Investigation of the risk factors of perioperative sleep disorders in orthopaedic surgery

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR1900023756

Enrollment

Unknown

Registered

2019-06-10

Start date

2019-07-01

Completion date

Unknown

Last updated

2019-06-17

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

Conditions

sleep disorders

Interventions

somnipathy group+ non-somnipathy group:no intervention

Eligibility

Sex/Gender

All

Age

18 Years to 100 Years

Inclusion criteria

Inclusion criteria: The patient who suffer from orthopaedic surgery using general anesthesia, intraspinal anesthesia, or nerve block anesthesia is included in the experiment.

Exclusion criteria

Exclusion criteria: The patient who complicated with mental diseases, cerebrovascular diseases, hyperthyroidism, hypothyroidism, Parkinson's disease or taking anti-anxiety drugs and sedative drugs is excluded from the experiment. The patients who is unable to listen and see.

Design outcomes

Primary

Measure	Time frame
sleep;	—

Secondary

Measure	Time frame
Mini-Mental State Examination;surgery time;the type of anesthesia;medicine;complication;BMI;other disease which have no relationship with surgery;amount of blood;outcome;	—

Countries

China

Contacts

Public ContactWenqin Song

Renmin Hospital of Wuhan University

wenqi-1987@163.com+86 18627767054

Outcome results

None listed

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