Effect of dexmedetomidine combined with ultrasonic-guided sacral block on resuscitation agitation in children

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2200063285

Enrollment

Unknown

Registered

2022-09-03

Start date

2022-09-15

Completion date

Unknown

Last updated

2023-04-17

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

Conditions

Herniated, concealed penis

Interventions

The experimental group:Dexmedetomidine combined with ultrasound-guided sacral block

The control group:No

Eligibility

Sex/Gender

All

Age

No minimum to 12 Years

Inclusion criteria

Inclusion criteria: 1. ASA I-II; 2. Male and female, aged 0-10 years.

Exclusion criteria

Exclusion criteria: 1. There were obvious abnormal coagulation function; 2. Local anaesthetic allergy and history of nervous system disease; 3. Skin damage and infection lesions at the puncture site; 4. Could not cooperate with the experimenter.

Design outcomes

Primary

Measure	Time frame
Arterial blood gas;Amount of anesthetic;Sacral canal puncture time;Incidence of agitation during recovery;Degree of agitation during recovery;	—

Secondary

Measure	Time frame
Postoperative urinary retention;Postoperative nausea and vomiting;	—

Countries

China

Contacts

Public ContactRenhu Li

Liu'an Hospital Affiliated to Anhui Medical University

lirenhu2008@163.com+86 13966241616

Outcome results

None listed

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