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Use of Blood Pressure increasing medicines in cancer surgery and their impact on patients after surgery

Evaluation of Intraoperative Vasopressor Usage, Its patterns, and Postoperative Outcomes in Major Abdominal Oncologic Surgery - a prospective cohort study. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/05/110043
Enrollment
100
Registered
2026-05-05
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Health Condition 1: C00-D49- Neoplasms

Interventions

Intervention1: Nil: Nil Intervention2: Nil: Nil

Sponsors

ACTREC, TMC
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Undergoing major oncologic surgery (Gastrointestinal, gynaecology, urology procedures) 2.ASA I-III Elective or emergency surgery 3.Intra-operative vasopressor infusion initiated 4.Planned postoperative ICU/HDU admission

Exclusion criteria

Exclusion criteria: 1.Vasopressor bolus use only (no infusion) 2.Day-care surgeries

Design outcomes

Primary

MeasureTime frame
To evaluate the relationship between intra-operative vasopressor use and postoperative adverse outcomes, including: 1.Acute kidney injury (KDIGO ) 2.Postoperative infection (CDC) 3.30-day mortality 4.Other clinically relevant complications (e.g., need for critical care escalation) (Clavien Dindo greater than and equal to grade III) Timepoint: upto 30 days

Secondary

MeasureTime frame
To describe the current patterns of vasopressor administration during the intra-operative period, including type of agent, total dose, timing, & duration.Timepoint: Intraoperative Period(days of surgery);To identify patient, surgical, & intra-operative factors associated with increased vasopressor requirement, such as type of surgery, baseline comorbidities, blood loss, or intra-operative instabilityTimepoint: From day of surgery to 30 days;To evaluate variation in vasopressor use between surgical specialties & determine whether differences persist after adjusting for patient & procedural characteristics.Timepoint: From day of surgery to 30 days;To describe patterns of fluid therapy (crystalloid & colloid administration) & explore their interaction with vasopressor use & postoperative outcomesTimepoint: From day of surgery to 30 days;. To explore the relationship between intra-operative adverse events (e.g., significant blood loss, arrhythmias, unexpected instability) & subsequent vasopressor dosing patterns.Timepoint: From day of surgery to 30 days

Countries

India

Contacts

Public ContactDr Mohit Hooda

Advanced Centre for Treatment, Research and Education in Cancer (ACTREC)

divyabhagwat30@gmail.com7208460727

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 11, 2026