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Enhanced Recovery After Hepatic Surgery (MultiPAS).

Enhanced Recovery After Hepatic Surgery Versus Conventional Care : a Controlled Randomized Monocentric Trial (MultiPAS).

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02715427
Acronym
MultiPAS
Enrollment
80
Registered
2016-03-22
Start date
2016-04-30
Completion date
Unknown
Last updated
2016-04-04

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

Conditions

Liver Surgery

Brief summary

Enhanced rehabilitation programs are based on new therapies and treatment combinations to reduce the length of hospitalization, duration of postoperative convalescence, morbidity, but also the overall cost of care. The operating stress and hypercatabolic conditions surrounding the surgery are sources of complications. In this enhanced rehabilitation approach, the principle is to fight through a series of actions against this surgical stress. Several North American studies, Chinese, Scandinavian or Batavian have shown the feasibility and the interest of enhanced perioperative rehabilitation in liver surgery. Nevertheless, there is not until now French data concerning the assessment of enhanced rehabilitation in liver surgery. The main objective of the study is to compare the effectiveness of the implementation of a multimodal management program after liver surgery in a French university center compared to conventional care. Secondary objectives of the study are to compare an enhanced rehabilitation program in liver surgery versus conventional treatment in terms of morbidity and mortality in the immediate postoperative period and until day 90, length of hospital stay, blood loss and the delay to bowel mobility recovery. Compliance to the program in both groups will also be evaluated.

Interventions

OTHERConventional care
OTHEREnhanced recovery

Sponsors

University Hospital, Angers
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Patient to be operated on for hepatectomy in Universitary Hospital of Angers * No emergency surgery * No bilio-digestive anastomosis * Body Mass Index between 18 and 40 kg/m2 * Preoperative morbidity status graded with the American Society of Anesthesiologists (ASA) between I to III * Affiliated to the national health insurance

Exclusion criteria

* Pregnant woman * Patient who doesn't speack french * Colorectal surgery combined * Postoperative stay predictable in critical care unit * Patient under law protection

Design outcomes

Primary

MeasureTime frameDescription
Day number to functional recovery90 daysThe evaluation of time to functional recovery is scored once a day. A patient is fully functionally recovered when all of the following criteria are satisfied: 1. adequate pain control with oral analgesia: Post-operative pain is rated by the numeric rating scale. Nurses ask patients the intensity of their current pain on a scale of 0 (no pain) to 10 (worst possible pain). To satisfy this criterion, patient must rate their pain between 0 to 3 with only oral analgesics. 2. restoration of mobility to an independent level We decided to use the Groningen Activity Restriction Scale for rated the difference between preoperative and postoperative mobility level. To satisfy this criterion, patient must have the same score in postoperative. 3. absence of intravenous fluid administration for at least 24 hours. 4. ability to eat solid foods well tolerated for at least 24 hours to satisfy this criterion. 5. normal or decreasing serum bilirubin level and international normalised ratio.

Countries

France

Contacts

Primary ContactEmilie Lermite, MD-PhD
EmLermite@chu-angers.fr02 41 35 36 18
Backup ContactJulien Barbieux, MD
02 41 35 36 18

Outcome results

None listed

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