Inadvertent Hypothermia or Hyperthermia in Pediatric Radiotherapy Practices Under Anesthesia

NCT ID: NCT05478850

Last Updated: 2022-10-13

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

152 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-08-01

Study Completion Date

2022-10-01

Brief Summary

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In prospective, observational cohort study, changes in body temperature will be investigated before the procedure and during recovery in Radiotherapy patients aged 0-18 years who need sedation due to childhood malignancies.

The aims of this study were to measure the incidence and magnitude of changes in body temperature in children undergoing sedation or general anesthesia for Radiotherapy, and to determine their effects on the recovery process.

Detailed Description

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Conditions

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Hypothermia; Anesthesia Hyperthermia, Anesthesia Related Radiotherapy Side Effect Childhood Cancer

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Radiotherapy under anesthesia

radiotherapy under anesthesia

Intervention Type PROCEDURE

Body temperature change will be investigated before the procedure and during recovery in Radiotherapy patients who need anesthesia due to childhood malignancies.

Interventions

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radiotherapy under anesthesia

Body temperature change will be investigated before the procedure and during recovery in Radiotherapy patients who need anesthesia due to childhood malignancies.

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* patients undergoing radiotherapy under anesthesia

Exclusion Criteria

* family refusal to participate,
* chronic nausea and vomiting complaints,
* active infection,
* apnea history,
* cardiac disease, kidney and liver failure,
* anomalies that may cause difficult airway,
* metabolic diseases,
* neurological or muscular diseases.
Minimum Eligible Age

1 Month

Maximum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Ankara City Hospital Bilkent

OTHER

Sponsor Role lead

Responsible Party

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Betül Güven

Principle Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Betül Güven Aytaç, MD

Role: PRINCIPAL_INVESTIGATOR

Ankara City Hospital Bilkent

Locations

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Ankara City Hospital

Ankara, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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E1-22-2700

Identifier Type: -

Identifier Source: org_study_id

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