Actively Recruiting

Phase Not Applicable
Age: 18Years - 40Years
FEMALE
NCT06350227

Impact of Different Hemostasis Methods on Ovarian Function and Fertility During Laparoscopic Ovarian Cystectomy of Benign Ovarian Cyst

Led by West China Second University Hospital · Updated on 2024-05-10

165

Participants Needed

1

Research Sites

85 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this study is to compare the impact of different hemostasis methods during laparoscopic ovarian cystectomy on ovarian function and fertility in women with benign ovarian cysts.

CONDITIONS

Official Title

Impact of Different Hemostasis Methods on Ovarian Function and Fertility During Laparoscopic Ovarian Cystectomy of Benign Ovarian Cyst

Who Can Participate

Age: 18Years - 40Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Women diagnosed with benign ovarian cysts needing surgery
  • Women who voluntarily choose laparoscopic ovarian cystectomy and sign consent
  • Women ready to accept random assignment to one of three hemostatic methods
  • Women aged 18 to 40 years old
  • Ultrasound diagnosis of unilateral or bilateral benign ovarian cysts 4-8 cm in size
  • No previous ovarian surgery, chemotherapy, or pelvic radiation
  • No history of endocrine disorders or endocrine therapy within 6 months before surgery
Not Eligible

You will not qualify if you...

  • Polycystic ovary syndrome
  • Pregnancy or breastfeeding
  • Active pelvic inflammatory disease or genital/extragenital cancer
  • Two or more previous pelvic or abdominal surgeries
  • Premature ovarian failure or menopause (e.g., AMH <1 ng/ml)
  • Conversion to open surgery
  • Refusal to sign consent or inability to attend follow-up
  • Cysts not originating from ovaries or with malignant features

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

West China Second University Hospital, Sichuan University

Chengdu, Sichuan, China

Actively Recruiting

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Research Team

Y

Yanru Long

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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