Viewing Study NCT04008667


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Study NCT ID: NCT04008667
Status: UNKNOWN
Last Update Posted: 2019-07-05
First Post: 2019-06-29
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: The Effect of Acupoint Application on Postoperative Ileus
Sponsor: li xiong
Organization:

Study Overview

Official Title: The Effect of Acupoint Application on Postoperative Ileus: a Randomized Controlled Trial
Status: UNKNOWN
Status Verified Date: 2019-07
Last Known Status: NOT_YET_RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This study aims to verify the therapeutical effect and mechanism of acupoint application on postoperative ileus.
Detailed Description: Postoperative ileus (POI) is a common disorder of gastrointestinal motility characterized by abdominal distension, nausea, vomiting and delayed passage of flatus or stool, which develops after every abdominal surgical procedure. POI increases risk of developing postoperative complications, decreases the bed turnover rate and prolongs the average duration of hospitalization, increasing the expense of both patients and hospitals. Although the Pathophysiological mechanism of POI remains unclear, recent researches suggests the inflammatory responses after surgery might be responsible for the gastrointestinal motility disorder. Acupoint application is a traditional chinese intervention which has been used in treating gastrointestinal motility disorder resulted from other causes. In this study, we aims to verify the therapeutical effect and mechanism of acupoint application on postoperative ileus.

Study Oversight

Has Oversight DMC: True
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: