CClinicalTrials.gg
Sign In
RecruitingNCT06724380Updated Feb 12, 2025

Detection of Health Risk Situations in the Anesthesia Consultation.

An observational study in Surgical Procedures, Operative, sponsored by Consorci Sanitari de l'Alt Penedès i Garraf. Recruiting at 1 site in Spain. Open to participants aged 18 Years to 50 Years. Per ClinicalTrials.gov, last updated 2025-02-12.

Sponsored by Consorci Sanitari de l'Alt Penedès i Garraf · Observational

From the registry’s dates

  • Primary completion was expected by Dec 2025, 10 months ago, but the record still lists the study as recruiting.
  • Started Feb 2025; still recruiting 1 year 8 months later.
Study type
Observational
Model
Other
Time perspective
Retrospective
Enrollment
218
Ages
18 Years to 50 Years
Sex
All
01

Study summary

This study aims to estimate the proportion of patients seen in the anesthesiology consultation for planned surgery in whom a previously unknown health risk situation is detected (e.g., obesity, anemia, etc.).

02

Conditions studied

  • Surgical Procedures, Operative
03

In context

Lead sponsor

Consorci Sanitari de l'Alt Penedès i Garraf is the lead sponsor of 36 studies on the registry; 19 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 50 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients evaluated in person at the preoperative anesthesia consultation for a scheduled surgery indication.

Inclusion criteria

  • Men and women aged 18 to 50 years.

    • Indication for elective surgery.
    • In-person preoperative evaluation in the scheduled Anesthesiology consultation.

Exclusion criteria

Exclusion Criteria:

  • Indication for non-deferrable urgent surgery.
  • Pregnant women.
  • Pre-surgical visit outside the anesthesia consultation.
  • Incomplete preoperative evaluation, as indicated in the final section (preoperative judgment) of the anesthesia visit report.
05

Study design

Observational model
Other
Time perspective
Retrospective
Enrollment
218 participants (estimated)
Patient registry
No

Interventions

  • Otherunknown health risk situation

    a unknown health risk situation detected at anestesiology consult

06

What researchers measure

Primary outcomes

  1. unknown health risk situation

    proportion of patients with a unknown health risk situation

    Time frame: 1 year

07

Study locations

1 of 1 sites recruiting
  • Consorci Sanitari Alt Penedés-Garraf
    Vilafranca del Penedés, Barcelona, Spain
    Recruiting
08

References and documents

Individual participant data

Plan to share: Yes — IPD (without personal identification data) could be shared by requirement from other researchers after the end of the study, and only for research purposes and previous approval of promotor center of the study (CSAPG). Anyway, Spanish and European Union legal policy about data protection will strictly be followed (IPD will not be transferred outside European Union).

Supporting information: Study protocol

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 12, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06724380
Lead sponsor
Consorci Sanitari de l'Alt Penedès i Garraf
Responsible party
Sponsor
First posted
Dec 9, 2024
Start date
Feb 4, 2025
Primary completion
Dec 2025 (estimated)
Completion
Dec 2025 (estimated)
Last update
Feb 12, 2025

Study contacts

Laura Mingüell, MD
Contact
lminguell@csapg.cat
0034938960025
Noemí Casaponsa
Contact
recerca@csapg.cat
0034938960025 ext. 43197

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Other studies from this sponsor

Consorci Sanitari de l'Alt Penedès i Garraf

Start the discussion