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Clinical study of s-ketamine in pediatric outpatient sedation

Clinical study of s-ketamine in pediatric outpatient sedation

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200060976
Enrollment
Unknown
Registered
2022-06-14
Start date
2022-06-01
Completion date
Unknown
Last updated
2023-03-26

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

Conditions

pediatric outpatient sedation

Interventions

3:Different doses of s-ketamine nasal drops

Sponsors

Hunan Children's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 8 Years

Inclusion criteria

Inclusion criteria: Patients with clinical sedation who were classified as ASA grade ?-? and planned to undergo cardiac color doppler examination

Exclusion criteria

Exclusion criteria: The child was associated with chromosomal diseases, severe pulmonary hypertension, cyanosis and other manifestations before sedation, ASA grade ? or above, increased intracranial pressure, age (corrected gestational age) =3 months and weight =5kg

Design outcomes

Primary

MeasureTime frame
Ramsay sedation score;Steward awakening Score;

Secondary

MeasureTime frame
HR;SPO2;

Countries

P.R.China

Contacts

Public ContactDongjie Pei
jerrypei_16@hotmail.com15673227688

Outcome results

None listed

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