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Feasibility and Therapeutic Potential of Free Fat Grafts in the Treatment of Esophageal Strictures (ESOGRAFT) (ESOGRAFT)

Primary Purpose

Esophageal Stricture, Fat Graft

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Stricture dilation with CRE balloon
Autologous fat grafting
Sponsored by
Hannes Kortekangas
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Esophageal Stricture focused on measuring Esophageal Stricture, Fat Graft, Dilation

Eligibility Criteria

18 Years - 99 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Esophageal stricture that has re-occurred at least once

Exclusion Criteria:

  • Malignant etiology of esophageal stricture

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    Esophageal stricture patients

    Arm Description

    Patients suffering from benign esophageal stricture are treated with through-the scope CRE dilation balloon. Free fat graft is gathered from the abdominal subcutaneous fat. Fat graft is prepared and injected to the stricture site.

    Outcomes

    Primary Outcome Measures

    Incidence of Treatment-Emergent Adverse Events at 3 months
    Types, severity and probability of procedure related adverse events
    Incidence of Treatment-Emergent Adverse Events at 12 months
    Types, severity and probability of procedure related adverse events

    Secondary Outcome Measures

    Change from Baseline Eckardt score at 3 months
    Eckardt score is a validated symptom questionnaire used to measure achalasia symptoms. Esophageal stricture symptoms are similar to achalasia symptoms. Sub scales: Dysphagia, retrosternal pain, regurgitation, weight loss. Each sub scale 0-3 points. 0=none, 1=occasional / less than 5 kg, 2=daily / 5-10kg, 3= each meal /more than 10 kg. Total 0-12 points.
    Change from Baseline Eckardt-score at 12 months
    Eckardt score is a validated symptom questionnaire used to measure achalasia symptoms. Esophageal stricture symptoms are similar to achalasia symptoms. Sub scales: Dysphagia, retrosternal pain, regurgitation, weight loss. Each sub scale 0-3 points. 0=none, 1=occasional / less than 5 kg, 2=daily / 5-10kg, 3= each meal /more than 10 kg. Total 0-12 points.
    Change from Baseline Stricture Lumen diameter at 3 months
    Stricture photographed and lumen diameter measurement. Unit: closed biopsy forceps diameter.
    Change from Baseline Stricture Lumen diameter at 12 months
    Stricture photographed and lumen diameter measurement. Unit: closed biopsy forceps diameter.
    Change from Baseline Stricture length at 3 months
    Stricture length measured using shaft of biopsy forceps. Unit: mm.
    Change from Baseline Stricture length at 12 months
    Stricture length measured using shaft of biopsy forceps. Unit: mm.

    Full Information

    First Posted
    January 6, 2020
    Last Updated
    February 28, 2021
    Sponsor
    Hannes Kortekangas
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04221867
    Brief Title
    Feasibility and Therapeutic Potential of Free Fat Grafts in the Treatment of Esophageal Strictures (ESOGRAFT)
    Acronym
    ESOGRAFT
    Official Title
    Feasibility and Therapeutic Potential of Free Fat Grafts in the Treatment of Esophageal Strictures
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    February 2021
    Overall Recruitment Status
    Unknown status
    Study Start Date
    August 15, 2021 (Anticipated)
    Primary Completion Date
    March 1, 2022 (Anticipated)
    Study Completion Date
    March 1, 2023 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor-Investigator
    Name of the Sponsor
    Hannes Kortekangas

