Evaluating the Effect of the Valsalva Maneuver on Invasive Pain During Arteriovenous Fistula Cannulation in Hemodialysis Patients

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorCansu POLAT DÜNYA

About this trial

The goal of this clinical trial is to evaluate whether the Valsalva maneuver reduces invasive pain during arteriovenous fistula (AVF) cannulation in adult hemodialysis patients. The main questions it aims to answer are:

Does the Valsalva maneuver effectively reduce pain intensity during AVF cannulation as measured by the Visual Analogue Scale (VAS)?

Is the Valsalva maneuver feasible, acceptable, and satisfactory for patients, and can it be sustainably implemented over multiple sessions?

Researchers will compare patients performing the Valsalva maneuver (intervention group) with those receiving standard care without any intervention (control group) to see if pain scores are significantly lower and whether patients are willing to continue using this technique voluntarily.

Participants will:

Receive training and supervised practice on the Valsalva maneuver before inclusion in the study

Perform the Valsalva maneuver during AVF cannulation in each hemodialysis session for 12 sessions

Complete VAS pain assessments after each session

Complete a patient satisfaction and feasibility form at the end of the study

Eligibility criteria

Qualifiers

Age 18 years or older

Receiving hemodialysis treatment via arteriovenous fistula for at least 3 months

No analgesic medication use within the past 24 hours

Systolic blood pressure between 90-160 mmHg and diastolic between 60-100 mmHg

Disqualifiers

Unable to correctly perform the Valsalva maneuver

Failed first cannulation attempt

History of acute myocardial infarction or malignant arrhythmia

Aneurysm, infection, edema, or scar tissue at AVF site

Trial design

Treatments tested in this trial

  • Valsalva Maneuver

Treatment groups

60 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators

Cansu POLAT DÜNYA

Lead sponsor

Istanbul University

Sponsor institution

Istanbul University Scientific Research Projects Coordination Unit- Pending

Collaborator