VATS IN PATIENTS WITH ADVANCED OVARIAN MALIGNANCIES

Sponsor
Alexandria University (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT05840029
Collaborator
(none)
68
1
22.9
3

Study Details

Study Description

Brief Summary

Ovarian cancer is the seventh most common cancer and the fifth leading cause of death in women worldwide.

About 70% of patients with epithelial ovarian cancer present with advanced disease which will require a combination of cytoreductive surgery and chemotherapy to give them their best chance of long term survival.The presence of macroscopic pleural disease-especially if undetected and unresected after primary debulking surgery-may alter treatment decision-making and markedly affect survival. Video-Assisted Thoracoscopic Surgery (VATS) allows surgeons, through a minimally invasive approach, to not only drain the pleural effusion but also evaluate macroscopic pleural disease and, when possible, resect gross tumor.

Few studies reported that VATS altered the therapeutic management in ovarian cancer patients leading to an upstaging or down-staging when compared to the CT staging. Therefore, this study will prospectively assess the role of VATS in the diagnosis and management of supradiaphragmatic disease as well as evaluate the impact of VATS findings on the decision of surgical management in patients with advanced ovarian cancer FIGO (The International Federation of Gynecology and Obstetrics) stage III/IV.

Condition or Disease Intervention/Treatment Phase
  • Procedure: VIDEO-ASSISTED THORACOSCOPIC SURGERY

Study Design

Study Type:
Observational
Actual Enrollment :
68 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
THE ROLE OF VIDEO-ASSISTED THORACOSCOPIC SURGERY IN PATIENTS WITH ADVANCED OVARIAN MALIGNANCIES
Actual Study Start Date :
Jun 1, 2021
Actual Primary Completion Date :
Jan 30, 2023
Anticipated Study Completion Date :
Apr 30, 2023

Arms and Interventions

Arm Intervention/Treatment
Group A: Patients who will get neoadjuvant chemotherapy based on VATS finding.

Patients will be considered to receive neoadjuvant chemotherapy if there is residual intrathoracic disease

Procedure: VIDEO-ASSISTED THORACOSCOPIC SURGERY
A minimally invasive approach, to not only drain the pleural effusion but also evaluate macroscopic pleural disease and, when possible, resect gross tumor.
Other Names:
  • VATS
  • Group B: Patients who will proceed into debulking surgery based on VATS finding.

    Patients will be considered to be eligible for complete debulking, if VATS showed no intrathoracic tumor or if VATS achieves complete removal of tumor nodules through intraoperative frozen section histopathological examination.

    Procedure: VIDEO-ASSISTED THORACOSCOPIC SURGERY
    A minimally invasive approach, to not only drain the pleural effusion but also evaluate macroscopic pleural disease and, when possible, resect gross tumor.
    Other Names:
  • VATS
  • Outcome Measures

    Primary Outcome Measures

    1. Prediction of intrathoracic disease using chest-CT results compared to the standard reference results using VATs [3 weekS]

      Comparison between the Chest-CT results in preoperative evaluation of supra-diaphragmatic disease will be compared to the intra-operative VATS evaluation results to evaluate the role of the VATS in those patients

    Secondary Outcome Measures

    1. The rate of change in the treatment plan according to VATs results [1 week]

      The number of patients that will receive different treatment plan after detection of intrathoracic disease using VATs

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    20 Years to 80 Years
    Sexes Eligible for Study:
    Female
    Inclusion Criteria:
    • FIGO stage III/IV ovarian cancer with or without pleural effusion
    Exclusion Criteria:
    1. Previously treated ovarian disease.

    2. Patient unfit for single lung ventilation.

    3. Patients with previous lung surgery.

    4. Patients with possible intrapleural adhesions.

    5. Patients who had pulmonary resection.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Alexandria University Alexandria Egypt 21131

    Sponsors and Collaborators

    • Alexandria University

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Alexandria University
    ClinicalTrials.gov Identifier:
    NCT05840029
    Other Study ID Numbers:
    • VATS and ovarian cancer
    First Posted:
    May 3, 2023
    Last Update Posted:
    May 3, 2023
    Last Verified:
    Nov 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Alexandria University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of May 3, 2023