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Effectiveness Accompaniment Perioperative Patients With Psychiatric Illness on the Lives Perioperative

Effectiveness Accompaniment Perioperative Patients With Psychiatric Illness on the Lives Perioperative

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02857322
Acronym
VEPSY
Enrollment
88
Registered
2016-08-05
Start date
2017-01-31
Completion date
2020-05-31
Last updated
2016-08-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Psychiatric Disorders

Brief summary

The experimental strategy is to develop a specific device about the anesthetic and surgical acts for a subject with a documented psychiatric condition and to benefit from surgery. This device is based on 3 stages: pre-operative phase, Phase perioperative and postoperative phase. A nurse anesthetist will come into contact with the subject the day before surgery. This contact will be concomitant with the pre-anesthesia visit. She explained about the general organization of the arrival in the operating room. The interview will be a minimum of 15 minutes and beyond if necessary. This will be accompanying this the next day in the operating room in order to optimize its hospitality and installing the block, guide the subject through all the steps before falling asleep. Finally, even accompanying will be present upon awakening the subject in the recovery room.

Interventions

OTHERAccompanying patient's specific perioperative

Sponsors

Assistance Publique Hopitaux De Marseille
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* adult subject; * Subject with chronic mental illness defined by ICD-10 classification \[ICD-10, 1992\], corresponding to psychoses say no emotional or affective psychoses say; * Subject to which mental pathology is evolving for more than 6 months; * Topic targeted for elective surgery; * Topic judged capable of performing a self-administered questionnaire;

Exclusion criteria

* minor, pregnant or nursing women, about not being affiliated to the social security scheme, subject under guardianship; * Subject with a mental illness do not belong to sections of ICD-10 contained in inclusion criteria; * Subject to benefit from surgery as part of the emergency;

Design outcomes

Primary

MeasureTime frameDescription
experiences of the perioperative periodsecond dayassessment using a self-administered questionnaire called EVAN. This is a standardized questionnaire and validated, whose purpose is to understand the experience of perioperative anesthesia multidimensional way. It contains 28 items describing 6 dimensions (anxiety, discomfort, fear, pain and discomfort, explanations, needs). dimensional scores range from 0 (worst experience) to 100 (best experience).

Countries

France

Contacts

Primary ContactMaryline Mascarin
drci@ap-hm.fr0491382747

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026