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Registry of Anesthesia and Perioperative Medicine (RAMP)

C

Clinica Alemana de Santiago

Status

Not yet enrolling

Conditions

Perioperative Complication
Anesthesia; Adverse Effect
Anesthesia Morbidity
Perioperative/Postoperative Complications
Anesthesia; Reaction
Anesthesia Complication

Treatments

Procedure: Anesthesia Intervention

Study type

Observational

Funder types

Other

Identifiers

NCT05869578
UIEC1166

Details and patient eligibility

About

To assess mortality and morbidity associated to anesthesia interventions

Full description

Currently evidence-based medicine is one of the most important tools guiding our medical practice. Part of this evidence has been generated from clinical records, which has allowed access to large databases from which relevant information has been obtained for perioperative risk stratification, searching for complications, having specific information on procedures, among others.

A clear example, especially useful daily in anesthesia work, is the NSQIP score, a tool that allows calculating perioperative risk according to the conditions of the patient and the surgery. NSQIP score is considered to make decisions in both the American and the European guidelines for preoperative evaluation for surgery.

Latin-American or Chilean databases are not available at the present time. Chile lacks of population perioperative databases, methodology and practice of medicine outcomes records, thus making necessary the generation of a retrospective/prospective registry.

The investigators expect that this registry will allow the collection of perioperative information appropriate to characterize the Chilean population, observe its evolution, and detect risk factors. Moreover, this registry will grant the investigators the means to design new research studies that may allow them to gather medical evidence of superior quality, thus benefiting patients with the best and safest interventions and procedures.

Enrollment

10,000 estimated patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • All individuals
  • Individuals agreeing to participate in the study by signing a consent

Exclusion criteria

  • The subjects who had insufficient data in their files

Trial contacts and locations

1

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Central trial contact

Patricio A Leyton, MD; Javiera A Vargas, MD

Data sourced from clinicaltrials.gov

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