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Clinical Trials in Turkey / NCT06988748
Starting soon Not applicable

Diet Education and Postoperative Outcomes in Pediatric Adenotonsillectomy

NCT06988748 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-06-20
Last updated
2025-06-04

Condition(s) studied

Adenotonsillar Hypertrophy

Investigational drug(s) / intervention(s)

Assigned Interventions (diet training)

Assigned Interventions (diet training): Pain and bleeding will be evaluated at 4 hours, 8 hours, 24 hours and 7 days after adenotonsillectomy by using "Wong-Baker Faces Pain Rating Scale" and "Follow-up and Evaluation Form for Children After Adenotonsillectomy in Children".

Study summary

This randomized controlled trial aims to evaluate the effect of tonsillectomy diet education on postoperative bleeding and pain in children undergoing adenotonsillectomy. Seventy-six pediatric patients will be randomly assigned to either an intervention group, which will receive specific diet education prior to surgery, or a control group receiving standard care. Bleeding and pain will be assessed at 4, 8, and 24 hours, and on the 7th day after surgery using a specialized follow-up form and the Wong-Baker Faces Pain Rating Scale. The study hypothesizes that diet education will reduce postoperative bleeding and pain, improving recovery and quality of life in children.

Eligibility

Sex
ALL
Min age
—
Max age
18 Years
Healthy volunteers
Accepted
Inclusion Criteria: * The child being sick, * The child will have an adenotonsillectomy, * The child has no milk allergy (to exclude children at risk of developing milk allergy during the data collection process), * The child's caregiver stays with the child during the research process (to avoid communication barriers and disruptions in treatment and care instructions during the training and data collection process), * The child and caregiver can speak and understand Turkish (to avoid communication barriers during the training and data collection process), * The child's caregiver agrees to the research, * Children without swallowing difficulties and aspiration risk (e.g. nasogastric catheter, tracheostomy) * Children without diseases that cause maladaptive behavior (e.g. autism, cerebral palsy) Exclusion Criteria: * The child has a milk allergy, * Children with diseases that cause swallowing difficulties, risk of aspiration and maladaptive behavior (e.g. autism, cerebral palsy) * Failure of the child and caregiver to attend the follow-up examination on the 7th day after surgery

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Hilal AKDENİZ Istanbul Ataşehir

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06988748 on ClinicalTrials.gov ↗ ← All trials in Turkey