The study to show factors affecting early recovery after surgery including fluid management

â??A randomised prospective study to compare the implementation of SGPGI enhanced recovery program(SERP) including goal directed fluid therapy Vs. standard therapy in major abdominal surgeriesâ??

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2020/03/024318

Enrollment

Registered

2020-03-27

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

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

Conditions

Health Condition 1: K918- Other intraoperative and postprocedural complications and disorders of digestive system

Interventions

Intervention1: SVV Guided GDT Group: Fluid will be given acc. to SVV using FLOTRAC SYSTEM. normal SVV 10-12 (maintained by 1-2 ml/kg/hr) if more then 12 then 200ml fluid bolus will be given and SVV

Eligibility

Inclusion criteria

Inclusion criteria: Patients willing to participate Pt age: > 18 yrs and found fit for major abdominal surgery ASA 1 and 2 Patients undergoing major abdominal surgeries including Whippleâ??s procedure Colorectal surgeries

Exclusion criteria

Exclusion criteria: Patientâ??s refusal to participate Patients with severe, persistent peripheral vasoconstriction or arterial spasm, such as in shock states Device related exclusion criteria : Patients of dilated cardiomyopathy with left ventricular ejection fraction less than 40% Patients with artificial hearts and ventricular assist devices (VAD). Patients with severe, persistent arrhythmias

Design outcomes

Primary

Measure	Time frame
To study and compare the postoperative length of stay in postop ICU in SGPGI Early Recovery Program (SERP) group utilising goal directed fluid therapy (by FloTrac/Vigileo ,SVV guided fluid therapy ) with standard therapy group utilising CVP based intraoperative fluid management.Timepoint: 24 hrs	—

Secondary

Measure	Time frame
To study and compare the intraoperative fluid requirement in the SERP(SVV) and standard therapy group(CVP). (total fluid given, bolus given, ml/kg body wt. fluid in both groups). To compare the intraoperative hemodynamics in both group. To compare the pain scores with Visual Analogue Scale (VAS) in both groups. Incidence of nausea and vomiting in both groups. To Study the adverse perioperative events and complications. Timepoint: 24 hrs	—

Measure

Time frame

To study and compare the intraoperative fluid requirement in the SERP(SVV) and standard therapy group(CVP). (total fluid given, bolus given, ml/kg body wt. fluid in both groups). To compare the intraoperative hemodynamics in both group. To compare the pain scores with Visual Analogue Scale (VAS) in both groups. Incidence of nausea and vomiting in both groups. To Study the adverse perioperative events and complications. Timepoint: 24 hrs

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Countries

India

Contacts

Public ContactDr Pratibha Yadav

SGPGI

drsandeepsahu09@gmail.com8004904598

Outcome results

None listed

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