FindTrial
Sign In

A study to evaluate perfusion index for monitoring of depth of anaesthesia in adults.

Correlation between perfusion index and Bispectral index for depth of anaesthesia monitoring in adult patients undergoing elective surgery under General Anaesthesia: An Observational Study - nil

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/10/075658
Enrollment
40
Registered
2024-10-23
Start date
Unknown
Completion date
Unknown
Last updated
2024-12-09

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: After administration of general anaesthesia as per protocol, simultaneously the value of perfusion index value and BiSpecral index at different timestamps will be recorded. Control

Sponsors

Dr Roshan Andleeb
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. ASA I-II patients of either sex 2. Age 18-50 years 3. Patients undergoing elective surgery under general anaesthesia. 4. Surgical procedures with short operative times, minimal tissue trauma, and minimal intraoperative fluid shift 5. body mass index (BMI) 18–39 kg/m2

Exclusion criteria

Exclusion criteria: 1. Patients with allergies to anaesthesia drugs 2. Patient with peripheral vascular disease, significant cardiac, renal, pulmonary, hepatic, neurological and cerebrovascular disease. 3. Patients with a history of brain injury 4. Patients on psychiatric medication

Design outcomes

Primary

MeasureTime frame
To determine the correlation between perfusion index (PI) and Bispectral Index (BIS) during anaesthesia, and to compare the predictive accuracy of PI and BIS for anaesthesia depth monitoring Timepoint: intraoperative period—

Secondary

MeasureTime frame
To evaluate the association between PI and hemodynamic parameters during anaesthesia. To evaluate the correlation between PI and the MAC value during anaesthesia To evaluate the association between PI and other parameters such as opioid usage, intraoperative fluid requirement, propofol usage, and blood loss. Timepoint: intraoperative period—

Countries

India

Contacts

Public ContactDr Roshan Andleeb

AIIMS Kalyani

roshan8978@gmail.com09045292647

Outcome results

None listed

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