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Effect of Aromatherapy on Pain, Anxiety and Satisfaction in Cannulation

T

TC Erciyes University

Status

Completed

Conditions

Hemodialysis Patients

Treatments

Other: aromatherapy
Other: placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT06382701
Kayseri

Details and patient eligibility

About

The most active members of the healthcare professionals responsible for hemodialysis units are nurses, and they have a key role in pain, anxiety and satisfaction management as they are responsible for cannulation. Therefore, complementary and integrated practices need to be implemented based on evidence to strengthen the independent role of nurses in managing pain and anxiety.

Enrollment

60 patients

Sex

All

Ages

18 to 80 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Those who are over 18 years of age,
  • Able to answer questions and communicate,
  • No hearing, vision or speech impairments,
  • Regularly undergoing hemodialysis three times a week,
  • Having arterio-venous fistula for at least 3 months,
  • Having pain during needle cannulation and scoring at least two or more points on the Visual Analogue Scale (VAS),
  • Having been on hemodialysis for at least three months,
  • Agreeing to participate in the study with their own consent,
  • Patients who are not allergic to clove oil will be included in the study.

Exclusion criteria

  • Having neuropathic pain,
  • Patients with arterio-venous fistula and loss of sensation of more than 50% in the extremity,
  • Patients with infection in the arterio-venous fistula line,
  • Patients with aneurysm or pseudoaneurysm in arterio-venous fistula,
  • Patients who have used analgesic medication/s in the last 6 hours,
  • Patients who have used sedative agent(s) in the last 6 hours,
  • Patients who used local anesthetic agents before needle intervention will not be included in the study.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

60 participants in 2 patient groups, including a placebo group

Intervention
Active Comparator group
Description:
This is the group in which 0.5-1 ml of clove oil is applied as a spray to the arterio-venous fistula area, depending on the length of the fistula, ten minutes before needle cannulation in all hemodialysis sessions for four weeks in individuals receiving standard hemodialysis treatment.
Treatment:
Other: aromatherapy
Placebo
Placebo Comparator group
Description:
This is the group in which 0.5-1 ml of aromatic clove, which does not contain active ingredients and is dissolved in pure water, is applied as a spray to the arterio-venous fistula area, depending on the length of the fistula, ten minutes before needle cannulation in all hemodialysis sessions for four weeks in individuals receiving standard hemodialysis treatment.
Treatment:
Other: placebo

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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