Actively Recruiting

Age: 18Years +
All Genders
ID06146270

National Register of Postoperative Outcomes in the Russian Federation A Multicenter Observational Study

Led by Russian Federation of Anesthesiologists and Reanimatologists · Updated on 2025-04-04

162000

Participants Needed

16

Research Sites

4 weeks

Total Duration

On this page

Sponsors

R

Russian Federation of Anesthesiologists and Reanimatologists

Lead Sponsor

K

Kuban State Medical University

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are conducting a national multicenter observational study to develop a Russian national calculator for predicting the risk of postoperative complications and mortality. The study focuses on adult patients undergoing elective and emergency surgeries in various surgical fields including obstetrics, gynecology, urology, orthopedics, and more. The aim is to identify risk factors that lead to unfavorable postoperative outcomes and to create a comprehensive database for better understanding and prediction of surgical risks. The study includes two cohorts: Cohort A will assess the incidence of primary outcomes such as 30-day mortality and complications, and Cohort B will identify risk factors and develop a risk calculator validated across different surgical specialties. Data collection involves filling out basic and additional checklists quarterly across centers to capture detailed surgical and postoperative information. The study period spans from 2024 to 2028 with monitoring of outcomes up to one year after surgery. Participants will be followed for various outcomes including 30-day and 90-day mortality and complications, length of stay in intensive care and hospital, multiple organ failure, ICU syndrome, readmission rates, and one-year mortality. Researchers will analyze long-term results and the influence of factors such as anesthesia type, urgency of surgery, age, comorbidities, and oncological conditions. The study is organized by the Russian Federation of Anesthesiologists and Reanimatologists and aims to improve postoperative care through validated risk assessment tools integrated into a national calculator.

CONDITIONS

Brief Title

Russian Registry of Surgical OutcomeS

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patients aged 18 years and older undergoing elective surgery in specified surgical fields
  • Adult patients aged 18 years and older undergoing emergency surgery in specified or other surgical areas
  • Surgery areas include obstetrics, gynecology, breast, urology and kidneys, endocrine surgery, maxillofacial surgery, orthopedics and traumatology, lower and upper abdominal cavity, liver and biliary tract, thoracic surgery, vascular surgery, neurosurgery, cardiac surgery, and other specified areas
Not Eligible

You will not qualify if you...

  • Lack of informed consent from the patient
  • Complications caused by anesthesiologist manipulations
  • Surgical interventions without an anesthesiologist-resuscitator
  • Incomplete or incorrectly filled checklists
  • Deviations from the study protocol

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surgery and Immediate Post-operative Care

Duration - Up to 30 days after surgery

Participants undergo elective or emergency surgery, followed by immediate post-operative care to monitor initial recovery and complications.

Visits as part of routine surgical and post-operative care

Post-operative Follow-up

Duration - Up to 90 days after surgery

Participants are observed for postoperative complications, recovery progress, and mortality at 90 days following surgery.

Follow-up visits up to 90 days post-surgery

Long-term Monitoring

Duration - Up to 1 year after surgery

Participants are monitored for readmission and mortality outcomes up to one year after surgery to assess long-term postoperative results.

Periodic follow-up visits up to 1 year post-surgery

Trial Site Locations

Total: 16 locations

1

The First City Clinical Hospital. n.a. E. E. Volosevich

Arkhangelsk, Russia

Actively Recruiting

2

Kuzbass Clinical Emergency Hospital named after M.A. Podgorbunsky

Kemerovo, Russia

Actively Recruiting

3

Regional clinical hospital №2

Krasnodar, Russia, 350012

Actively Recruiting

4

Kuban State Medical University

Krasnodar, Russia, 350063

Actively Recruiting

5

Krasnodar regional hospital №2 (Kuban State Medical University)

Krasnodar, Russia

Not Yet Recruiting

6

Regional clinical hospital

Krasnoyarsk, Russia

Actively Recruiting

7

Federal research and clinical center of intensive care medicine and rehabilitology

Moscow, Russia

Actively Recruiting

8

Loginov Moscow Clinical Scientific Center

Moscow, Russia

Not Yet Recruiting

9

Military Medical Academy

Moscow, Russia

Not Yet Recruiting

10

Moscow cancer research Institute named after P. A. Herzen

Moscow, Russia

Actively Recruiting

11

Moscow Regional Research and Clinical Institute, Moscow, Russia

Moscow, Russia

Not Yet Recruiting

12

Moscow regional research clinical Institute named after M. F. Vladimirsky

Moscow, Russia

Actively Recruiting

13

Orenburg City N.I. Pirogov Clinical Hospital

Orenburg, Russia

Actively Recruiting

14

North-Western State Medical University named after Ilya I. Mechnikov,

Saint Petersburg, Russia

Not Yet Recruiting

15

Regional clinical hospital №2

Vladivostok, Russia

Actively Recruiting

16

Clinical city hospital № 40

Yekaterinburg, Russia

Actively Recruiting

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Research Team

I

Igor Zabolotskikh, MD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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