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Comparative study of Valsalva maneuver and EMLA ointment on pain intensity due to fistula cannulation

Comparison of Valsalva maneuver and EMLA ointment in terms of their effectiveness on the pain of vascular needles insertion in hemodialysis patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20120109008665N12
Enrollment
75
Registered
2020-06-13
Start date
2020-07-05
Completion date
Unknown
Last updated
2020-06-15

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

Conditions

Acute pain. Other acute postprocedural pain

Interventions

Intervention 1: Intervention group: The first group made use of EMLA cream, made by Astrazeneca,Eczacibasi Ltd, Turkey. Cream surface is covered by a piece of paper and a 2 cc syringe was used to appl

Sponsors

Semnan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Age over 18 years History of at least 3 months of hemodialysis No addiction or dependence on painkillers No pain before cannulation Do not use the sedative at the last 24 hours No wounds in the fistula area No history of skin allergies, or dermatitis Not treated with sulfonamides, nitrates and phenobarbital Not having a pacemaker No history of Alzheimer's disease, dementia, peripheral vascular disease, diabetic neuropathy, liver disease Lack of respiratory problems, brain problems, glaucoma, increased intracranial pressure and recent eye surgery

Exclusion criteria

Exclusion criteria: Patients who are unable to perform the Valsalva maneuver by holding the mercury column above 20 mm Hg for 20 seconds Unsuccessful cannulation in the first step and repeated insertion of the needle into the skin Patients with known heart attack or those with hemodynamic problems or dangerous arrhythmias

Design outcomes

Primary

MeasureTime frame
The severity of the pain. Timepoint: The first stage without intervention - the second stage after the intervention. Method of measurement: Visual Analogue Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHassan Babamohamadi

Semnan University of Medical Sciences

babamohammady2007@gmail.com+98 23 3365 4192

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 11, 2026