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Clinical Trials in Spain / NCT07615855
Starting soon Observational

RIDECLAS: Delphi Classification of RICA Pathway Recommendations

NCT07615855 · tracked via the Priya Life Science Spain tracker
Phase
Observational
Started
2026-06-01
Last updated
2026-05-29

Condition(s) studied

Enhanced Recovery After SurgeryPerioperative CareSurgical Care

Investigational drug(s) / intervention(s)

Modified Delphi questionnaire

Modified Delphi questionnaire: Sequential online questionnaires used to rate and classify proposed RICA Pathway recommendations. This is not a clinical intervention and does not involve patient care, drugs, devices, or invasive procedures.

Study summary

RIDECLAS is an observational, prospective, non-interventional consensus study using a modified Delphi methodology. The study aims to obtain expert consensus on the classification and final formulation of recommendations for the RICA Pathway, an enhanced recovery pathway for adult surgery. Participants will be healthcare professionals with experience in enhanced recovery, perioperative medicine, surgery, anesthesiology, nursing, rehabilitation, or related disciplines. Experts will complete sequential online questionnaires. Individual responses will remain confidential, and aggregated anonymized feedback will be provided between Delphi rounds. The study does not involve patients, clinical interventions, biological samples, drugs, or medical devices.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * Healthcare professional or researcher with relevant clinical or scientific experience in enhanced recovery pathways, perioperative medicine, surgery, anesthesiology, nursing, rehabilitation, or related disciplines. At least 5 years of professional experience. Membership in GERM or participation in professional networks related to enhanced recovery in adult surgery. Willingness to participate in the planned Delphi rounds. Provision of electronic informed consent. Exclusion Criteria: * Failure to meet the predefined professional experience criteria. Failure to provide informed consent. Failure to complete the first Delphi round. Duplicate or incomplete responses that cannot be validated for analysis.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Department of Surgery Zaragoza Zaragoza

More Universidad de Zaragoza trials in Spain

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07615855 on ClinicalTrials.gov ↗ ← All trials in Spain