COATI: Outpatient Left Laparoscopic Colectomy

Sponsor
Groupe Hospitalier de la Rochelle Ré Aunis (Other)
Overall Status
Recruiting
CT.gov ID
NCT04310839
Collaborator
Medtronic (Industry)
30
1
24.5
1.2

Study Details

Study Description

Brief Summary

The success of the enhanced recovery program after surgery leads us to consider outpatient management of the colectomy. To this end, the investigators have designed an observational and prospective study of left laparoscopic colectomy on an outpatient basis. The objective is to assess the harmlessness of this management compared to standard management in the context of a public hospital.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Colectomy

Detailed Description

In France, colectomy represents about 40,000 interventions per year, most of them scheduled, and 2/3 in a context of neoplasia. This surgery is associated with numerous postoperative complications. Since the start of Enhanced Recovery After Surgery (ERAS) in 1997, complications have been steadily reduced by optimizing surgical and anaesthetic techniques. At the same time, the average length of post-operative stay has decreased. In 2014, ERAS was the subject of recommendations by the French Society of Anaesthesia and Resuscitation, taken up by the French Health Authority (HAS) in 2016, and which are now an integral part of surgical management in colorectal surgery. More recently, two teams have set up an outpatient colectomy program. The three studies published on this subject show encouraging results, in a private structure, with no increase in postoperative complications.

In accordance with the recommendations on ERAS published by the HAS, a program involving pre-, per- and post-interventional investment, has been put in place. Patients are discharged on D0, followed by close monitoring by a home care nurse twice daily. This nurse is in charge of collecting clinical data in order to detect possible early signs of post-operative complications that would justify re-hospitalisation after a medical-surgical decision.

Study Design

Study Type:
Observational
Anticipated Enrollment :
30 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Outpatient Management of Patients With a Left Laparoscopic Colectomy
Actual Study Start Date :
Sep 15, 2020
Anticipated Primary Completion Date :
Sep 1, 2022
Anticipated Study Completion Date :
Oct 1, 2022

Arms and Interventions

Arm Intervention/Treatment
outpatient left laparoscopic colectomy

Left laparoscopic laparoscopic colectomy patient managed on an outpatient basis

Procedure: Colectomy
colectomy due to neoplastic (stage 1) or diverticulosis

Outcome Measures

Primary Outcome Measures

  1. 30-day readmission rate [30 days after surgery]

    Number of re-hospitalisation after a medical-surgical decision due to post-operative complications

Secondary Outcome Measures

  1. Pain measurement: pain rating scale [7 days after surgery]

    Score at the numerical pain rating scale

  2. Mobilization [Day 0]

    Time (in hours) between extubation and first mobilization

  3. Ileus [up to 7 days after surgery]

    Number of day between surgery and first gas / stool

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • American Society of Anesthesiologists Classification (ASA) score I and II,

  • Patient with an indication for scheduled left colectomy due to neoplastic (stage 1) or diverticulitis,

  • Patient residing less than 30 minutes from La Rochelle hospital,

  • Presence of a companion from the anaesthesia consultation onwards,

  • Presence of an attendant at the patient's discharge,

  • Perfect understanding of outpatient care, pathology and surgical procedure of the patient and accompanying person,

  • Informed of the study.

Exclusion Criteria:
  • ASA score 3 et 4,

  • Indication for a straight or transverse colectomy,

  • Neoplasia evolution > stage 1,

  • Presence of anticoagulant treatment,

  • Intraoperative bleeding > 500ml,

  • Conversion to laparotomy,

  • Severe anesthetic complication (Anaphylaxis, Difficult Intubation),

  • Persons deprived of their liberty by a judicial or administrative decision,

  • Persons of full age who are subject to a legal protection measure,

  • Persons unable to consent,

  • Persons who are not members of or beneficiaries of a social security scheme,

  • Patient's refusal to participate in the study.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Groupe Hospitalier de la Rochelle Ré Aunis La Rochelle France

Sponsors and Collaborators

  • Groupe Hospitalier de la Rochelle Ré Aunis
  • Medtronic

Investigators

  • Study Director: Alexandre Smirnoff, MD, Groupe Hospitalier de la Rochelle Ré Aunis

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Groupe Hospitalier de la Rochelle Ré Aunis
ClinicalTrials.gov Identifier:
NCT04310839
Other Study ID Numbers:
  • 2018/P01/280
First Posted:
Mar 17, 2020
Last Update Posted:
Jan 24, 2022
Last Verified:
Jan 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 24, 2022