Status:

NOT_YET_RECRUITING

Ice Pack and Lukewarm Gel Pad Use on Pain, Anxiety Level and Physiological Parameters

Lead Sponsor:

Tarsus University

Conditions:

Pain

Anxiety

Eligibility:

All Genders

9-18 years

Phase:

NA

Brief Summary

The study was planned as a randomized controlled experimental study to determine the effect of cold application used during surgical drain removal on pain, anxiety level and physiological parameters o...

Detailed Description

Non-pharmacologic methods can be used to reduce pain during drain removal. One of these methods is cold application. Cold application shows a local anesthetic effect in the application area by increas...

Eligibility Criteria

Inclusion

  • The child must be between the ages of 9 and 18,
  • The child does not have developmental delay (Developmental Problems: Delay in one or more of the developmental areas such as communication, social-emotional, cognitive, sensory functions, fine-rough movements, self-care, loss of function, loss of ability, loss of ability, limitation of participation in life as a result of disease)
  • Follow-up with surgical drain
  • The child does not have a chronic disease that may affect his/her life
  • Voluntariness of the parent and child to participate in the study

Exclusion

  • The child is under 9 years of age
  • Communication problems
  • Not volunteering to participate in the study
  • Presence of more than one surgical drain
  • The presence of developmental delay in the child (Developmental Problems: Delay in one or more of the developmental areas such as communication, social-emotional, cognitive, sensory functions, fine-rude movements, self-care, loss of function, loss of ability, loss of ability, restriction of participation in life as a result of disease)
  • Previous surgical procedure under general anesthesia
  • Use of any analgesic medication until at least 6 hours before the procedure

Key Trial Info

Start Date :

September 20 2024

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

May 31 2025

Estimated Enrollment :

108 Patients enrolled

Trial Details

Trial ID

NCT06600763

Start Date

September 20 2024

End Date

May 31 2025

Last Update

September 23 2024

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