Skip to content

Feasibility of Ambulatory Hysterectomy

Preliminary Study About the Feasibility of Ambulatory Hysterectomy: Bicentric Study in Caen UH and Amiens UH

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03290339
Acronym
AMETHYST
Enrollment
30
Registered
2017-09-21
Start date
2017-09-06
Completion date
2019-12-06
Last updated
2017-10-11

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

Conditions

Surgery; Maternal, Uterus or Pelvic Organs, Affecting Fetus

Keywords

one-day surgery, hysterectomy, ambulatory

Brief summary

Hysterectomy is one of the most performed surgery in women. Public authorities wish that one-day surgery become a majority and hysterectomy could be part of it in the future. The aim of this study is to determine the feasibility of ambulatory hysterectomy. Patients and methods: Investigators will realize an observational descriptive survey based on questionnaires in two surgical gynecology units. Women under 70 years old, who undergo hysterectomy will be included.

Interventions

PROCEDUREhysterectomy

laparoscopic hysterectomy and vaginal hysterectomy

Sponsors

Amiens University Hospital
CollaboratorOTHER
University Hospital, Caen
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* women, undergo surgery for hysterectomy by laparoscopy or vaginal procedure

Exclusion criteria

* comorbidities included: heart disease, anti-coagulant treatment, anti-aggregant treatment; sleep apnea syndrome, laparotomy laparoconversion if hysterectomy associated with appendectomy and/or, omentectomy and/or, lymph nodes dissection

Design outcomes

Primary

MeasureTime frame
PADSS scoreDay 0 post surgery

Secondary

MeasureTime frameDescription
patient satisfactionDay 1questionnaire

Countries

France

Contacts

Primary ContactFabien CHAILLOT
chaillot-f@chu-caen.fr+33 2 31 06 57 74

Outcome results

None listed

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