Perioperative pain management based on enhanced recovery after surgery in children with obstructive sleep apnea

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100044771

Enrollment

Unknown

Registered

2021-03-27

Start date

2021-03-26

Completion date

Unknown

Last updated

2022-08-23

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

Conditions

Obstructive sleep apnea

Interventions

Control group:Nil

ERAS group:Enhanced Recovery After Surgery (ERAS)

Eligibility

Sex/Gender

All

Age

2 Years to 9 Years

Inclusion criteria

Inclusion criteria: Children with tonsil or adenoid hypertrophy associated with obstructive sleep apnea syndrome.

Exclusion criteria

Exclusion criteria: Patients or their parents who were unwilling to accept the enhanced recovery after surgery (ERAS).

Design outcomes

Primary

Measure	Time frame
The pain scores and diet quality scores;	—

Countries

China

Contacts

Public ContactZhang Yu

Department of Otolaryngology, Head and Neck Surgery. Yantai Yuhuangding Hospital, Qingdao University, Yantai, China

yangyujuanyyj@163.com+86 13792527677

Outcome results

None listed

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