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The effect of penehyclidine hydrochloride on perioperative respiratory adverse events in children with tonsil adenoidectomy

The effect of penehyclidine hydrochloride on perioperative respiratory adverse events in children with tonsil adenoidectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600116381
Enrollment
Unknown
Registered
2026-01-08
Start date
2026-01-10
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Adenoid hypertrophy, Tonsil hypertrophy

Interventions

Group P:In group P, penehyclidine hydrochloride was diluted into 0.1mg/ml, dispensed in a 10ml syringe, and the anesthesiologist administered 0.2ml/kg (i.e., penehyclidine hydrochloride 0.02mg/kg).
Group C:Group C was given 10ml normal saline, and 0.2ml/kg normal saline was given by the anaesthetist

Sponsors

Zhongda Hospital Southeast University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 12 Years

Inclusion criteria

Inclusion criteria: (1) ASA is classified as Grade I to III. (2) Age 0-12 years old; (3) It is planned to perform elective general anesthesia tonsillectomy and/or adenoidectomy.

Exclusion criteria

Exclusion criteria: (1) Congenital diseases or abnormal liver and kidney functions; (2) Chronic lung diseases (cystic fibrosis of the lung, bronchial dysplasia, pulmonary hypertension, etc.); (3) There was a severe upper respiratory tract infection before the operation; (4) Neuromuscular diseases, cerebral palsy, epilepsy; (5) Intubation has been performed or tracheotomy has been carried out; (6) Those who plan to be admitted to the ICU after the operation; (7) Glaucoma patients; (8) Family members or guardians refuse to participate.

Design outcomes

Primary

MeasureTime frame
Perioperative respiratory adverse events;

Secondary

MeasureTime frame
The timing (induction period, postoperative recovery period) and degree of respiratory adverse events;Heart rate;Acetylcholinesterase, interleukin-6 (IL-6) and interleukin-8 (IL-8);Real-time heart rate variability;Pain score (wong-baker score);Restlessness delirium score (PAED score);

Countries

CHINA

Contacts

Public ContactSun Jie

Zhongda Hospital Southeast University

dgsunjie@hotmail.com+86 25 8326 2526

Outcome results

None listed

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