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Evaluation of Respiratory Mechanics in Supine and PARK-bench Positions (SPARK)

Evaluation of Respiratory Mechanics in Supine and PARK-bench Positions in Patients Undergoing Elective Neurosurgery: a Cross-over Physiological Study

Status
Enrolling by invitation
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06448988
Acronym
SPARK
Enrollment
22
Registered
2024-06-07
Start date
2024-06-06
Completion date
2025-07-31
Last updated
2024-10-23

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

Conditions

Ventilation Therapy; Complications, Ventilator-Induced Lung Injury

Brief summary

The primary objective of this prospective observational physiological study is to evaluate the variation in regional distribution of intrapulmonary volume in the dependent and non-dependent lung regions in patients undergoing neurosurgical intervention between supine and Park-Bench position.

Detailed description

The Park-Bench position is a variant of the lateral position used in neurosurgical interventions where lesions of the posterior cranial fossa and ponto-cerebellar angle need to be approached. The patient is placed in a lateral-oblique position with the arm on the side they are lying on extending out of the operating bed and supported by an external support. The head is fixed in flexion and rotation with the Mayfield headrest immobilizing the head, allowing exposure of the surgical region of interest. In the lateral decubitus position, several factors contribute to changing respiratory mechanics: airway resistance increases and compliance decreases. Furthermore, the gravitational gradient is altered, which is one of the main factors in the regional distribution of intrapulmonary air volume and tidal volume distribution: the phenomenon of overdistension of the non-dependent lung and collapse of the dependent lung could occur. Fully understanding these physiological changes could optimize mechanical ventilation settings and thus avoid causing damage to lung parenchyma (Ventilator-Induced Lung Injury). The primary hypothesis of this physiological study is to evaluate changes in regional distribution of intrapulmonary volume when transitioning from the supine position to the Park-Bench position.

Interventions

OTHERPark Bench position

To evaluate, during the procedure, the variation in regional distribution of intrapulmonary volume in the dependent and non-dependent lung regions in patients undergoing neurosurgical intervention between supine and Park-Bench position.

Sponsors

Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Lead SponsorOTHER

Study design

Observational model
CASE_CROSSOVER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age \>18 * Patients scheduled for elective neurosurgery in Park-Bench position.

Exclusion criteria

* Age \< 18 * BMI \> 30 kg/m2 * Obstructive or restrictive lung disease with oxygen supplementation * Pacemaker * Pregnancy * Absence of history of pulmonary embolism, thoracic surgery or chest wall abnormalities, organ transplant, lung metastases * New York Heart Association \>2 or hemodynamic instability (Mean Arterial Pressure\<60mHg)

Design outcomes

Primary

MeasureTime frameDescription
Variation in tidal volume distribution in the dependent and non-dependent lung during neurosurgical intervention, from supine to Park Bench position.Variation, during the procedure, in tidal volume distribution in the dependent and non-dependent lung during neurosurgical intervention, from supine to Park Bench position.Variation in tidal volume distribution in the dependent and non-dependent lung during neurosurgical intervention, from supine to Park Bench position.

Secondary

MeasureTime frameDescription
Airway closure incidence in the supine and Park Bench positionAirway closure incidence, during the procedure, in the supine and Park Bench positionAirway closure incidence in the supine and Park Bench position

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026