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Not yet recruitingNCT06667284Updated Nov 4, 2024

Gastroduodenal Intussusception: Two Cases of Gastroduodenal Intussusception Following Gastric Plication, Each Managed with a Different Approach.

An interventional study of Roux en y procedure and Omega brown procedure in Bariatric Surgery and Intussusception, sponsored by Ibn Al Nafees Hospital. Not yet recruiting. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-11-04.

Sponsored by Ibn Al Nafees Hospital · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Dec 2024, 1 year 10 months ago, but the record still lists the study as not yet recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
2
Allocation
Randomized
Ages
18 Years and older
Sex
All
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Study summary

The investigators received two female patients in the hospital who developed gastroduodenal intussusception following gastric plication procedure, requiring surgical treatment. Both patients presented with non-specific, atypical abdominal pain several months after the gastric plication. Both patients required surgical intervention, which included manual reduction of the plication followed by subtotal gastrectomy en bloc with Roux-en-Y reconstruction. In the second case, an Omega Brown anastomosis was performed, and a jejunostomy was created after the anastomosis in both patients.

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Conditions studied

  • Bariatric Surgery
  • Intussusception

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Keywords

  • case report
  • gastric plication
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In context

Intussusception

31 studies on the registry are indexed under Intussusception; 6 are open to participants now.

This study's planned enrollment of 2 is below the median of 78 across 16 interventional studies indexed under Intussusception.

Browse Intussusception studies →

Lead sponsor

This is the only study on the registry with Ibn Al Nafees Hospital as lead sponsor.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patients with gastro-duodenal intussusception following a gastric plication procedure.

Exclusion criteria

Exclusion Criteria:

  • children
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
2 participants (estimated)

Study arms

  • Active comparator
    Group a

    Roux en y procedure

    Procedure: Roux en y procedure

  • Active comparator
    Group b

    Omega Brown anastomosis

    Procedure: Omega brown procedure

Interventions

  • ProcedureRoux en y procedure

    subtotal gastrectomy en bloc with Roux-en-Y reconstruction, using TA 90 and GIA staplers. The length of the biliopancreatic limb was 50 cm, while the alimentary limb was 80 cm

  • ProcedureOmega brown procedure

    Gastrojejunal anastomosis with jejunojejunal anastomosis

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What researchers measure

Primary outcomes

  1. Comparison of management strategies for gastro-duodenal intussusception following gastric plication.

    The investigators compare the outcomes of managing bowel obstruction and abdominal pain after each surgery. The Investigator use small bowel obstruction prediction score index

    Time frame: 12 weeks following end of treatment.

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Study locations

No study locations are listed for this record.

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References and documents

Publications

  • Coco D, Leanza S, Fiume I. Small bowel obstruction: a prognostic score index for surgery - a review. Prz Gastroenterol. 2022;17(3):177-182. doi: 10.5114/pg.2022.118454. Epub 2022 Aug 3. PubMed 36127935 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 4, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06667284
Lead sponsor
Ibn Al Nafees Hospital
Collaborators
Damascus University
Responsible party
Yamen Madi (General surgeon, Damascus University) — Principal investigator
First posted
Oct 31, 2024
Start date
Oct 31, 2024 (estimated)
Primary completion
Dec 31, 2024 (estimated)
Completion
Jan 15, 2025 (estimated)
Last update
Nov 4, 2024

Study contacts

Yamen Madi, MD
Contact
yamen747@gmail.com
4915731165547

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Oct 2024. You cannot join it, but the record below documents what was studied.

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