Influence of Postoperative Rehabilitation and Pre- and Postoperative Physical Activity in Abdominal Surgery

Abdominal Injuries Clinical Trial

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT02829125
• Other study ID #: 6254
• Status: Recruiting
• Phase: N/A
• First received: June 17, 2016
• Last updated: May 10, 2017
• Start date: January 1, 2015
• Est. completion date: January 2018

Study information

• Verified date: January 2015
• Source: University Hospital, Strasbourg, France
• Contact: Jean-Philippe STEINMETZ, MD
• Phone: 33 (0)3 88 12 72 56
• Email: Jean-Philippe.STEINMETZ[@]chru-strasbourg.fr
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The concept of early rehabilitation (ERAS: enhanced after-surgery recovery) was introduced by Kehlet et al. in 1995, as part of the colon surgery. This program is a support for patients combining laparoscopic surgery, epidural analgesia, early refeeding and rapid mobilization of patients. This strategy targets multiple elements (20 items) to support pre-, intra- and postoperative patients. This reduces the pain and the different organ dysfunction induced by surgical stress significantly decreasing length of hospital stay, postoperative morbidity and costs.

Furthermore, early mobilization of patients is fundamental to the ERAS method. Few studies have analyzed the influence of preoperative exercise on postoperative rehabilitation.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 400
• Est. completion date: January 2018
• Est. primary completion date: January 1, 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion criteria

1. non-cancerous and cancerous pathology

2. signed Consent

3. Every patient operated on a scheduled or emergency abdominal surgery

Exclusion criteria

1. inability to give informed about information

2. minor Patient

Related Conditions & MeSH terms

• Abdominal Injuries

Locations

Country	Name	City	State
France	Service de Chirurgie Digestive - Hôpital de Hautepierre	Strasbourg

Sponsors (1)

Lead Sponsor	Collaborator
University Hospital, Strasbourg, France

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	quality of life questionnaire		before and after the operation