Surgical Procedures, OperativeNCT06724380
Detection of Health Risk Situations in the Anesthesia Consultation.
An observational study of Surgical Procedures, Operative, run by Consorci Sanitari de l'Alt Penedès i Garraf at 1 site in Spain.
Trial 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.). Read more about this study
- Who is it for?
- Ages 18 to 50 years
- Conditions the study is for
- Surgical Procedures, Operative
- What is being tested?
- unknown health risk situation
- How many people
- 218 participants
- Where
- 1 siteSpain
- Study dates
- 4 Feb 2025to Dec 2027
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 50 years
- All sexes
- No healthy volunteers
- Adult
Study population: Patients evaluated in person at the preoperative anesthesia consultation for a scheduled surgery indication.
Who may be able to join
- Men and women aged 18 to 50 years.
- Indication for elective surgery.
- In-person preoperative evaluation in the scheduled Anesthesiology consultation.
Who cannot join
- 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.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Spain1 site, 1 recruiting
- Recruiting
Consorci Sanitari Alt Penedés-Garraf
Vilafranca Del Penedés, Barcelona
Laura Mingüell, MD, 0034938960025, lminguell@csapg.cat
Noemí Casaponsa, 0034938960025 ext. 43197, recerca@csapg.cat
About this study
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.).
- Conditions
- Surgical Procedures, Operative
- Being tested
- unknown health risk situation
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
unknown health risk situationOther
a unknown health risk situation detected at anestesiology consult
What is being measured
The primary outcome is the main question the study is designed to answer.
unknown health risk situation
proportion of patients with a unknown health risk situation
Measured: 1 year
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted9 Dec 2024
- Study start4 Feb 2025
- Primary completionDec 2027 (estimated)
- Study completionDec 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Surgical Procedures, OperativeStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Other
- Time perspective
- Retrospective
- Enrolment
- 218 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Consorci Sanitari de l'Alt Penedès i Garraf
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06724380
- Sponsor's protocol ID
- CSAPG-64
- Status last verified
- Oct 2026
- First submitted
- 5 Dec 2024
- Last updated
- 28 Oct 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- 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).
Study at a glance
From the registry record, last updated by the sponsor on 28 Oct 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Detection of Health Risk Situations in the Anesthesia Consultation.
- ClinicalTrials.gov ID
- NCT06724380
- Acronym / sponsor ID
- CSAPG-64
- Conditions
- Surgical Procedures, Operative
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 218 participants (estimated)
- Lead sponsor
- Consorci Sanitari de l'Alt Penedès i GarrafUniversity, hospital or other
- Study start
- 4 Feb 2025 (actual)
- Primary completion
- Dec 2027 (estimated)
- Study completion
- Dec 2027 (estimated)
- First posted
- 9 Dec 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.).
Study design
- Observational model
- Other
- Time perspective
- Retrospective
Who may qualify
- Ages
- 18 to 50 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult
- Study population
- Patients evaluated in person at the preoperative anesthesia consultation for a scheduled surgery indication.
Key inclusion criteria (3 listed)
- Men and women aged 18 to 50 years.
Key exclusion criteria (4 listed)
- 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.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| unknown health risk situationa unknown health risk situation detected at anestesiology consult | Other | – |
Primary outcome
unknown health risk situation
Time frame: 1 year
proportion of patients with a unknown health risk situation
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 28 Oct 2026.
- Individual participant dataSharing planned: 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).
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Surgical Procedures, Operative, run by Consorci Sanitari de l'Alt Penedès i Garraf at 1 site in Spain.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 28 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Spain. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Laura Mingüell, MD (0034938960025, lminguell@csapg.cat), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
unknown health risk situation (time frame: 1 year). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 Oct 2026.