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

Sponsor
Corporacion Parc Tauli (Other)
Overall Status
Completed
CT.gov ID
NCT02852447
Collaborator
(none)
30
Enrollment
1
Location
25
Duration (Months)
1.2
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

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

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    30 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    The Effect of Surgery for Non Endometriosic Ovarian Cysts on Ovarian Reserve : A Prospective Study
    Study Start Date :
    Nov 1, 2014
    Actual Primary Completion Date :
    Oct 1, 2016
    Actual Study Completion Date :
    Dec 1, 2016

    Outcome Measures

    Primary Outcome Measures

    1. differences in the ovarian reserve before and after surgery by Antimullerian Hormone [3 months]

    2. differences in the ovarian reserve before and after surgery by Antral Follicle Count [3 months]

    Secondary Outcome Measures

    1. Ovarian Size (mm) [3 months]

    2. Time of surgery (minutes) [3 months]

    3. Age (years) [3 months]

    4. BMI in kg/m2 [3 months]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    15 Years to 40 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    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

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Corporació Sanitària Parc Tauli Sabadell Barcelona Spain 08208

    Sponsors and Collaborators

    • Corporacion Parc Tauli

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Laura Costa-Canals, MD, Corporacion Parc Tauli
    ClinicalTrials.gov Identifier:
    NCT02852447
    Other Study ID Numbers:
    • CPT-GINE-2016
    First Posted:
    Aug 2, 2016
    Last Update Posted:
    Feb 23, 2017
    Last Verified:
    Feb 1, 2017
    Additional relevant MeSH terms:
    Cysts
    Ovarian Cysts

    Study Results

    No Results Posted as of Feb 23, 2017