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Clinical study on transfusion comfort in patients with infusion heater

Clinical study on transfusion comfort in patients with infusion heater

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-17012162
Enrollment
Unknown
Registered
2017-07-27
Start date
2017-07-31
Completion date
Unknown
Last updated
2017-08-21

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

Conditions

Patients after total hysterectomy

Interventions

control group:Routine infusion nursing
experimental group:Application of infusion with heating infusion

Sponsors

Guangdong Provincial of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
40 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. in gynecological hospital patients with intravenous indwelling needle for rehydration, and the use of indwelling needles for at least two days; 2. aged 40-60 years; 3. Total hysterectomy; 4. postoperative rehydration time is greater than or equal to three days; 5. get informed consent, voluntary test, patient informed consent, see research brief and informed consent bookmark page.

Exclusion criteria

Exclusion criteria: 1. suffering from dementia or serious mental illness, can not express their feelings; 2. patients with severe systemic disease and unsuitable for experimental intervention, such as vascular, hepatic, renal, and hematopoietic diseases, have severe primary diseases; 3. patients had a history of phlebitis; 4. people with diabetes or temperature or pain disorders; 5. malignant tumor patients, severe anemia patients; 6. hypertensive patients.

Design outcomes

Primary

MeasureTime frame
VAS pain score;Kolcaba Comfort Status Scale;

Countries

China

Contacts

Public ContactHaixia He

Guangdong Provincial of Chinese Medicine

heidy08@163.com+86 13794360392

Outcome results

None listed

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