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