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Banded gastric bypass in super morbid obesity

Banded Roux-en-Y gastric bypass in patients with super morbid obesity (BRandY-study): protocol of a cohort study with 5-year follow-up

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON21611
Enrollment
142
Registered
2019-10-15
Start date
2019-10-15
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Super morbid obesity

Interventions

Laparoscopic banded Roux-en-Y gastric bypass (B-RYGB) Laparoscopic non-banded Roux-en-Y gastric bypass (NB-RYGB)

Sponsors

Bariatric-Solutions GmbH Kaltenbacherstrasse 24 CH 8260 Stein am Rhein Phone: +41 52 741 65 00 Fax: +41 52 741 65 02
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: • Age 18-65 years • Preoperative BMI 50 kg/m2 or greater • Banded Roux-en-Y gastric bypass or non-banded Roux-en-Y gastric bypass performed • Informed consent and committed to follow-up appointments

Exclusion criteria

Exclusion criteria: • Prior bariatric procedures

Design outcomes

Primary

MeasureTime frame
Weight loss and non-response (insufficient weight loss and weight regain) within 5 years after surgery—

Secondary

MeasureTime frame
obesity related comorbidities and medications, (band-related) morbidity and mortality, complications and re-operations, patient satisfaction and health-related quality of life—

Contacts

Public ContactMarleen Romeijn

Máxima Medisch Centrum

Marleen.Romeijn@mmc.nl+3140-8886286

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)