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Compliance-Guided Abdominal Wall Closure Strategy in Large Ventral Hernia Repair

Impact of a Compliance-Guided Intraoperative Abdominal Wall Closure Decision Strategy on Early Postoperative Respiratory Failure After Large Ventral Hernia Repair Following Preoperative Botulinum Toxin A

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07422441
Acronym
CLOSE-STAT
Enrollment
50
Registered
2026-02-20
Start date
2026-02-20
Completion date
2026-11-01
Last updated
2026-02-20

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

Conditions

Hernia Incisional, Hernia, Ventral, Postoperative Complications, Respiratory Insufficiency

Keywords

adbominal wall closure, static compliance, respiratory system compliance, intraoperative monitoring, intra-abdominal pressure, complex hernia repair, botulinum toxin a

Brief summary

People undergoing repair of large ventral hernias can develop breathing problems after surgery, especially around the time when the abdominal wall is closed. During closure, pressure inside the abdomen may increase and lung mechanics can worsen. This study will evaluate a structured intraoperative decision approach that uses standard anesthesia measurements of static respiratory system compliance at predefined timepoints to support the choice of abdominal wall closure technique. The main goal is to assess the rate of early postoperative respiratory failure within 72 hours after surgery.

Detailed description

This is a prospective, single-arm, decision-guided interventional study in adults undergoing elective repair of large ventral hernias after preoperative botulinum toxin A preparation as part of the local prehabilitation pathway. The study focuses on the intraoperative abdominal wall closure phase, when physiological changes may increase the risk of early postoperative respiratory complications. Mechanical ventilation is standardized during measurement timepoints using volume-controlled ventilation with tidal volume set to 6 mL per kg of ideal body weight and a positive end-expiratory pressure of 10 cmH2O. Full neuromuscular blockade is ensured to minimize measurement variability. Static respiratory system compliance is recorded at three predefined timepoints: after endotracheal intubation before skin incision (baseline), during abdominal wall closure (decision timepoint), and before extubation. The intraoperative decision strategy considers a closure physiologically tolerable when static compliance remains at least 70 percent of the baseline value. If compliance falls below this threshold at the closure decision timepoint, the surgical team considers avoiding tension closure and may use a bridging or alternative closure approach according to clinical judgment. When intra-abdominal pressure is measured as part of routine care, these values are recorded as an additional physiological parameter. Perioperative data are captured in a dedicated case report form, and patients are observed for early respiratory outcomes during the first 72 hours after surgery.

Interventions

OTHERCompliance-Guided Abdominal Wall Closure Decision Strategy

A predefined intraoperative decision strategy that uses standardized measurements of static respiratory system compliance (Cstat) during abdominal wall closure to support selection of closure technique, with a predefined physiological tolerance threshold based on the baseline measurement.

Sponsors

Swissmed Hospital
Lead SponsorOTHER
Medical University of Gdansk
CollaboratorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

Single-arm, decision-guided intraoperative closure strategy based on predefined static compliance measurements at three timepoints.

Eligibility

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

Inclusion criteria

* Age 18 years or older * Elective repair of a large ventral abdominal wall hernia (including incisional hernia) * Preoperative botulinum toxin A preparation performed as part of the local prehabilitation pathway * Preoperative abdominal CT available * General anesthesia with mechanical ventilation and feasibility of standardized intraoperative respiratory mechanics measurements

Exclusion criteria

* Severe preoperative respiratory failure judged to preclude standardized intraoperative respiratory mechanics assessment * Inability to obtain reliable static respiratory system compliance measurements at predefined timepoints * Hemodynamic instability preventing protocolized measurements (as judged by the anesthesiologist)

Design outcomes

Primary

MeasureTime frameDescription
Incidence of postoperative respiratory failure within 72 hoursWithin 72 hours after surgeryPercentage of participants who develop postoperative respiratory failure within 72 hours after surgery, defined as meeting ≥1 of the following criteria: * Reintubation for respiratory reasons; OR * Non-invasive ventilation (NIV) or high-flow nasal oxygen (HFNO) delivered for \>6 consecutive hours for respiratory reasons; OR * Escalation of respiratory support for respiratory reasons (e.g., increase in oxygen delivery device/flow/FiO₂ or ventilatory support level). Unit of measure / tool: % of participants (derived from routine clinical documentation: anesthesia record, PACU/ICU charts, respiratory therapy notes).

Secondary

MeasureTime frameDescription
Change in static respiratory system compliance from baseline to closure decisionIntraoperative (baseline to closure decision timepoint)Change in static respiratory system compliance (Cstat) from: * Baseline: after intubation, before incision to * Closure decision timepoint: immediately prior to the final abdominal wall closure strategy decision under standardized ventilation conditions. Unit of measure / tool: ΔCstat (mL/cmH₂O) measured/calculated from the mechanical ventilator using: * Cstat = VT / (Pplat - PEEP) (if you intend this exact formula, include it) * VT, Pplat, PEEP obtained from ventilator readings (anesthesia machine record)
Proportion of cases requiring change in abdominal wall closure strategyIntraoperative (during abdominal wall closure)Percentage of participants in whom the preoperatively planned tension closure is changed at the closure decision timepoint to: * bridging, or * another predefined alternative closure approach based on intraoperative physiological assessment per protocol. Unit of measure / tool: % of participants (surgeon operative report + intraoperative record; categorized closure strategy).
Intra-abdominal pressure during abdominal wall closureIntraoperative (at time of measurement)Intra-abdominal pressure (IAP) values recorded per routine care at prespecified intraoperative timepoints (as applicable in your workflow). If you want one summary statistic, specify it (recommended), e.g.: * Peak intraoperative IAP during closure, or * IAP at closure decision timepoint Unit of measure / tool: mmHg, measured using the site's routine IAP technique (e.g., bladder pressure via urinary catheter system) as documented in the anesthesia/ICU record.

Contacts

CONTACTMagdalena Halska
worldofsurge@gmail.com607870690
PRINCIPAL_INVESTIGATORIrmina Anna Śmietański, MD, PhD

Śmietański Hernia Center, LUX MED Hospital in Gdańsk

STUDY_CHAIRMaciej Śmietański, Prof.

Śmietański Hernia Center, LUX MED Hospital in Gdańsk

STUDY_DIRECTORMateusz Zamkowski, MD, PhD

Śmietański Hernia Center, LUX MED Hospital in Gdańsk

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 21, 2026