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NCT02989415: AVATaR
Assessment of Ventilatory Management During General Anesthesia for Robotic Surgery
trial testing Mechanical Ventilation in Robotic Surgery in 1,015 participants. Completed in 15 January 2020.
15 March 2019
Quick facts
| Lead sponsor | Hospital Israelita Albert Einstein |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 1,015 |
| Start date | 3 August 2017 |
| Primary completion | 15 March 2019 |
| Estimated completion | 15 January 2020 |
| Sites | 12 locations across Belgium, Israel, Germany, Spain, United States, Brazil |
Drugs / interventions tested
- Mechanical Ventilation
Conditions studied
- Robotic Surgery — all drugs for Robotic Surgery →
- Mechanical Ventilation — all drugs for Mechanical Ventilation →
Sponsor
Hospital Israelita Albert Einstein
Who can join
18 and older, any sex, with Robotic Surgery or Mechanical Ventilation. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The aim of this study is to assess the incidence of postoperative pulmonary complications in patients undergoing mechanical ventilation during general anesthesia for robotic surgery, to characterize current practices of mechanical ventilation and to evaluate a possible association between ventilatory parameters and postoperative pulmonary complications.
Publications & conference data
5 peer-reviewed publications reference this trial (live from Europe PMC):
-
Epidemiology, practice of ventilation and outcome for patients at increased risk of postoperative pulmonary complications: LAS VEGAS - an observational study in 29 countries.
LAS VEGAS investigators. · · 2017 · cited 203× · PMID 28633157 · DOI 10.1097/eja.0000000000000646 -
Ventilation and outcomes following robotic-assisted abdominal surgery: an international, multicentre observational study.
Assessment of Ventilation during general AnesThesia for Robotic surgery (AVATaR) Study Investigators, PROtective VEntilation (PROVE) Network, Writing Committee Members, Steering Committee Members, et al · · 2021 · cited 15× · PMID 33131757 · DOI 10.1016/j.bja.2020.08.058 -
International multicenter observational study on assessment of ventilatory management during general anaesthesia for robotic surgery and its effects on postoperative pulmonary complication (AVATaR): study protocol and statistical analysis plan.
Queiroz VNF, da Costa LGV, Barbosa RP, Takaoka F, et al · · 2018 · cited 4× · PMID 30139899 · DOI 10.1136/bmjopen-2018-021643 -
Risk factors for PPCs in laparoscopic non-robotic vs. laparoscopic robotic abdominal surgery (LapRas): rationale and protocol for a patient-level analysis of LAS VEGAS and AVATaR.
Serafini SC, Hemmes SNT, Serpa Neto A, Schultz MJ, et al · · 2024 · cited 1× · PMID 38987020 · DOI 10.1016/j.redare.2024.07.001 -
The PROtective VEntilation (PROVE) Network - advancing research and collaboration in mechanical ventilation.
Schultz MJ, Ball L, Bernardi M, Battaglini D, et al · · 2025 · PMID 40929471 · DOI 10.62675/2965-2774.20250399
Verify or expand the search:
- PubMed search for NCT02989415
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
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Trials testing the same drug.
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- NCT04241874 — PEEP and Spontaneous Breathing During ARDS · NA · completed
- NCT04026451 — Spectral Edge Frequency From Spectral EEG Analysis to Guide Deep Sedation in the Critical Care Setting (Pilot) · NA · withdrawn
- NCT03401736 — The Diversity of Intestinal Microbiota in Patients With Different Sedative-hypnotics Undergoing Mechanical Ventilation · NA · withdrawn
Other recruiting trials for Robotic Surgery
Currently open trials in the same condition.
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Other Hospital Israelita Albert Einstein trials
Trials by the same sponsor.
- NCT07447674 — ED Post-Discharge Digital Follow-Up: A Communication Comparison · NA · not yet recruiting
- NCT07398222 — Gastric Content in Fasting Volunteers and in Tirzepatide Users: an Observational and Cross-sectional Study · recruiting
- NCT07233837 — Hydrogen Peroxide and Ultraviolet Light for Disinfecting Surfaces in Intensive Care Units · NA · recruiting
- NCT06726707 — COPPER: A Trial Evaluating Copper-based Products for Incontinence-associated Dermatitis · Phase 2, PHASE3 · withdrawn
- NCT07112846 — Prospective Clinical Registry for Evaluation of Exanthematous Infections and Coinfections · not yet recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT02989415 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Hospital Israelita Albert Einstein
- Last refreshed: 12 February 2020
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02989415.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing