTime frame
Anesthesia recovery time;Time to postoperative extubation;

Secondary

MeasureTime frame
Postoperative pain VAS score;Postoperative Agitation PAED Score;

Countries

China

Contacts

Public ContactYuping Qin

Guilin People's Hospital

1938834189@qq.com+86 182 7632 1636

Outcome results

None listed

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