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Effect of fentanyl and sufentanil on PACU retention time after laparoscopic hernia repair in children

Effect of fentanyl and sufentanil on PACU retention time after laparoscopic hernia repair in children

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300072177
Enrollment
Unknown
Registered
2023-06-06
Start date
2022-02-28
Completion date
Unknown
Last updated
2023-06-12

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

Conditions

hernia

Interventions

S1:General anesthesia was induced with sufentanil 0.2ug/kg in children aged 2 to 6 years
F1:General anesthesia was induced with fentanyl 2ug/kg in children aged 2 to 6 years
S2:General anesthesia was induced with sufentanil 0.2ug/kg in children aged 6 to 12 years
F2:General anesthesia was induced with fentanyl 2ug/kg in children aged 6 to 12 years

Sponsors

Hubei Maternal and Child Health Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to 12 Years

Inclusion criteria

Inclusion criteria: 1) Prior to performing any examination, sampling, or analysis related to the study, written informed consent of the subject's legal guardian has been obtained (2) for patients aged 2-12 years (3) who intend to undergo laparoscopic hernia repair under general anesthesia (4)ASA grade ?-?

Exclusion criteria

Exclusion criteria: (1) Patients with chronic pain disease and long-term use of sedative and analgesic drugs (2) drug abuse, drug and alcohol addiction (3) patients who took sedative and analgesic drugs 24h before surgery (4) patients with previous history of sleep disorders and obstructive sleep apnea syndrome (5) patients with high blood risk, For example, patients with congenital bleeding diseases (such as hemophilia), thrombocytopenia (PLT 1.5×ULN or creatinine clearance mL/min(9) Speech disorders, visual and hearing disorders, muscle strength abnormalities, inability to communicate with others, inability to take care of themselves, and difficulty in conducting Steward score, such as congenital muscle atrophy patients. (10) Participated in other clinical studies 3 months before randomization

Design outcomes

Primary

MeasureTime frame
Steward Score;

Secondary

MeasureTime frame
extubation time;

Countries

China

Contacts

Public ContactwenChen

Hubei Maternal and Child Health Hospital

2116628669@qq.com+86 186 7233 6018

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 7, 2026