Development and Application of a Postoperative Pain Management Protocol for OSAHS Patients Based on the Timing Theory

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2600128699

Enrollment

Unknown

Registered

2026-07-24

Start date

2026-08-01

Completion date

Unknown

Last updated

2026-08-03

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

Conditions

Obstructive sleep apnea-hypopnea syndrome

Interventions

Intervention group:On the basis of the conventional postoperative pain management plan, a postoperative pain management plan based on the timing theory was implemented.

Control group:Conventional postoperative pain management plan

Eligibility

Sex/Gender

All

Age

18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1.Meets the diagnostic criteria for obstructive sleep apnoea-hypopnoea syndrome (OSAHS); 2.Age range from 18 to 60 years old; 3.Planned uvulopalatopharyngoplasty under general anaesthesia; 4.Sign the informed consent form to voluntarily participate in this study.

Exclusion criteria

Exclusion criteria: 1.Individuals without a history of chronic underlying conditions such as diabetes, hypertension, or coronary heart disease, and those with severe systemic illnesses. 2.Individuals with addiction and tolerance to opioid medications; 3.Individuals with hypotension, hypothyroidism, asthma, benign prostatic hyperplasia, and epilepsy.

Design outcomes

Primary

Measure	Time frame
Postoperative pain intensity;	—

Secondary

Measure	Time frame
Postoperative swallowing function;Postoperative sleep quality;General information of the participants;	—

Countries

China

Contacts

Public ContactZhang Wenyun

Affiliated Hospital of Hangzhou Normal University

174529603@qq.com+86 571 88303412

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026