Surgeon-Anesthesiologist Collaboration

Pheochromocytoma Clinical Trial

— CCAP  

Official title:

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

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT03158870
• Other study ID #: 69HCL17_0030
• Status: Not yet recruiting
• Phase: N/A
• First received: May 17, 2017
• Last updated: May 17, 2017
• Start date: July 2017
• Est. completion date: December 2017

Study information

• Verified date: May 2017
• Source: Hospices Civils de Lyon
• Contact: Jean-Christophe LIFANTE, MD, PhD
• Phone: 04 78 56 90 95
• Email: jean-christophe.lifante[@]chu-lyon.fr
• Is FDA regulated: No
• Study type: Observational

Clinical Trial 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.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 1122
• Est. completion date: December 2017
• Est. primary completion date: December 2017
• Gender: All
• Age group: 18 Years and older

Eligibility

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

Related Conditions & MeSH terms

• Collaboration
• Pheochromocytoma

Intervention

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

Locations

Country	Name	City	State
France	Pôle Information Médicale Evaluation Recherche des Hospices Civils de Lyon - Centre Hospitalier Lyon Sud	Pierre-Bénite

Sponsors (1)

Lead Sponsor	Collaborator
Hospices Civils de Lyon

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Presence of an intraoperative hemodynamic instability	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	At the time of surgery (less than 4 hours)