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Perioperative Hemodynamic Optimization Using the Photoplethysmography in Colorectal Surgery

Perioperative Hemodynamic Optimization Using the Photoplethysmography in Colorectal Surgery : A Randomized Controlled Study

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02343601
Acronym
PANEX3
Enrollment
160
Registered
2015-01-22
Start date
2014-12-01
Completion date
2016-12-01
Last updated
2026-04-02

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

Conditions

Polyp of Large Intestine, Colorectal Neoplasms, Crohn Disease

Brief summary

The purpose of this study is to determine whether hemodynamic optimization with photoplethysmography (ClearSight, Edwards Lifesciences, Irvine, CA) during colorectal surgery could decrease the incidence of perioperative complications.

Detailed description

All patients received the photoplethysmography monitoring, but the monitor was blinded in the control group.

Interventions

Use Photoplethysmography for hemodynamic optimization during colorectal perioperative period

Sponsors

University Hospital, Caen
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 95 Years
Healthy volunteers
No

Inclusion criteria

* Age\> 18 years * Colorectal surgery

Exclusion criteria

* Pregnant women * Black skin * Chronic renal insufficiency (MDRD \<30 ml/min)

Design outcomes

Primary

MeasureTime frameDescription
Incidence of patients presenting at least one complication after colorectal surgeryUp to 28 days after surgery (length of hospital stay)Two independent experts defined the presence of complication using an a priori classification.

Secondary

MeasureTime frame
All complications happening after colorectal surgeryUp to 28 days after surgery (length of hospital stay)
Real length of hospital stayUp to 28 days after surgery (length of hospital stay)
Perioperative mortality28 days after surgery

Countries

France

Contacts

PRINCIPAL_INVESTIGATORAnne-Lise Fiant, MD

University Hospital of Caen

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 3, 2026