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Sensorial saturation measures to improve children's perioperative comfort: a randomized controlled clinical trial

Sensorial saturation measures to improve children's perioperative comfort: a randomized controlled clinical trial

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300074841
Enrollment
Unknown
Registered
2023-08-17
Start date
2023-09-01
Completion date
Unknown
Last updated
2023-08-21

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

Conditions

postoperative pain

Interventions

Sensorial Saturation Group:Oxygen mask coated with sweetener
Control group:Select a regular mask

Sponsors

The Affiliated Hospital of Southwest Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 3 Years

Inclusion criteria

Inclusion criteria: ? ASA Class I-II ? Age 1-3 ? High ligation of inguinal hernia sac or sheath process under general anesthesia in our hospital

Exclusion criteria

Exclusion criteria: ? The child was diagnosed with mental illness ? Maternal abuse of psychotropic substances during pregnancy ? Children take sedative and analgesic drugs for a long time ? General anesthesia operation not performed as planned

Design outcomes

Primary

MeasureTime frame
FLACC Pain Score;

Secondary

MeasureTime frame
Ramsay sedation score;Pediatric Anesthesia Emergence Delirium Scale;Vital signs (oxygen saturation, heart rate, non-invasive blood pressure);SAS anxiety score of accompanying family members·;Incidence of postoperative adverse events;Use of additional sedative and analgesic drugs after operation;Total hospitalization days;

Countries

China

Contacts

Public ContactMaohua Wang

The Affiliated Hospital of Southwest Medical University

1398488830@qq.com+86 189 8913 1360

Outcome results

None listed

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