Assessing intraoperative pain using analgesia nociception index during neurosurgery

Evaluation of Analgesia Nociception Index monitor in managing intraoperative pain during neurosurgery - nil

Status

Active, not recruiting

Phases

Phase 3Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2018/01/011299

Enrollment

Registered

2018-01-12

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- Undergoing neurosurgery for brain tumors

Interventions

Intervention1: Pin site and incision site local anaesthetic infiltration: All patients in this group will receive local anesthetic infiltration at pin and incision site Control Intervention1: Scalp bl

Eligibility

Inclusion criteria

Inclusion criteria: undergoing elective supra-tentorial craniotomy for brain tumors

Exclusion criteria

Exclusion criteria: diabetes mellitus, systemic hypertension, significant arrhythmias, chronic pain, cerebro-vascular disease, allergy to local anesthetic drugs, coagulopathy, scalp infection, prior craniotomy, pacemaker in-situ, or pregnancy

Design outcomes

Primary

Measure	Time frame
fentanyl consumptionTimepoint: Intraoperative period	—

Secondary

Measure	Time frame
NRSTimepoint: Post extubation	—

Countries

India

Contacts

Public ContactKaushic A

National Institute of Mental Health and Neurosciences

krmsr2000@yahoo.com918026995415

Outcome results

None listed

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