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Comparison between two different techniques of fluid management after major abdominal surgeries

Postoperative fluid management after major abdominal surgery: Goal directed therapy versus Ultrasound guided volume assessment - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/01/079605
Enrollment
92
Registered
2025-01-28
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

None listed

Interventions

Intervention1: Ultrasound guided volume assessment comparator agent here is 2D ultrasound: Post operative monitoring of fluid status of patients using point of care ultrasound to assess venous conges

Sponsors

Institute of Post Graduation Medical Education and Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients aged between 18 to 60 years, all genders, ASA physical status I and II with no associated comorbidities, having no surgical complications within the study period and no sepsis or cardiogenic shock

Exclusion criteria

Exclusion criteria: Patients refuse to give consent, patients having known cardiac and respiratory disorders, contraindications or inability to initiate indwelling catheters, patients with major intra operative hemodynamic or cardiac events, patients requiring elective or emergency post operative ventilation

Design outcomes

Primary

MeasureTime frame
Point of Care Ultrasound and VExUS scoring will be a more sensitive tool to detect fluid responsiveness and early overload in postsurgical patientsTimepoint: 72 hours postoperatively

Secondary

MeasureTime frame
Assessment of hypoperfusion or fluid overload eventsTimepoint: 72 hours postoperatively;Requirement of vasopressors and diuretics to achieve perfusion goalsTimepoint: 72 hours postoperatively;Incidence of organ dysfunction such as lung congestion, AKI, ileus and altered liver function all attributed to perfusion pressure mismatchTimepoint: 72 hours postoperatively

Countries

India

Contacts

Public ContactArpan Chakraborty

Institute of Post Graduation Medical Education and Research,Kolkata

g.tapas@gmail.com9903745071

Outcome results

None listed

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