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Surgeon-Anesthesiologist Collaboration

Influence of Surgeon-anesthesiologist Collaboration on Patient Outcomes After Pheochromocytoma Surgery

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03158870
Acronym
CCAP
Enrollment
1122
Registered
2017-05-18
Start date
2017-07-31
Completion date
2017-12-31
Last updated
2017-05-18

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

Conditions

Collaboration, Pheochromocytoma

Brief summary

Collaboration between the surgeon and the anesthesiologist is key for delivering a safe pheochromocytoma surgery. This study aims to establish the collective performance of surgeon-anesthesiologist team by quantifying the relationship between their previous collaborations and patient complications.

Interventions

PROCEDURESurgery complications

Assessment of the influence of surgeon-anesthesiologist collaboration on surgery complications during and up to 30 days after pheochromocytoma surgery.

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* All patients who underwent surgical procedure for pheochromocytoma in 8 French university hospitals from January 2000 to December 2016

Exclusion criteria

* Age \< 18 years old * Patients operated for incidentaloma or with paraganglioma diagnosis

Design outcomes

Primary

MeasureTime frameDescription
Presence of an intraoperative hemodynamic instabilityAt the time of surgery (less than 4 hours)An intraoperative hemodynamic instability is defined as the occurrence of at least one intraoperative episode of systolic blood pressure ≥ 160 mmHg and at least one episode of mean blood pressure ≤ 60 mmHg

Countries

France

Contacts

Primary ContactJean-Christophe LIFANTE, MD, PhD
jean-christophe.lifante@chu-lyon.fr04 78 56 90 95
Backup ContactAntoine DUCLOS, MD, PhD
antoine.duclos@chu-lyon.fr04 72 11 51 66

Outcome results

None listed

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