Study Phase III Comparison of Superiority, Open With Blind Appraiser, to Evaluate the Efficacy and Safety of Barium Sulphate 66.7% With V (OPTI-BAR) Compared to Proceedings in Inert Radiological Examinations for the Diagnosis of Diseases for Image the Tratogastrointstinal

Alko do Brasil

Status: Unknown

Conditions: X-ray Examinations of the Gastrointestinal Tract

Study type: Observational

Funder types: Industry

Identifiers

NCT01629719

ALK 002-001

Details and patient eligibility

About

Phase III clinical study, two samples, with assessor blind for the purpose of evaluating the efficacy and safety of the superiority of the use of barium sulphate 66.7% w/v (Opti-bar) as a contrast X-ray (X-ray).

Enrollment: 73 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Men and women over 18 who need x-rays gastrointestinal tract with contrast;
• Healthy patient, ambulatory;
• Willingness to comply with the requirements of the study after signing an informed consent and (hit).

Exclusion criteria

• Pregnant or lactating women;
• Patients allergic to barium sulfate, latex rubber or simethicone;
• Patients who have asthma, eczema, cystic fibrosis, heart disease, high blood pressure, rectal cancer, colostomy, obstruction in the stomach or intestines, pseudotumor cerebri, blocking stomach or intestinal disease, Hirsch or pseudotumor cerebri;
• Patients who have recently undergone a rectal biopsy or surgery or a recent history of drilling into your esophagus, stomach or intestines; Patients who have already participated in another clinical protocol in the last six months;
• Other clinical criteria that in the opinion of the study investigator could compromise the welfare of the patient or interfere with the results expected from the study.