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An experimental study comparing the time of application of warm therapy to reduce pain, anxiety, and side-effects during randomized extraction of patients with chronic renal failure

Comparison of Pain, Anxiety, and Side Effect According to the Application Time of Warming Therapy during Arteriovenous Fistula Puncture: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0004264
Enrollment
80
Registered
2019-08-30
Start date
2019-05-27
Completion date
Unknown
Last updated
2019-12-16

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

Conditions

None listed

Interventions

Medical Device, Others : After describing the purpose and method of the study to the subject, the subjects who agreed to the study will be randomly assigned to groups A, B, and C with a number-sealed

Sponsors

Sunchon National University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Selection Criteria (1) Those who understand the purpose of this study and agree to participate in the study (2) Those who have received hemodialysis regularly for more than 3 months in an arteriovenous fistula (3) An adult patient aged 20 years or older who has no mental deficiencies and can understand and answer the contents of the experiment, (4) A person who does not have an inflammatory or dermatological history of the venous puncture site (5) Patients who do not receive other pain relievers for arteriovenous fistula

Exclusion criteria

Exclusion criteria: Exclusion criteria (1) complications associated with arteriovenous fistulas, such as surgery or surgery (2) If you have hypersensitivity reactions and circulatory disorders (3) Experience with application of on-therapy to puncture site of arteriovenous fistula (4) When taking pain medication by disease (within 6 hours of pain medication) When selecting a subject, I will seek advice from a nephrology internist and a nurse.

Design outcomes

Primary

MeasureTime frame
Anxiety;pain

Secondary

MeasureTime frame
Side effects

Countries

Korea, Republic of

Contacts

Public ContactYANGOK BACK

Sunchon National University

21kiknai@naver.com+82-61-689-9595

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 25, 2026