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Enhanced Recovery After Surgery Promotes the Rehabilitation of Patients With Acute Gastrointestinal Perforation in Perioperative Period

H

Hebei Medical University

Status

Completed

Conditions

Acute Gastrointestinal Perforation
Enhanced Recovery After Surgery

Treatments

Behavioral: Traditional treatment methods.
Behavioral: The enhanced recovery after surgery

Study type

Interventional

Funder types

Other

Identifiers

NCT07008313
HebMU 20180065

Details and patient eligibility

About

The enhanced recovery after surgery(ERAS) has been gradually extended from its initial colorectal surgery to almost all surgical fields. However, there are few reports about the application value of ERAS in emergency surgery. The goal of this clinical trial is to evaluate the value of ERAS in the perioperative period of acute gastrointestinal perforation. All the patients will be treated by emergency operation. The changes of CRP, PA, PCT in Plasma 1 hour before operation and 1,3,7 days after operation, the operation time, the amount of bleeding during operation, the recovery time of intestinal function and the time of the first meal after operation,the incidence of postoperative complications, the degree of postoperative pain, the time of first out-of-bed activity, fatigue and mental status, quality of life, the length and the cost of hospital stay will be monitored and recorded.

Enrollment

362 patients

Sex

All

Ages

14 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age≥14years old and ≤80 years old
  • The initial diagnosis is acute gastrointestinal perforation

Exclusion criteria

  • Patients with unconsciousness,or patients with past psychiatric history
  • Patients with shock and/or severe organ failure
  • Patients who are pregnant
  • Patients with severe spinal deformity who are unable to receive epidural anesthesia

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

362 participants in 2 patient groups, including a placebo group

the enhanced recovery after surgery (ERAS) group
Experimental group
Description:
Patients were rehabilitated using the ERAS concept.
Treatment:
Behavioral: The enhanced recovery after surgery
the conventional surgical treatment (CST) group
Placebo Comparator group
Description:
Traditional treatment methods.
Treatment:
Behavioral: Traditional treatment methods.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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