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The Impact of Pressure-Controlled Ventilation versus Volume-Controlled Ventilation on Surgical Field Visualization and Perioperative Respiratory Outcomes in Elderly Patients Undergoing UBE Surgery

The Impact of Pressure-Controlled Ventilation versus Volume-Controlled Ventilation on Surgical Field Visualization and Perioperative Respiratory Outcomes in Elderly Patients Undergoing UBE Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600118531
Enrollment
Unknown
Registered
2026-02-06
Start date
2026-03-01
Completion date
Unknown
Last updated
2026-02-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Elderly UBE surgery patient

Interventions

pressure-controlled ventilation group (PCV):?"After positioning in the prone position, the PCV group was ventilated with the peak inspiratory pressure (PIP) adjusted (maximum = 35 cmH?O) to maintain a
volume-controlled ventilation group (VCV):The VCV group was ventilated with a tidal volume (VT) of 6-8 ml/kg (based on ideal body weight), a respiratory rate (RR) of 10-16 breaths/min, 5 cmH?O of PEEP

Sponsors

the 925th Hospital, Joint Logistics Support Force, People's Liberation Army
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 85 Years

Inclusion criteria

Inclusion criteria: Patients aged 60 to 85 years, with a body mass index (BMI) between 18 and 32 kg/m², scheduled for elective unilateral biportal endoscopic (UBE) surgery under general anesthesia, with an anticipated surgical duration of 2 to 6 hours, and classified as American Society of Anesthesiologists (ASA) Physical Status I, II, or III.

Exclusion criteria

Exclusion criteria: Those who have severe infection, severe dysfunction of major organs, have had an upper respiratory tract infection or lung infection within the past two weeks or are in the acute exacerbation phase of lung disease, have intraoperative blood loss exceeding 1000ml, have been transferred to the ICU after surgery, have failed to complete all information collection, or are unwilling to participate in this study.

Design outcomes

Primary

MeasureTime frame
surgical field visualization score;postoperative pulmonary complications;

Secondary

MeasureTime frame
arterial blood gas? ;peak airway pressure?;plateau airway pressure?;tidal volume;blood pressure;heart rate;

Countries

China

Contacts

Public ContactWang Mei

the 925th Hospital, Joint Logistics Support Force, People's Liberation Army

wangmeiqjt@126.com+86 177 8592 3027

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 15, 2026