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The efftct of sleep distursbence to Postoperative acute pain and inflammatory reactionafter breast cancer surgery--the Prospective cohort study

The efftct of sleep distursbence to Postoperative acute pain inflammatory reaction after breast cancer surgery--the Prospective cohort study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-RPC-17012922
Enrollment
Unknown
Registered
2017-10-09
Start date
2017-09-26
Completion date
Unknown
Last updated
2017-10-16

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

Conditions

BREAST CANCER

Interventions

control group:good sleep
experimental group:poor sleep

Sponsors

Liaocheng People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-65 years; 2. ASAI-II; 3. To be able to complete PSQI, SAS, and SDA questionnaires independently; 4. Unilateral breast cancer patients undergoing surgery.

Exclusion criteria

Exclusion criteria: 1. Anxiety and depression patients; 2. patients with sleep apnea syndrome, chronic pain, endocrine disease, mental illness, and acerebrovascular disease.

Design outcomes

Primary

MeasureTime frame
Postoperative pain VAS score;—

Secondary

MeasureTime frame
inflammatory factor;—

Countries

China

Contacts

Public ContactJinping Wang

Liaocheng People's Hospital

wjp102@163.com+86 0636 8276414

Outcome results

None listed

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