Effect of Sesame Oil in Preventing Phlebitis

Ç

Çukurova University

Status

Completed

Conditions

Phlebitis After Infusion

Treatments

Other: Complementary treatment practice

Study type

Interventional

Funder types

Other

Identifiers

NCT05326568
CukurovaUnıversıty-Mgulsen-01

Details and patient eligibility

About

Background: To determine the effect of sesame oil in preventing phlebitis that may occur during intravenous therapy in patients undergoing cardiac surgery. Material and Method: A randomized controlled interventional study will be conducted with patients treated in the coronary intensive care unit of a university hospital. The population of the study will be the patients hospitalized in the intensive care unit after cardiac surgery and administered parenteral amiodarone infusion. The power analysis was carried out by taking the study by. The sample size was determined as 44 patients. Personal Information Form and Visual Infusion Phlebitis Scale will be used to collect data. Sesame oil will be applied to the patients in the intervention group as 10 drops, 10 cm around the cannula, for 10 minutes. This administration will be repeated every eight hours during the 24-hour amiodarone infusion. No application will be made by the researcher to the patients in the control group. At the end of each 24 hours, patients in both groups will be evaluated by the investigator on the Visual Infusion Phlebitis Scale. Descriptive statistics, chi square, independent t test and Fisher's exact test will be used to evaluate the data.

Full description

No application was made to the patients assigned to the control group. Sesame oil was applied by the researcher to the patients assigned to the intervention group. Sesame oil was applied to the 10 cm circumference of the cannula by applying 10 drops and 10 minutes. This application was repeated every eight hours during the 24-hour amiodarone infusion. The area where the intravenous line is located is covered with a standard transparent dressing (Tegaderm) so that it can be observed. Patients in the intervention and control groups were evaluated for phlebitis at the end of every 24 hours (1st day, 2nd day, 3rd day) according to the VIP scale. The highest of the phlebitis stages obtained as a result of the evaluation was accepted as the final evaluation.

Enrollment

44 patients

Sex

All

Ages

18 to 75 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients who had undergone cardiac surgery,
  • were over 18 years old,
  • were conscious, could communicate,
  • were not allergic to sesame,
  • were administered prophylactic rhythm regulator
  • amiodarone as a treatment were included in the study.

Exclusion criteria

  • who was with cancer,
  • who was with diabetes mellitus,
  • who was with hypertension
  • who was with peripheral vascular disease
  • Patients who had myocardial infarction during the procedure,
  • Received immunosuppressive therapy,
  • underwent resuscitation and could not use an intravenous catheter for any reason

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

44 participants in 2 patient groups

Experimental
Experimental group
Description:
Sesame oil was applied by the researcher to the patients assigned to the intervention group. Sesame oil was applied to the 10 cm circumference of the cannula, in the form of 10 drops and 10 minutes.
Treatment:
Other: Complementary treatment practice
Control
No Intervention group
Description:
No treatment was applied to the patients assigned to the control group and only standard care was applied.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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