Preoperative Anxiety Experienced by the Pediatric Patient

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Review clinical trials related to Preoperative Anxiety Experienced by the Pediatric Patient. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Evaluating Operation Calm With Children, Parents, and Clinicians

Operation Calm is a single-arm, mixed-methods feasibility study evaluating a virtual reality (VR) nature-based mindfulness intervention with children and adolescents aged 6-17 years, parents, and clinicians. Children complete one guided mindfulness session combining an immersive 360° nature environment with breathing, sensory awareness, and grounding exercises. Parents and clinicians view the intervention through a secure online link. The study examines feasibility, acceptability, engagement, usability, perceived usefulness, and child tolerability. It also explores immediate changes in children's anxiety, calmness, state mindfulness, and nature connectedness. Feedback from children, parents, and clinicians will guide further refinement of Operation Calm before it is evaluated in a larger clinical study.

Participants needed: 150
Trial details
Age: 6+Biological sex: AllType: InterventionalSponsor: McGill UniversityUpdated: Oct 7, 2026Locations: 1
Eligibility criteria

Aged 6-17 years [+14]

Unable to safely or comfortably use the VR headset [+7]

Status: Not yet recruiting

Children of Age 2-6years Undergoing Elective Surgery Will be Divided Into Two Groups Randomly. This Study Aims to Evaluate if Intranasal Dexmedetomidine is Better Than Intranasal Ketamine in Producing Sedation and Reducing Parent Separation Anxiety Before Surgery.

This study aims to compare intranasal dexmedetomidine versus intranasal ketamine as a premedication in children undergoing surgery in our population. Hypothesis is Intranal dexmedetomidine is better than intranasal ketamine in producing preoperative sedation in pediatric patients undergoing surgery under general anesthesia.

Participants needed: 60
Trial details
Phase: Phase 1, Phase 2Age: 2-6Biological sex: AllType: InterventionalSponsor: Liaquat National Hospital & Medical CollegeUpdated: Sep 18, 2025
Eligibility criteria

American society of Anesthesiologist (ASA) class-I and II [+1]

Known hypersensitivity to study drugs [+5]