临床试验/PER-047-18

PER-047-18招募中未知

STUDY OF THE STAINING SOLUTION MEDIATED BY THE FOLATO RECEIVER (FRD BY ITS ACRONYMS IN ENGLISH) IN THE DETECTION OF CERVICAL CANCER.

GY HIGHLAND BIOTECH LLC,0 个研究点目标入组 638 人开始时间: 2019年4月3日最近更新: 2023年12月18日

适应症

试验速览

阶段: 未知
状态: 招募中
发起方: GY HIGHLAND BIOTECH LLC,
入组人数: 638

研究概览入排标准研究者记录与标识符相似试验

研究概览

简要总结

暂无简介。

研究设计

研究类型: Interventional

入排标准

入选标准

•-MUJER BETWEEN 20-60
•-DIAGNOSIS: WOMAN WHO NEEDS TO BE PERFORMED GYNECOLOGICAL PELVIC EXAMINATION FOR CERVICAL CANCER DISCARD. WOMEN WHO HAVE REGULAR CONDITIONS TO PERFORM A COLPOSCOPY. (DO NOT HAVE VAGINAL SHOWS, NO SEXUAL RELATIONS AND NOT BEING MENTRUANDO)

排除标准

•MUJERES WITH TOTAL HYSTERECTOMY. WOMEN WHO HAD CERVICAL SURGERY, INCLUDING CONIZATION, PROCEDURE OF ELECTRO SURGICAL EXCISION (LEEP, OF ITS ABBREVIATIONS IN ENGLISH) AND INFRARED RAYS. WOMEN WITH SERIOUS CERVICAL HEMORRHAGE OF CONTACT-PREGNANT WOMEN - WOMEN WITH ACUTE INFLAMMATION OF THE UTERINE NECK AND / OR THE VAGINA - WOMEN WHO WERE ALREADY DIAGNOSED WITH CONNIC2 + WOMEN WHO USE INJECTABLE OR ORAL DRUGS AGAINST CANCER

研究者

发起方

GY HIGHLAND BIOTECH LLC,

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