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Reversal of Roux-en-Y Gastric Bypass: A Swedish National Cohort Study

Reversal of Roux-en-Y Gastric Bypass: A Swedish National Cohort Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07347093
Enrollment
199
Registered
2026-01-16
Start date
2025-11-01
Completion date
2026-05-31
Last updated
2026-01-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Complications After Bariatric Surgery, Gastric Bypass Surgery, Revisional Bariatric Surgery

Keywords

Roux-en-Y gastric bypass, Anatomical reversal, Indications, Complications, Outcomes

Brief summary

Objective: To investigates incidence, indications, symptom relief, complications, and weight outcomes after Roux-en-Y gastric bypass (RYGB) reversal. Background: RYGB is an effective treatment for obesity, but in rare cases may be associated with severe long-term complications requiring RYGB reversal. Evidence on incidence and outcomes is limited. Methods: This nationwide, multi-center, retrospective cohort study included all patients undergoing RYGB reversal in Sweden between 2007 and 2023. Data were obtained from the Scandinavian Obesity Surgery Registry (SOReg) and medical records.

Interventions

None listed

Sponsors

Vrinnevi Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adult patients (≥ 18years) who underwent reversal of RYGB between 2007 and 2023.

Exclusion criteria

* Emergency reversal due to bowel ischemia * Reversal following other bariatric procedures (e.g. gastric banding) * Partial/functional reversals (e.g., gastro-gastric fistula or anastomosis between the Roux-limb and gastric remnant, without full reversal of RYGB)

Design outcomes

Primary

MeasureTime frameDescription
Symptom reliefThrough study completion, an average of 2 years.Symptom relief is classified as no, partial, or complete improvement. Complete improvement was defined as full resolution of the index symptom (e.g., cessation of hypoglycemia, pain-free status without analgesics). Partial improvement denoted a clinically meaningful reduction in symptom severity or frequency that did not meet criteria for complete resolution. No improvement indicated persistent symptoms.

Secondary

MeasureTime frameDescription
Indications for surgeryThrough study completion, an average of 2 years.Indications are categorized as abdominal pain, malnutrition, gastrointestinal symptoms, post-bariatric hypoglycemia, and psychological distress, and reported as number (frequencies).
Weight outcome after surgeryThrough study completion, an average of 2 years.Weigth \[in kilograms\] will be reported at baseline (before surgery), at one year follow-up, and two-year follow-up.
ComplicationsAt 30-day follow-up and one-year follow-up after surgery.Complications after surgery are registered as any complication and major complication (defined as Clavien-Dindo classification \>=3b), presented as number (frequencies).
HeightThrough study completion, an average of 2 yearsHeight (in meters) will be used to report BMI (in kg/m2).
BMIThrough study completion, an average of 2 years.Weight (in kilograms) and height (in meters) will be combined to report BMI (in kg/m2) at baseline (before surgery), at one year follow-up, andat two-year follow-up.

Countries

Sweden

Contacts

PRINCIPAL_INVESTIGATOREllen A Andersson, MD

Department of Surgery, Vrinnevi Hospital, Norrköping, and Department of Biomedical and Clinical Sciences, Linköping University, Linköping, Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026