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Clinical Trials/KCT0002854
KCT0002854Recruiting未知

Investigation of uterine (cervical, endometrial) carcinogenesis by identifying multiple interaction of human uterine (cervical, endometrial) microbiome using Meta-Omics analysis [Host – HPV – Microbiome – Environment]

CC Hospital0 sites1,800 target enrollmentStarted: TBDLast updated:

Trial Snapshot

Phase
未知
Status
Recruiting
Sponsor
Enrollment
1,800

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Observational Study

Eligibility Criteria

Ages
18(Year) to 65(Year) (—)
Sex
Female

Inclusion Criteria

  • 1) 18 years of age or older
  • 2) human papilloma virus(HPV)-negative women
  • 3) had normal for final diagnosis
  • 1) 18 years of age or older with sexually active
  • 2) human papilloma virus(HPV)-positive women
  • 3) had normal or cervical intraepithelial neoplasia(CIN), cervical cancer
  • 3. Endometrium
  • 1) 18 years of age or older
  • 2) women undergoing hysterectomy or curettage by any standard surgical approach
  • 3) undergoing hysterectomy for benign disease, hyperplasia, or any stage of endometrial cancer

Exclusion Criteria

  • 1) under 18 years
  • 2) had normal for final diagnosis, but human papilloma virus(HPV)-positive women
  • 3) no written informed consent
  • 1) under 18 years
  • 2) women who were pregnant or nursing
  • 3) had history of hysterectomy or treatment for cervical intraepithelial neoplasia(CIN) or cervical cancer during the 18 months previous to enrollment
  • 4) no written informed consent
  • 3. Endometrium
  • 1) under 18 years
  • 2) women who were pregnant or nursing
  • 3) had taken antibiotics within two weeks preceding surgery
  • 4) surgeon using morcellation during the hysterectomy procedure, due to the size of the uterus or for any other reason
  • 5) no written informed consent

Investigators

Sponsor
CC Hospital

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