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COMPLETED
NCT07853547
NA

Controlled Ventilation During Anesthetic Emergence

Sponsor: King Abdulaziz Medical City

View on ClinicalTrials.gov

Summary

Absolutely - for a \*\*ClinicalTrials.gov-style Brief Summary\*\*, I'd keep it simple and patient-friendly like your example: The goal of this clinical trial is to learn whether maintaining controlled mechanical ventilation during emergence from general anesthesia can improve the quality and safety of recovery compared with conventional supported weaning in adults undergoing surgery with a breathing tube. The main questions it aims to answer are: * Does controlled mechanical ventilation during emergence reduce coughing and the duration of coughing before removal of the breathing tube? * Does it reduce agitation during emergence from anesthesia? * Does it reduce the need for breathing support, such as continuous positive airway pressure (CPAP), after removal of the breathing tube? * Are there differences in oxygen levels, blood pressure, heart rate, airway complications, or the time required for removal of the breathing tube? Researchers will compare controlled mechanical ventilation with conventional supported weaning during emergence from general anesthesia. Participants will: * Receive general anesthesia with a breathing tube for their planned surgery * Be assigned to either controlled mechanical ventilation or conventional supported weaning during emergence from anesthesia * Have their coughing, agitation, oxygen levels, blood pressure, heart rate, and airway-related events monitored during emergence * Have the time to removal of the breathing tube and any need for additional breathing support recorded This version is deliberately written in \*\*plain language rather than manuscript language\*\*, which is much closer to what ClinicalTrials.gov expects for the brief summary.

Official title: Controlled Mechanical Ventilation During Emergence From General Anesthesia Versus Conventional Supported Weaning for Awake Extubation: a Prospective, Randomized, Open-label, Parallel-group Clinical Trial

Key Details

Gender

All

Age Range

18 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

76

Start Date

2024-08-17

Completion Date

2025-03-16

Last Updated

2026-10-01

Healthy Volunteers

Yes

Interventions

DEVICE

Controlled/Full-Support Mechanical Ventilation During Emergence

Participants assigned to the intervention arm were maintained on controlled or full-support mechanical ventilation during emergence from general anesthesia rather than transitioning to conventional supported or spontaneous weaning. Ventilation modes included pressure-controlled ventilation (PCV), pressure-controlled ventilation-volume guaranteed (PCV-VG), synchronized intermittent mandatory ventilation (SIMV), and volume-controlled ventilation (VCV), with a target respiratory rate of 12 to 16 breaths per minute. Fresh gas flow was maintained at 10 to 15 L/min until end-tidal sevoflurane reached approximately 0.2 percent. Extubation was performed when the train-of-four ratio was at least 0.9, BIS or Entropy was 80 to 100, the participant opened the eyes in response to being called by name, and the attending anesthesiologist judged awake extubation to be appropriate.

Locations (1)

king Abdulaziz Medical City

Riyadh, Saudi Arabia