Ignite Creation Date:
2024-05-06 @ 9:03 AM
Last Modification Date:
2024-10-26 @ 12:08 PM
Study NCT ID:
NCT02881541
Status:
WITHDRAWN
Last Update Posted:
2018-08-13
First Post:
2016-08-24
Brief Title:
Study of the Benefit of a Nurse IDE Pre and Post-operative Framework in Proctology Outpatient Surgery
Sponsor:
Fondation Hôpital Saint-Joseph
Organization:
Fondation Hôpital Saint-Joseph
Study Overview
Official Title:
Study of the Benefit of a Nurse IDE Pre and Post-operative Framework in Proctology Outpatient Surgery
Status:
WITHDRAWN
Status Verified Date:
2018-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
The investigator abandoned the project
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
IDEPROCTO
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
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 patients 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
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 patients 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
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None