Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 2:22 AM
Ignite Modification Date:
2025-12-25 @ 2:22 AM
NCT ID:
NCT07011134
Eligibility Criteria:
Inclusion Criteria:
* Age from 4 to 12 years.
* Both sexes.
* American society of Anesthesiologist (ASA) physical status I-II.
* Scheduled for pediatric ambulatory elective surgical procedures lasting ≤ three hours duration.
Exclusion Criteria:
* Parents refusal to participate.
* Conditions and diseases interfering with ambulatory day case surgery e.g., significant respiratory diseases, morbid obesity, obstructive sleep apnea, sickle cell anemia, prematurity, D.M, and family history of malignant hyperthermia.
* Laparoscopic, endoscopic or abdominal surgeries.
* History of cardiac arrhythmia or palpitation.
* Patients with congenital heart, significant cardiovascular, respiratory diseases, renal impairment, hepatic dysfunction, hypo/hyperthyroidism or active peptic ulcer disease.
* Patients with neurological, psychiatric diseases, cognitive dysfunction, epilepsy or history of convulsions.
* Current treatment with xanthines or patient received aminophylline in the previous 24 hr. Hypersensitivity to aminophylline or other methylxanthines.
* Patients who need alteration in the sevoflurane concentration due to either hypo/hypertension were excluded from the study and replaced.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
4 Years
Maximum Age:
12 Years
Study:
NCT07011134
Study Brief:
Protocol Section:
NCT07011134