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OpenTrials
Completed

NCT Number: NCT02852447

The Effect of Surgery for Non Endometriosic Ovarian Cysts on Ovarian Reserve

The main objective is to evaluate the ovarian reserve after laparoscopic cystectomy.

The secondary objective is the analysis of predictors of change in the ovarian reserve after surgery

Completed

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients with non endometriosis ovarian cysts
  • Age between 15-40 years
  • Regulars menses
  • Signed informed consent

Exclusion criteria

  • Patients with Previous surgery,
  • Patients with infertility,
  • Patients with endometriosis or
  • Patients with suspicious of malignance

Treatment and study plan

Primary outcomes

  1. differences in the ovarian reserve before and after surgery by Antimullerian Hormone

    Time frame: 3 months

  2. differences in the ovarian reserve before and after surgery by Antral Follicle Count

    Time frame: 3 months

Secondary outcomes

  1. Ovarian Size (mm)

    Time frame: 3 months

  2. Time of surgery (minutes)

    Time frame: 3 months

  3. Age (years)

    Time frame: 3 months

  4. BMI in kg/m2

    Time frame: 3 months

Sponsors and collaborators

Lead sponsor

Corporacion Parc Tauli

Other

Registry information

Official study title

The Effect of Surgery for Non Endometriosic Ovarian Cysts on Ovarian Reserve : A Prospective Study

Important dates

Study start
2014
Primary completion
2016
Study completion
2016
First posted
Aug 2, 2016
Registry last updated
Feb 23, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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