Fast-Track Colorectal Surgery in Senior Patients

NCT01646190 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 150

Last updated 2012-07-23

No results posted yet for this study

Summary

Fast-track (FT) surgery is a multimodal, multidisciplinary-team approach to reduce perioperative surgical stress and injury after colorectal surgery, resulting in lower morbidity and enhanced recovery. As fast-track approach could probably be the most beneficial for senior patients to reduce postoperative morbidity and better preserve independency, only scarce information is available in senior population. Therefore a randomized controlled trial is initiated in our institution compare a senior dedicated fast-track approach to modern standard care after colorectal surgery.

Conditions

  • Colorectal Disorders

Interventions

DIETARY_SUPPLEMENT

Preoperative Carbohydrate load

oral intake in the evening before surgery and 2-3h before intubation

PROCEDURE

individualized i.v fluids therapy

by Transoesophageal aortic US-Doppler done intraoperatively

BEHAVIORAL

Fasting state after midnight

No preoperative glucose load

BEHAVIORAL

No Nasogastric tube postoperatively

Withdrawal after complete awakening in operating room

BEHAVIORAL

urinary catheter removal

at POD 1

BEHAVIORAL

Oral liquids

0.3-0.5L oral liquids at 6h postoperatively on POD 0

BEHAVIORAL

Stimulation of inspirex utilization

using 6-8 times/day to prevent pulmonary atelectasis

BEHAVIORAL

Mobilization

First active mobilization 6h after surgery (2h on chair or 45° sitting in bed), \>4h out of bed on POD1, \>6h on POD2, complete at POD3

OTHER

Preanesthetic medication

Preanesthetic oral medication before surgery

Sponsors & Collaborators

  • University Hospital, Geneva

    lead OTHER

Principal Investigators

  • Sandrine Ostermann, MD, PhD · University Hospital, Geneva

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-12-31
Primary Completion
2013-12-31
Completion
2013-12-31

Countries

  • Switzerland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01646190 on ClinicalTrials.gov