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Status unknownNCT03950011BDD RAACUpdated May 14, 2019

Database for Data Collection in the Context of an Enhanced Recovery After Surgery Program in Oncology Surgery

An observational study in Oncology, sponsored by Institut Paoli-Calmettes. Status unknown at 1 site in France. Open to female participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2019-05-14.

Sponsored by Institut Paoli-Calmettes · Observational

The sponsor has not verified this record recently (last verified May 2019), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
500
Ages
18 Years and older
Sex
Female
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Study summary

Enhanced Recovery After Surgery Programs (ERP) includes multimodal approaches of perioperative patient's clinical pathways designed to achieve early recovery after surgery and a decreased length of hospital stay (LOS).

Read the detailed description

This database would also allow an objective evaluation of the quality of the surgical management and the follow-up.

One of the evaluation criteria will be measured by the quantity and quality of publications from this database, and also by the increase in the activity of the service concerned.

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Conditions studied

  • Oncology

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Keywords

  • Enhanced Recovery After Surgery Program (ERP)
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In context

Neoplasms

9,365 studies on the registry are indexed under Neoplasms; 2,489 are open to participants now.

This study's planned enrollment of 500 is above the median of 204 across 1,683 observational studies indexed under Neoplasms.

Browse Neoplasms studies →

Lead sponsor

Institut Paoli-Calmettes is the lead sponsor of 168 studies on the registry; 50 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Any patient operated including hysterectomy and or curettage, posterior pelvectomy, conventional laparoscopic or assisted robot, or laparotomy at the Paoli-Calmettes Institute from 01 2016 to 12 2017, and incrementation from 2018.

Inclusion criteria

  • Any patient operated including hysterectomy and or curettage, posterior pelvectomy, conventional laparoscopic or assisted robot, or laparotomy at the Paoli-Calmettes Institute from 01 2016 to 12 2017, and incrementation from 2018.

Exclusion criteria

Exclusion Criteria:

  • Non applicable.
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Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
500 participants (estimated)
Target follow-up
1 Year
Patient registry
Yes

Groups and cohorts

  • ERP

    Any patient requiring oncologic surgery, including hysterectomy or curettage, posterior pelvectomy, conventional laparoscopic or assisted robotic surgery, or laparotomy for cervical or cervical cancer or ovarian cancer, body or cervix uterus and ovaries as well as benign pathologies or borderline malignancy.

    Procedure: Enhanced recovery after surgery program

Interventions

  • ProcedureEnhanced recovery after surgery program

    Enhanced Recovery After Surgery Programs (ERP) includes multimodal approaches of perioperative patient's clinical pathways designed to achieve early recovery after surgery and a decreased length of hospital stay (LOS).

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What researchers measure

Primary outcomes

  1. Data collection

    Restrospective and prospective data collection

    Time frame: 4 years

Secondary outcomes

  1. Evaluation of the quality of surgical management

    characteristics of the surgery according to the type of diagnosis

    Time frame: 4 days

  2. Post-operative complications

    post-operative complications in hospitalization and post-operative complications after leaving hospital

    Time frame: 4 days

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Study locations

1 of 1 sites recruiting
  • Institut Paoli Calmettes
    Marseille, Bouches Du Rhone 13009, France
    Recruiting
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References and documents

Publications

  • Lambaudie E, de Nonneville A, Brun C, Laplane C, N'Guyen Duong L, Boher JM, Jauffret C, Blache G, Knight S, Cini E, Houvenaeghel G, Blache JL. Enhanced recovery after surgery program in Gynaecologic Oncological surgery in a minimally invasive techniques expert center. BMC Surg. 2017 Dec 28;17(1):136. doi: 10.1186/s12893-017-0332-9. PubMed 29282059 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 14, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT03950011
Lead sponsor
Institut Paoli-Calmettes
Responsible party
Sponsor
First posted
May 14, 2019
Start date
Jan 1, 2016
Primary completion
Jan 1, 2020 (estimated)
Completion
Feb 28, 2020 (estimated)
Last update
May 14, 2019

Study contacts

Dominique Genre
Contact
drci.up@ipc.unicancer.fr
+33491223778

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in May 2019. You cannot join it, but the record below documents what was studied.

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