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Comparison of three pain assessment methods for detecting pain in mechanically ventilated patients after surgery in the intensive care unit.

Comparison of Critical Care Pain Observation Tool, Behavioral Pain Scale and Non-verbal Pain Scale for Pain Assessment in Mechanically Ventilated Post Surgical ICU Patients : A Prospective Observational Study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/03/106675
Enrollment
106
Registered
2026-03-20
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Nil: Nil

Sponsors

Sir Ganga Ram Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Post operative patients admitted to ICU and mechanically ventilated for 24 hrs. 2.Adult patients both males and female 18 years of age or more. 3.Hemodynamically stable at assessment time 4.Ramsay sedation scale 4 and 5

Exclusion criteria

Exclusion criteria: 1. Patients with quadriplegia, use of neuromuscular blocking agents, presence of peripheral neuropathy 2.Morbidly obese (BMI greater than 40), pregnancy, left ventricular ejection fraction less than 25%. 3.Patients with ongoing treatment for chronic pain, pre-existing psychiatric or neurological issues. 4.Family members of eligible patients not willing to participate in the study. 5.Ramsay sedation scale greater than 5. 6.Patients given breakthrough analgesia or sedation during the assessment. 7.Patients receiving drugs likely to blunt or distort heart rate and blood pressure responses to nociceptive stimuli

Design outcomes

Primary

MeasureTime frame
Scores assessed by various behavioral pain tools (CPOT, BPS and NVPS) in response to a nociceptive procedure as determined by changes in physiological parameter (HR/MAP)Timepoint: Baseline rest, during nociceptive procedures, and 20 minutes after completion of the procedure.

Secondary

MeasureTime frame
Change in individual behavioral component scores within CPOT, BPS & NVPS in response to nociceptive proceduresTimepoint: Baseline rest, during nociceptive procedures & 20 minutes post-procedure.

Countries

India

Contacts

Public ContactDr Raj kumar A

Sir Ganga Ram Hospital

ddhar2001@gmail.com9811231261

Outcome results

None listed

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