NCT05676164View on ClinicalTrials.gov

A Study to Evaluate the Safety and Efficacy of Oral Contrast Agent for Sonography

NACompletedINTERVENTIONAL

Enrollment

280

Participants

Timeline

Start Date

March 31, 2021

Primary Completion Date

August 22, 2022

Study Completion Date

August 22, 2022

Conditions

Unspecified Disorder of Stomach and Duodenum

Interventions

DEVICE

KANG XIAN

This product is a liquid composed of silica, stabilizer, xylitol, flavoring agent and water. The pH value of the product is 5.0 \~ 8.0, and the total heavy metal content (measured by Pb2+) is less than 10µg/ml.

DEVICE

TIAN XIA

The products are dark yellow granules made from rice, soybean, lotus root powder, orange peel, coix seed and yam.

Trial Locations (1)

Unknown

Qilu Hospital Of Shangdong University, Jinan

All Listed Sponsors

lead

Shandong Branden Med.Device Co.,Ltd

INDUSTRY

NCT05676164 - A Study to Evaluate the Safety and Efficacy of Oral Contrast Agent for Sonography | Biotech Hunter | Biotech Hunter