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    In this study the investigators investigate the feasibility and therapeutic potential of free autologous fat grafting combined to dilation therapy in the treatment of benign esophageal strictures.
    Detailed Description
    In this study the investigators wish to proof the concept of free fat graft transfer into esophageal stricture via flexible video gastroscope.The investigators will recruit twenty patients suffering from (endoscopy proven) benign stricture of the esophagus. The Eckardt score is recorded upon recruitment and one day before operation. The operation is performed at the gastroenterology outpatient clinic in Turku University Hospital by a gastrointestinal surgeon. The patient is sedated with alfentanil and midazolam. First, abdominal liposuction (roughly 20 ml) is performed under local infiltration anesthesia. The fat graft is processed into nano-fat using Tulip GEMS Single-Use NanoTransfer Set. Esophagoscopy with gastroscope is performed and stricture is visually graded (location, length, lumen) and photographed. Then esophageal stricture is biopsied with biopsy forceps and dilated with through-the-scope CRE(controlled radial expansion) balloon dilator. Prepared fat graft is injected beneath the mucosal layer at the stricture site (volume of 0,1-0,5 ml) at three locations. Patients are either discharged after two hours follow up or admitted to the inpatient ward, depending on the pre- and postoperative condition. Patients are contacted by phone 1 week after the operation. Post-operative symptoms are recorded and patients are requested to contact the researcher if needed. Patient records are screened for pre- and postoperative symptoms, medication, long term illnesses and possible postoperative contacts to hospital. Follow-up esophagoscopy is performed and biopsies taken three and 12 months after the first operation. The stricture site is visually graded and photographed. The Eckardt score is recorded. If the patient has problems with eating (Eckardt score dysphagia points more than 1) the stricture is re-dilated and fat grafting repeated. If a patient would have recurrence in dysphagia before three months the patient is treated according to normal routine and dilation is repeated earlier. The follow-up time is 12 months counting from the last fat grafting.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Esophageal Stricture, Fat Graft
    Keywords
    Esophageal Stricture, Fat Graft, Dilation

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    20 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Esophageal stricture patients
    Arm Type
    Experimental
    Arm Description
    Patients suffering from benign esophageal stricture are treated with through-the scope CRE dilation balloon. Free fat graft is gathered from the abdominal subcutaneous fat. Fat graft is prepared and injected to the stricture site.
    Intervention Type
    Procedure
    Intervention Name(s)
    Stricture dilation with CRE balloon
    Intervention Description
    Esophageal stricture is treated by dilation therapy.
    Intervention Type
    Procedure
    Intervention Name(s)
    Autologous fat grafting
    Intervention Description
    Autologous fat graft is gathered and injected to stricture
    Primary Outcome Measure Information:
    Title
    Incidence of Treatment-Emergent Adverse Events at 3 months
    Description
    Types, severity and probability of procedure related adverse events
    Time Frame
    3 months
    Title
    Incidence of Treatment-Emergent Adverse Events at 12 months
    Description
    Types, severity and probability of procedure related adverse events
    Time Frame
    12 months
    Secondary Outcome Measure Information:
    Title
    Change from Baseline Eckardt score at 3 months
    Description
    Eckardt score is a validated symptom questionnaire used to measure achalasia symptoms. Esophageal stricture symptoms are similar to achalasia symptoms. Sub scales: Dysphagia, retrosternal pain, regurgitation, weight loss. Each sub scale 0-3 points. 0=none, 1=occasional / less than 5 kg, 2=daily / 5-10kg, 3= each meal /more than 10 kg. Total 0-12 points.
    Time Frame
    3 months
    Title
    Change from Baseline Eckardt-score at 12 months
    Description
    Eckardt score is a validated symptom questionnaire used to measure achalasia symptoms. Esophageal stricture symptoms are similar to achalasia symptoms. Sub scales: Dysphagia, retrosternal pain, regurgitation, weight loss. Each sub scale 0-3 points. 0=none, 1=occasional / less than 5 kg, 2=daily / 5-10kg, 3= each meal /more than 10 kg. Total 0-12 points.
    Time Frame
    12 months
    Title
    Change from Baseline Stricture Lumen diameter at 3 months
    Description
    Stricture photographed and lumen diameter measurement. Unit: closed biopsy forceps diameter.
    Time Frame
    3 months
    Title
    Change from Baseline Stricture Lumen diameter at 12 months
    Description
    Stricture photographed and lumen diameter measurement. Unit: closed biopsy forceps diameter.
    Time Frame
    12 months
    Title
    Change from Baseline Stricture length at 3 months
    Description
    Stricture length measured using shaft of biopsy forceps. Unit: mm.
    Time Frame
    3 months
    Title
    Change from Baseline Stricture length at 12 months
    Description
    Stricture length measured using shaft of biopsy forceps. Unit: mm.
    Time Frame
    12 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    99 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Esophageal stricture that has re-occurred at least once Exclusion Criteria: Malignant etiology of esophageal stricture
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Hannes A Kortekangas, Surgeon
    Phone
    +35823139192
    Email
    hannes.kortekangas@tyks.fi
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Pauliina Hartiala, Surgeon
    Organizational Affiliation
    Turku University Hospital
    Official's Role
    Study Director

    12. IPD Sharing Statement

    Learn more about this trial

    Feasibility and Therapeutic Potential of Free Fat Grafts in the Treatment of Esophageal Strictures (ESOGRAFT)

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