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Laparoscopic Splenectomy in Children (splenectomy)

Primary Purpose

Laparoscopic Splenectomy, Children, Benign Blood Diseases

Status
Completed
Phase
Phase 1
Locations
Study Type
Interventional
Intervention
laparoscopic splenectomy
Sponsored by
Tanta University
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional health services research trial for Laparoscopic Splenectomy focused on measuring laparoscopic splenectomy,, children, prognostic score, benign hematological diseases

Eligibility Criteria

3 Years - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • children with benign hematological diseases

Exclusion Criteria:

  • malignant hematological diseases

Sites / Locations

    Outcomes

    Primary Outcome Measures

    prognosis of procedure
    number of patients with peritoneal collections, number of patients having pancreatitis, number of patients staying more than two days postoperative

    Secondary Outcome Measures

    Full Information

    First Posted
    February 17, 2021
    Last Updated
    February 19, 2021
    Sponsor
    Tanta University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04763733
    Brief Title
    Laparoscopic Splenectomy in Children
    Acronym
    splenectomy
    Official Title
    Prognostic Scoring System of Laparoscopic Splenectomy in Children With Benign Hematological Diseases.
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    February 2021
    Overall Recruitment Status
    Completed
    Study Start Date
    January 2, 2012 (Actual)
    Primary Completion Date
    February 14, 2021 (Actual)
    Study Completion Date
    February 16, 2021 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Tanta University

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    Yes
    Device Product Not Approved or Cleared by U.S. FDA
    Yes
    Pediatric Postmarket Surveillance of a Device Product
    Yes

    5. Study Description

    Brief Summary
    Laparoscopic splenectomy (LS) gained popularity since it has been described for the first-time during nineties of past century. It has become "golden method" for splenectomy in all ages including children
    Detailed Description
    Background: laparoscopic splenectomy (LS) gained popularity during the last years in pediatric age group. Benign hematological diseases represent the main indications of that procedure. There are some score systems of difficulty of the technique but they are for adult patients. The aim is to develop a prognostic score system of LS in children with benign hematological diseases. Methods: LS was performed in all children with benign hematological diseases. LS was done by the same team. They operated children in lateral decubitus position. The control of pedicle was achieved using bipolar sealing devices, polymer clips or endoscopic linear staplers. Preoperative, operative, and postoperative data were recorded and analyzed. Children were divided into two groups A and B according to the development of complications.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Laparoscopic Splenectomy, Children, Benign Blood Diseases
    Keywords
    laparoscopic splenectomy,, children, prognostic score, benign hematological diseases

    7. Study Design

    Primary Purpose
    Health Services Research
    Study Phase
    Phase 1
    Interventional Study Model
    Single Group Assignment
    Masking
    Participant
    Allocation
    N/A
    Enrollment
    137 (Actual)

    8. Arms, Groups, and Interventions

    Intervention Type
    Other
    Intervention Name(s)
    laparoscopic splenectomy
    Intervention Description
    surgical
    Primary Outcome Measure Information:
    Title
    prognosis of procedure
    Description
    number of patients with peritoneal collections, number of patients having pancreatitis, number of patients staying more than two days postoperative
    Time Frame
    from day 0 to 7 days

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    3 Years
    Maximum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: children with benign hematological diseases Exclusion Criteria: malignant hematological diseases

    12. IPD Sharing Statement

    Plan to Share IPD
    No

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    Laparoscopic Splenectomy in Children

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