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Recruiting Not applicable

Same Day Ambulatory Appendectomy (SAMBA)

NCT05691348 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2023-07-17
Last updated
2026-03-31

Condition(s) studied

Appendicitis

Investigational drug(s) / intervention(s)

Ambulatory appendectomyConventional appendectomy

Ambulatory appendectomy: Appendectomy will be performed in outpatient surgery unit. Patient will be discharge from the hospital the same day as surgery

Conventional appendectomy: Appendectomy will be performed in digestive surgery department. Patient will be discharge from the hospital the day after surgery: he will spend a night under observation

Study summary

The potential benefit of outpatient care for this common digestive emergency is considerable, both for the patients themselves and for the public health system:

1. Optimization of the care pathway, reducing the length of stay in hospital (a major issue in the context of the COVID-19 (coronavirus disease) pandemic) liberating patient beds and staff, and reducing the risk of nosocomial exposure.
2. Improved patient satisfaction compared to waiting for hours in the emergency department due to lack of hospital beds.
3. Non-inferiority of care in an outpatient unit in terms of quality and safety in day hospitalization.
4. Significant decrease in the overall cost of this pathology as a result of a reduction in the hospital stay.

Eligibility

Sex
ALL
Min age
15 Years
Max age
74 Years
Healthy volunteers
No
Inclusion Criteria: * Patients aged 15-74 years * BMI ≤ 35 kg/m2 * Uncomplicated acute appendicitis confirmed by imaging (ultrasound and/or CT and/or MRI) * Temperature ≤ 38,1°C and \> 35,5°C * Appendix diameter \> 6mm and ≤ 15mm * Without effusion or with only localized peri-appendicular effusion * Infiltration of peri-appendicular fat without abscess or plastron * No sign of perforation * Leukocytes ≤ 18,000G/L AND * CRP (C reactive protein) ≤ 60mg/L * If pain, calmed by level 3 analgesic at maximum * Ambulatory criteria * Availability of monitoring by a relative during the 12 hours after discharge from the hospital * Residence located less than 20 minutes by car from a health center (hospital or clinic) * Access to a telephone mobile or fixed in case of problems * Signature of the written informed consent form by the patient * If the patient is a minor, signature of the written informed consent form by both parents or their legal representative * Affiliation to a French health insurance scheme or equivalent Exclusion Criteria: * Criteria that exclude ambulatory care such as an ASA score (Physical status score) \> 2, severe or uncontrolled comorbidities, severe pulmonary disease including obstructive sleep apnea, anticoagulation or antiplatelet drug or contraindication to ambulatory surgery such as intubation difficulties * Presence of active cancer, a malignant hemopathy, drug addiction, coagulopathy, immunosuppressive treatment * Non-acute or interval appendectomy, i.e. after antibiotic treatment of a complicated appendicitis of the plastron or drainage of an appendicular abscess; * History of pelvic surgery * Vulnerable people: pregnant or breast-feeding women (patients will undergo a pregnancy test: plasmatic β-hCG (human chorionic gonadotropin) or urinary test), adult under guardianship or deprived of freedom. Pregnant women are considered to have a full stomach, with risk of inhalation at anesthetic induction and represent a contraindication to ambulatory surgery. In addition, the need to perform abdominal surgery on a pregnant woman requires obstetric monitoring that is difficult to reconcile with management in an outpatient surgery unit (need for obstetric ultrasound or monitoring). * Suspicion of a tumor of the appendix : Mucocele and pseudomyxoma, Carcinoid tumor, Adenocarcinoma of the appendix, Another type of tumor

Primary outcome measure(s)

  • To demonstrate that outpatient care, compared with conventional care, in selected patients with acute uncomplicated appendicitis operated by laparoscopy, is non-inferior in terms of overall morbi-mortality on the 30th postoperative day. — 30 days post surgery
    Morbi-mortality will be assessed by classifying post-operative complications according to Clavien-Dindo classification. It will be compared between both groups ("ambulatory pathway" versus "conventional hospitalization" CONV) on the 30th postoperative day. The Clavien-Dindo classification was originally published in 2004 in the Annals of Surgery for elective general surgery. Later, it has been objectively validated for all surgical specialties. This classification ranks complications from 0 (no complication) to 5 (death). Complications that potentially lead to long-lasting disability after discharge (e.g.: paralysis of a vocal cord after thyroid surgery) are highlighted in the present classification by a suffix ("d" for disability). This suffix indicates that a long-term follow-up is required to comprehensively evaluate the outcome and related long-term quality of life.

Trial sites (33)

FacilityCityRegionStatus
Hôpitaux Pédiatriques de Nice CHU - Lenval Nice Alpes Maritimes Not Yet Recruiting
CHU de Nice Nice Alpes-Maritimes Recruiting
CHU de Bordeaux Bordeaux Aquitaine Not Yet Recruiting
CH de Troyes Troyes Aube Not Yet Recruiting
CHU Grenoble Alpes La Tronche Auvergne-Rhône-Alpes Recruiting
Hôpital Edouard HERRIOT Lyon Auvergne-Rhône-Alpes Recruiting
CHU de Saint-Etienne - Hôpital Nord Saint-Priest-en-Jarez Auvergne-Rhône-Alpes Recruiting
CH de Voiron Voiron Auvergne-Rhône-Alpes Recruiting
APHM Hôpital Nord Marseille Bouches-du-Rhône Recruiting
CHU Minjo Besançon Bourgogne-Franche-Comté Not Yet Recruiting
CHU de Rennes Rennes Brittany Region Not Yet Recruiting
Hôpital Robert Debré - CHU de Reims Reims Grand Est Recruiting
Hôpital Beaujon (APHP) Clichy Hauts de Seine Not Yet Recruiting
CHU Amiens-Picardie Amiens Hauts-de-France Recruiting
Clinique de Saint-Omer Blendecques Hauts-de-France Not Yet Recruiting
HIA Percy Clamart Hauts-de-Seine Not Yet Recruiting
CHU de Tours Tours Indre Et Loire Not Yet Recruiting
CHU de Reims Reims Marne Not Yet Recruiting
CH de Dax Dax New Aquitaine Recruiting
CH de Mont de Marsan Mont-de-Marsan New Aquitaine Recruiting
Hôpital Cochin APHP Paris Paris Not Yet Recruiting
CHU d'Angers Angers Pays de la Loire Region Recruiting
Hôpital d'Instruction des armées Laveran Marseille Provence-Alpes-Côte d'Azur Region Recruiting
Hôpital d'Instruction des armées Sainte Anne - BCRM Toulon Toulon Provence-Alpes-Côte d'Azur Region Recruiting
Clinique du Val d'Ouest Écully Rhones-Alpes Not Yet Recruiting
Hôpital Avicenne Bobigny Île-de-France Region Recruiting
Hôpital Louis-Mourier Colombes Île-de-France Region Not Yet Recruiting
APHP Pitié Salpetrière Paris Île-de-France Region Not Yet Recruiting
APHP Lariboisière Paris Île-de-France Region Recruiting
Hia Begin Saint-Mandé Île-de-France Region Not Yet Recruiting
Clinique de l'Estrée Stains Île-de-France Region Not Yet Recruiting
CHU de La Réunion Saint-Denis La Réunion Recruiting
CHU de La Réunion Saint-Pierre La Réunion Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05691348 on ClinicalTrials.gov ↗ ← All trials in France