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A prospective observational study of pain assessment after operation for planned cancer surgery

Utility of Perfusion index as a tool for assessment of Acute postoperative pain in elective oncosurgery: A PROSPECTIVE OBSERVATIONAL STUDY - NA

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2023/09/057736
Enrollment
84
Registered
2023-09-15
Start date
Unknown
Completion date
Unknown
Last updated
2023-10-16

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 Health Condition 2: D499- Neoplasm of unspecified behavior of unspecified site Health Condition 3: R52- Pain, unspecified

Interventions

Intervention1: NA: NA

Sponsors

Tata Memorial Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Adults : Age 18–80 years 2. ASA 1 and 2 3. Patients posted for surface surgeries which include ,breast surgery ( without reconstruction) , orthopedic surgeries ,head and neck surgeries awake , non intubated patient

Exclusion criteria

Exclusion criteria: 1. Severe cardiac disease (ischemic/valvular/failure related) which limit the functional activities of the patient, (above NYHA class 1) 2. History of chronic kidney disease, or current deranged renal functions, 3. History of liver disease, or current deranged liver functions, 4. Patients on preoperative opioids, both strong and weak opioids like Tramadol, codeine. 5. Patients with a history of a neurological, psychiatric, disorder, who were taking psychotropic drugs 6. Patients with allergy to any drug used in the study. 7. Postoperative unstable hemodynamic status, or on ventilator support 8. Patient who have received intraoperative regional analgesia (Epidural/regional blocks) 9. Patients on anti hypertensive(NTG ) / Dexmedetomidine infusion 10. Patients with blood loss more than 1 litre. 11. Postoperative temperature less than 35 degree Celsius or 95 F 12. Surgeries which lasted for more than 3 hours

Design outcomes

Primary

MeasureTime frame
To establish correlation between NRS score and PI or delta PI in PACU patients undergoing surface surgeries at a tertiary cancer care hospital. To analyse the trend of perfusion index with pain scoreTimepoint: The PI will be recorded every 30 mins after admission to recovery room at the time of the first request for analgesia At the time of the first request for analgesia NRS for pain intensity will be recorded

Secondary

MeasureTime frame
- To analyse the trend of perfusion index with pain scoreTimepoint: Thirty minutes after postoperative analgesia, second measurements of the above-mentioned parameters will be taken simultaneously. (NRS for pain intensity, PI, HR, MAP, peripheral oxygen saturation, & axillary temperature.)

Countries

India

Contacts

Public ContactDr Siddharaj Vaze

Tata memorial hospital

sidvaze@gmail.com9869937199

Outcome results

None listed

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