FindTrial
Sign In

Observational and Minimal Interventional Study Designed to Collect Data During Planned Surgery

Prospective Observational and Interventional Study Designed to Collect Physiological Data During Elective Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2015/03/005657
Enrollment
75
Registered
2015-03-27
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Elective, Non-thoracic, Open surgical procedures

Interventions

None listed

Sponsors

Nellcor Puritan Bennett LLC Doing Business as Covidien
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: • Adult patient >= 18 years of age scheduled for an elective, open non-thoracic surgical procedure. • Expected duration of the surgical procedure to be >= 1.5 hours. • Expected radial artery cannulation and ECG monitoring in the Operating Room. • Measurement of Invasive Blood Pressure via Radial cannulation site

Exclusion criteria

Exclusion criteria: Patients with active cardiac arrhythmia, indwelling intra-aortic balloon pump, Left Ventricular assist device, undergoing thoracic open surgery, having history of severe contact allergies to adhesive material e.g. pulse oximetry sensors etc, skin lesions or deformities on fingers and forehead, pregnant female and vulnerable patients.

Design outcomes

Primary

MeasureTime frame
Not Applicable (data collection study)Timepoint: Not Applicable (data collection study)—

Secondary

MeasureTime frame
Not Applicable (data collection study)Timepoint: Not Applicable—

Countries

India

Contacts

Public ContactPartha Chatterjee

SIRO Clinpharm Pvt Ltd

partha.chatterjee@siroclinpharm.com022-61088000

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026