Laryngospasm

2

Review clinical trials related to Laryngospasm. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Perioperative Respiratory Adverse Events in Cleft Lip and Palate Surgery: Incidence, Risk Factors, and Clinical Scoring

Cleft lip and palate surgeries present unique anesthetic challenges due to shared airway access with the surgical field, frequent anatomical abnormalities, and a predominantly infant and toddler population. These factors substantially increase the risk of perioperative respiratory adverse events (PRAEs), including laryngospasm, bronchospasm, desaturation, post-extubation stridor, and unanticipated re-intubation. This prospective single-center observational cohort study aims to determine the true incidence of PRAEs in pediatric patients undergoing elective cleft lip and/or palate repair under general anesthesia, and to identify independent predictive risk factors using standardized airway assessment tools including the Han Mask Ventilation Score and the Intubation Difficulty Score (IDS). No interventions beyond routine clinical practice will be applied. All airway management decisions will remain at the discretion of the attending anesthesiologist.

Participants needed: 150
Trial details
Age: 0-3Biological sex: AllType: ObservationalSponsor: Marmara University Pendik Training and Research HospitalUpdated: Jun 16, 2026
Eligibility criteria

Age 0-3 years (infants and toddlers) [+3]

Pre-existing respiratory failure or active tracheostomy [+2]

Status: Not yet recruiting

Manual Valsalva Maneuver As a Preventive Measure of Postoperative Laryngospasm in Laryngomalacia Cases Undergoing Supraglottoplasty

We hypothesized that manual valsalva maneuver prevent incidence of postoperative laryngospasm after supraglottoplasty for cases of congenital laryngomalacia. Primary outcome: Incidence of postoperative stridor and laryngospasm Secondary outcome: incidence of reintubation, postoperative hemodynamics, duration of postoperative ICU and hospital stay

Participants needed: 58
Trial details
Age: 1-6Biological sex: AllType: InterventionalSponsor: Sameh FathyUpdated: Oct 4, 2024
Eligibility criteria

Infants and children ASA I or II aging from 1 month age - 6 years undergoing sup...

Parents refusal. [+2]