Skip to content

Construction and verification of perioperative "analgesia cloud ward" management mode in HIV-infected patients

Construction and verification of perioperative "analgesia cloud ward" management mode in HIV-infected patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500097998
Enrollment
Unknown
Registered
2025-02-28
Start date
2023-03-20
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

HIV Perioperative Pain

Interventions

treatment group:Patients were managed using the "analgesic cloud ward" management model. These include (1) the Internet of Things based on ZigBee technology to establish an intelligent analgesia elect
(2) patients use personal intelligent terminals to self-assess the degree of pain
(3) full-time pain management doctors in the Department of Anesthesiology are responsible for the diagnosis and treatment of postoperative pain in patients
and (4) pain management nurses in the Department of Anesthesiology are responsible for postoperative follow-up and education of patients.
control group:The control group used the conventional pain management model. Postoperative PCA was routinely configured in the traditional mode, with no intelligent functions such as real-time feedbac

Sponsors

Beijing Ditan Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Confirmed HIV infection by immunological and virological tests; 2. Scheduled for elective surgery; 3. Aged 18 to 75 years old; 4. Clear consciousness and able to communicate autonomously;

Exclusion criteria

Exclusion criteria: 1. Patients with uncontrolled hypertension, uncontrolled diabetes, cardiac dysfunction (NYHA heart function II-III) and other serious systemic diseases and mental illness history; 2. Pregnant or lactating; 3. After explanation, patients do not understand the purpose and significance of the project, do not actively cooperate; 4. Unable to sign informed consent.

Design outcomes

Primary

MeasureTime frame
Incidence of moderate to severe pain ;

Secondary

MeasureTime frame
Pain conditions;anxiety level;depression level;postoperative nausea and vomiting, PONV;sedation level;Postoperative respiratory depression;

Countries

China

Contacts

Public ContactCheng Hao

Beijing Ditan Hospital, Capital Medical University

chenghaocn@yahoo.com+86 138 0131 2117

Outcome results

None listed

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