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Study of the Benefit of a Nurse (IDE) Pre and Post-operative Framework in Proctology Outpatient Surgery

Study of the Benefit of a Nurse (IDE) Pre and Post-operative Framework in Proctology Outpatient Surgery

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02881541
Acronym
IDEPROCTO
Enrollment
0
Registered
2016-08-29
Start date
2015-05-04
Completion date
2015-05-04
Last updated
2018-08-13

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

Conditions

Proctology, Surgery

Brief summary

Evaluate the complement of patient care course in the development of proctology outpatient surgery (CAP) by providing: * An additional preoperative nurse consultation day hospital * And a phone call from a nurse at D + 1 of the operation This corresponds to a reinforced support.

Detailed description

Main objective of the study: help improve the care of patients in CAP including during their exit after surgery. To evaluate the quality of patient care related to this enhanced system is a lever of development assistance outpatient surgical activity. Secondary Objectives: To evaluate the impact of this new organization * Satisfaction of patients and caregivers * The effectiveness of the management of patients' pain Study period: 3 months extendable a month, no start date announced Workforce to include 100 patients at 3 months (10 per week), 50 in the enhanced support group and 50 in the group usual care Expected results: The main objective evaluation criteria: Evaluation support the success rate. Evaluation performed 45 days after the patient's surgery. Secondary objectives: patient satisfaction (telephone questionnaire to 45 days of operation), caregivers, pain assessment (painkillers booklet completed by the patient during his first consultation), consultation or rehospitalization for emergency patients and finally degree trust the doctor vis-à-vis this new support.

Interventions

PROCEDUREUsual care

Sponsors

Fondation Hôpital Saint-Joseph
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

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

Inclusion criteria

* Patient man or woman major * Patient primary surgery and requiring care in CAP * Patient affiliated to a social security scheme or of such a scheme

Exclusion criteria

* Bedridden patient and / or not communicating * Patient opposing his participation in the study after information * Patient has already undergone anal surgery

Design outcomes

Primary

MeasureTime frame
Assessment of the success rate of the treatment using intern questionary scoreDay 45 after surgery

Secondary

MeasureTime frame
Assessment of patient satisfaction by intern phone questionary ScoreDay 45 after surgery

Outcome results

None listed

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