Determining Optimal Preload Volume using Point of Care Ultrasonography to Prevent Post Spinal Anaesthesia Hypotension

Determining Preload Volume using Point of Care Ultrasonography to Prevent Post Spinal Anaesthesia Hypotension- A Randomized Control Trail - Nil

Status

Active, not recruiting

Phases

Phase 4

Study type

Observational

Source

CTRI

Registry ID

CTRI/2024/10/074558

Enrollment

Registered

2024-10-01

Start date

Unknown

Completion date

Unknown

Last updated

2024-10-14

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: NIL

Eligibility

Inclusion criteria

Inclusion criteria: 18 to 60 years of age ASA Grade I and II Surgery not lasting for more than 3 hours

Exclusion criteria

Exclusion criteria: Emergency Surgeries Under general anesthesia Neurologic disorders Cardiac Anomalies

Design outcomes

Primary

Measure	Time frame
Primary objective of the study will be to assess the episodes of hypotension (hypotension defined as MAP =80% of the baseline or MAP =60mmhg)Timepoint: It will be assessed every 5 minutes after giving spinal anaesthesia for the first 40 minutes	—

Secondary

Measure	Time frame
Secondary objective will be calculating the amount of vasopressor used and total intraoperative fluid givenTimepoint: At the end of first hour of surgery	—

Countries

India

Contacts

Public ContactDr Chaitanya Kamat

J N Medical College, Belagavi

drchaitanya12@gmail.com8150038305

Outcome results

None listed

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