Skip to content

A comparison of Hemodynamic changes in patients undergoing cesarean section when pre loaded with Crystalloid and Colloid.

A Study to Compare the Hemodynamic Changes in Patients Undergoing Cesarean Section under Spinal Anaesthesia When Pre-Loaded With Crystalloid vs. Colloid. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/01/079818
Enrollment
70
Registered
2025-01-31
Start date
Unknown
Completion date
Unknown
Last updated
2025-03-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O94-O9A- Other obstetric conditions, not elsewhere classified

Interventions

Intervention1: Inj. RL intravenously at the rate of 10ml/kg.: Patient will be preloaded with 10ml/kg of ringer lactate solution over a period of 20 minutes just prior to the administration of final a

Sponsors

Smt Bhikiben Kanjibhai Shah Medical Institute and Research Center
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)The patients belonging to ASA-I and ASA-II. 2)Age Group from 18 to 35 years. 3)Patients undergoing LSCS. 4)Duration of surgery from 2 to 2.5 hours.

Exclusion criteria

Exclusion criteria: A)All contraindications for spinal anaesthesia like: Patients refusal Local infections Spinal deformities Bleeding disorders Increased intracranial tension Systolic blood pressure less than 100mmHg. B)Age less than 18 years or more than 60 years. C)Concomitant diseases – diabetes mellitus, hypertension, heart diseases, obesity. D)Patients other than ASA-I and ASA-II.

Design outcomes

Primary

MeasureTime frame
This study will help us to know that which out of two intravenous solutions Colloid or Crystalloid is a better preloading solution to achieve the stable hemodynamics during cesarean sectionTimepoint: Heart rate ,Systolic and diastolic blood pressure and mean arterial pressure will be monitored every 2 minutes for the first 10 minutes and then every 5 minutes till the next hour and then every 15 minutes till the end of surgery

Secondary

MeasureTime frame
Requirement of vasopressor.Incidence of nausea and vomiting.Incidence if allergic reactions Timepoint: monitored every 2 minutes for the first 10 minutes and then every 5 minutes till the next hour and then every 15 minutes till the end of surgery

Countries

India

Contacts

Public ContactDr Priya Kishnani

Smt. Bhikiben Kanjibhai Shah Medical Institute and Research Centre

drpriya0809@gmail.com9898076139

Outcome results

None listed

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