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Determination of the Effect of Cold Needle on Invasive Pain Cannulation

Determination of the Effect of Cold Needle Application on Invasive Pain Associated With Fistula Cannulation

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06418009
Enrollment
35
Registered
2024-05-16
Start date
2024-04-20
Completion date
2024-05-20
Last updated
2024-05-16

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

Conditions

Hemodialysis Complication, Pain

Brief summary

In studies evaluating the methods used to reduce invasive pain associated with cannulation, it is seen that pharmacological and non-pharmacological methods are used. Pharmacological treatment is considered risky as it may cause drug addiction in the patient and may cause side effects and complications. On the other hand, the use of non-pharmacological methods is preferred because they are cheaper and cause fewer side effects and complications.

Detailed description

Cold application, one of the non-pharmacological methods used, is effective in relieving pain by slowing down or blocking the conduction of peripheral nerves. Apart from this effect, it stimulates touch receptors by activating the Door-Control mechanism; It increases the release of endogenous opioids and stops pain by ensuring the nerve impulses caused by cold are transmitted to Delta fibers. Although studies conducted on hemodialysis patients have shown that cold application is effective in reducing pain; Due to the small number of sample groups and deficiencies in the methodology, it was suggested that further studies be conducted. In these studies, cold application; It was applied to the area one cm above the fistula or between the thumb and index finger of the opposite arm, using an ice pack and an ice-filled glove for 2-10 minutes.

Interventions

PROCEDURECold needle application

Before use, the needle will be removed from the refrigerator and kept on the nurse's table. When the temperature of the needle reaches 0-2 °C, the patient will be cannulated.

Sponsors

Istanbul Demiroglu Bilim University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Masking description

Pain assessment will be made by a nurse independent of the study

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* patients aged 18 years and older * had been treated with HD for at least 3 months, thrice a week, and for 4 hours per session * did not have a psychiatric disorder that would prevent communication * volunteered to participate in the study

Exclusion criteria

* Patients who were known to present difficulties when entering the fistula (requiring multiple cannulations) * had a history of hematoma or stenosis in the AVF * had an infection at the fistula site * took painkillers within 3 hours of treatment * did not want to participate in the study

Design outcomes

Primary

MeasureTime frameDescription
Invasive painUp to two weeksIt will be assessed three times at the end of the dialysis session with Visual Analogue. Pain intensity measured on a Visual Analog Scale with scores ranging from 0 - 10. Pain increases as the score increases. The high point describes bad outcome

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026