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The effect of lidocaine spray and ice spray on reducing injection pain

Comparison of lidocaine spray and ice spray on the severity of pain during insertion of vascular needles in hemodialysis patients of the dialysis ward

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20201017049054N1
Enrollment
48
Registered
2020-12-27
Start date
2020-12-09
Completion date
Unknown
Last updated
2021-01-05

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

Conditions

Hemodialysis. Dependence on renal dialysis

Interventions

Intervention 1: Intervention 1: 10% lidocaine spray (10% lidocaine local anesthetic spray Sina drug) is sprayed in two puffs (20 mg) from a distance of 20 cm on the desired location. Intervention 2: I

Sponsors

Sabzevar University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: The patient is 18-65 years old. The patient needs to be hospitalized and undergo dialysis with peripheral vascular needles. The patient is aware of the time, place and person. It is possible to place vascular needles for the patient. Literacy for reading and writing. No problems in terms of verbal, mental and visual abilities. No opioid addiction or strong analgesics. Lack of sensitivity to anesthetics. No diabetes for more than 10 years.

Exclusion criteria

Exclusion criteria: The patient has a history of heart disease. The patient has skin and vascular disorders (erythema, itching, bruising, etc.) at the site of needle entry. The patient has symptoms of decreased sensation and movement in the upper limbs under catheterization. The patient has disease-related pain. The patient should take painkillers or narcotics before the venipuncture and be within the duration of the effect of these drugs.

Design outcomes

Primary

MeasureTime frame
Pain score. Timepoint: For each person, the pain is measured immediately after each spray, and at the end of the study, each person determines their pain a total of three times (once for each spray). Method of measurement: Visual Analogue Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHamid Roudsarabi

Sabzevar University of Medical Sciences

RoudsarabiH96@medsab.ac.ir+98 51 4465 1401

Outcome results

None listed

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