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comparison of pain monitors ANI and SPI in supratentorial tumour surgery

Evaluating nociceptive indices ANI and SPI In supratentorial tumour excisionn under general anaesthesia -a prospective single group correlational study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2018/02/012170
Enrollment
70
Registered
2018-02-26
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: C71- Malignant neoplasm of brain Health Condition 2: null- supra tentorial tumour resction under general anaesthesia

Interventions

None listed

Sponsors

Nimhans
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: elective supratentorial tumour resection under GA electively

Exclusion criteria

Exclusion criteria: Age less than 18yrs Emergency surgery Patients on beta blockers ,calcium channel blockers Patients with autonomic dysfunction, thyroid dysfunction Patients with peripheral vascular disease Patients with HB less than 11g/dl Patient requiring major blood transfusion more than 50% blood volume. BMI more than 35 Patients with significant organ system dysfunction Intraoperative hemodynamic instability ;defined as a fall in blood pressure by 30% of baseline Patients requiring inotropic and vasopressor infusion

Design outcomes

Primary

MeasureTime frame
Evaluating the changes in SPI and ANI with changes in HR and MAP at predefined time pointsTimepoint: asessed at end of data aquisiotion period of 14-18 months

Secondary

MeasureTime frame
Evaluating the changes in SPI and ANI with changes in HR and MAP at predefined stimulus timesTimepoint: at end of study;Evaluating the numerical pain score at the end of one hour following the completion of surgery and evaluating the correlation of the numerical pain score with ANI and SPI at one hour post surgery.Timepoint: end of study;To evaluate the change in SPI and ANI independently at all these time points of surgical stimulation.Timepoint: at end of study

Countries

India

Contacts

Public ContactPrashanth A Menon

NIMHANS Bangalore

krmsr2000@yahoo.com9742341452

Outcome results

None listed

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