Ignite Creation Date:
2024-10-26 @ 3:42 PM
Last Modification Date:
2024-10-26 @ 3:42 PM
Study NCT ID:
NCT06626802
Status:
COMPLETED
Last Update Posted:
None
First Post:
2024-09-24
Brief Title:
Steroid Versus Mitomycin-C Use in Pediatric Benign Recurrent Esophageal Stricture
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Intralesional Steroid Injection Versus Topical Mitomycin-C Use in Pediatric Benign Recurrent Esophageal Stricture A Randomized Control Trial
Status:
COMPLETED
Status Verified Date:
2024-10
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
To compare the efficacy of steroid injection versus topical mitomycin-C in the treatment of pediatric benign recurrent esophageal strictures The rationale for this study is to compare the two therapeutic options in order to measure their effectiveness in terms of improvement of Dysphagia Severity Score DSS
Detailed Description:
After taking approval from the Institutional Review Board of the university and taking the informed consent from parents patients fulfilling the inclusion and exclusion criteria will be enrolled in the study They will be then randomly allocated into two groups group A and group B Patients in Group A will be treated with esophageal dilation with a CRE balloon controlled radial expansion balloon After adequate dilation of stricture injection Mitomycin will be applied to the narrowest portion of the stricture Patients in Group B will be treated with esophageal dilation with a CRE balloon in the same manner After adequate dilation of stricture Triamcinolone injection will be injected into the narrowest portion of the stricture using a sclerotherapy injector Dysphagia Severity Score will be noted at start of intervention at 2 weeks after intervention and at 6 weeks post- intervention
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None