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To compare the recovery of patients after controlled fluid management and applying faster recovery protocols during laparoscopic living donor kidney transplantation

A Randomised Prospective Study To Compare The Implementation Of SGPGI Enhanced Recovery Program And Goal Directed Fluid Therapy In Laparoscopic Donor Nephrectomy For Live Related Renal Transplantation - CERPGOLD

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/05/018871
Enrollment
60
Registered
2019-05-01
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

None listed

Interventions

Intervention1: Stroke Volume Variation or SVV Guided Fluid Therapy: Balanced salt solution boluses will be given over 15 min if stroke volume variation is more than 10 to 12 percent and will not be g

Sponsors

Sanjay Gandhi Postgraduate Institute of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients willing to participate patients with age more than 18 years and less than 70 years Selected as donor as per SGPGIMS donor criteria

Exclusion criteria

Exclusion criteria: Patients refusal to participate Patients with severe persistent peripheral vasoconstriction or arterial spasm such as in shock states Patients having coronary artery disease Patients of dilated cardiomyopathy with left ventricular ejection fraction less than 40 percent Patients with artificial hearts and ventricular assist devices Patients less than 18 years of age and more than 70 years of age Patients with severe persistent arrhythmias

Design outcomes

Primary

MeasureTime frame
To study and compare the intraoperative fluid requirement in selected groupsTimepoint: To study and compare the intraoperative fluid requirement in selected groups—

Secondary

MeasureTime frame
To compare the pain scores with Visual Analogue Scale in selected groupsTimepoint: 8 hourly from end of surgery till discharge;To study and compare the median length of stay in selected groupsTimepoint: duration calculated admission till the patients discharged;To Study the Perioperative events such as Nausea and Vomiting and any other complications in selected groupTimepoint: after end of surgery—

Countries

India

Contacts

Public ContactDr Pratyush Kar

Sanjay Gandhi Postgraduate Institute of Medical Sciences

drsandeepsahu@yahoo.co.in8004904598

Outcome results

None listed

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