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Sleeve Gastrectomy as a Standard Bariatric Procedure

Establishing Laparoscopic Sleeve Gastrectomy as a Standard Procedure at a Swedish Bariatric Center

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05336331
Enrollment
1015
Registered
2022-04-20
Start date
2021-01-01
Completion date
2025-12-31
Last updated
2022-04-20

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

Conditions

Postoperative Complications

Keywords

bariatric surgery, laparoscopic Roux-en-Y gastric bypass, laparoscopic sleeve gastrectomy, Morbid obesity, Weight loss, Metabolic control, Metabolic syndrome, Complication risk

Brief summary

This study compared differences in weight loss, comorbidity resolution and complications and reoperations between a recently established sleeve gastrectomy (SG) and prior laparoscopic Rox-en-Y gastric bypass (RYGB).

Detailed description

This retrospective study with prospectively collected registry data presents results from establishment of SG as standard procedure for morbid obesity. Our first 368 patients operated with a SG were compared to 647 patients previously operated with a (RYGB. Perioperative data and results up to 2 years postoperatively regarding weight control, metabolic control as well as complications/reoperations necessary were registered. In summary, a RYGB was associated with a longer operation time and higher rates of late complications and reoperations. Diabetes resolution was similar in both groups but patients with a RYGB had greater weight loss and significant improvement in hypertension and dyslipidemias.

Interventions

PROCEDURESG or a RYGB

operation type differed between a partial gastrectomy (SG)or a combined restrictive/malabsorptive

Sponsors

Umeå University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Patients with either a BMI 35 or higher with comorbidity, or patients with a BMI of 40 or more without known comorbidity associated, undergoing a primary laparoscopic bariatric surgery in Sundsvall,Sweden 2010-01-01 to 2018-06-10.

Exclusion criteria

* All other patients undergoing a bariatric surgery during this time frame

Design outcomes

Primary

MeasureTime frameDescription
Weight lossafter 6 weeksweight and height will be combined to report various measurements of BMI in kg/m\^2
Changes in Diabetesafter 1 yearmeasured as fasting plasma glucose and/or Hemoglobin A1c
Changes in Hypertensionafter 1 yearmeasured as Systolic- and Diastolic Blood Pressure
Changes in hypertriglyceridemia (plasma-level >1.7 mmol/l)after 1 yearmeasured as hypertriglyceridaemia (plasma-level \>1.7 mmol/l)
Changes in Hypercholesterolemia (LDL-C > 3.0 mmol/L and/or HDL-C < 1.0 mmol/L).after 1 yearsMeasured as Hypercholesterolemia (Plasma concentration of LDL \>3.0 mmol/L and/or of HDL \< 1.0 mmol/L).
Duration of surgeryFrom the start of the operation until completion, in average 62 minutesOperation time in minutes
Duration of hospital stayFrom time of operation until discharge, in average 1.7 daysDuration of hospital stay in days
Early complicationsAt six weeksComplications occurred until six weeks from operation
Early reoperationsAt six weeksReoperations occurred until six weeks from operation
Late complicationsFrom six weeks until 2 years from operationComplications occurred from six weeks until 2 years from operation
Late reoperationsFrom six weeks until 2 years from operationReoperations occurred from six weeks until 2 years from operation

Countries

Sweden

Outcome results

None listed

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