Mobile based application for prediction of spinal anaesthesia hypotension

Evaluation of an application to predict subarachnoid block induced hypotension by using clinical and radiological patient parameters. - Nil

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/04/084257

Enrollment

Registered

2025-04-07

Start date

Unknown

Completion date

Unknown

Last updated

2025-04-28

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: Using Mobile based application: In this group, mobile based application is used to analyse and predict the incidence of post spinal hypotension. The total duration of intervention is du

Eligibility

Inclusion criteria

Inclusion criteria: Patients of ASA 1 and 2 undergoing elective surgery under spinal anaesthesia

Exclusion criteria

Exclusion criteria: Patients other than ASA 1 and 2. Pregnant patients.

Design outcomes

Primary

Measure	Time frame
The primary outcome of the study is to evaluate the efficacy of the application in predicting subarachnoid block induced hypotensionTimepoint: 5 mins after spinal anesthesia	—

Secondary

Measure	Time frame
The secondary outcome of the study is to assess the clinical decision making & patient outcome.Timepoint: 5 mins after spinal anaesthesia, intraoperative period, immediate postoperative period	—

Countries

India

Contacts

Public ContactAshok Kumar B

Saveetha Medical college

drmbashok@rocketmail.com9003026194

Outcome results

None listed

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