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Safety of endoscopic intragastric balloon

Safety study of endoscopic intragastric balloon for obese patients with endocrine metabolism disease

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs042190108
Enrollment
10
Registered
2020-01-20
Start date
2020-02-12
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Obesity with metabolic disease Obesity, Metabolic disease

Interventions

None

Sponsors

Yamashita Taro
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) BMI 27.5 kg / m2 or more 2) Metabolic disorders (Diabetes, hypertension, dyslipidemia, obesity according to the diagnostic criteria of the Japan Diabetes Society, The Japanese Society of Internal Medicine, Japan Arteriosclerosis Disease Prevention Guidelines) 3) Insufficient weight control in medical treatment including diet for more than 6 months 4) Age 20 to 80 5) Performance status (PS) is 0 or 1 by ECOG criteria 6) The latest inspection value within 7 days before registration (may be the same day one week before registration date) satisfies all the following. 1 white blood cell count less than 10,000 / mm3 2 number of neutrophils more than 1,500 / mm3 3 Hemoglobin more than 9.0 g / dL (no blood transfusion within 7 days prior to blood collection for the test used for registration) 4 platelet count more than 10 x 10 4 / mm 3 5 Total bilirubin less than 1.5 mg / dL 6 creatinine less than 2 mg / dL

Exclusion criteria

Exclusion criteria: 1) History of surgery on the stomach 2) Infections that require systemic treatment (except for viral hepatitis) 3) Women who are pregnant or have pregnancy possibility 4) Difficult to participate because it has a mental disease or symptoms that interfere with daily life. 5) Serious complications (heart failure, renal failure, liver failure, intestinal paralysis, intestinal obstruction etc.) 6) In addition, research principal investigator or the research division physician judged inappropriate 7)Participants who have been given sufficient explanations, and with sufficient understanding and consent from the patients themselves for their participation in this study

Design outcomes

Primary

MeasureTime frame
Safety of endoscopic intragastric balloon

Secondary

MeasureTime frame
1. Changes in body composition (fat circumference, fat mass, lean mass, bone mass measured by impedance method or DXA method) 2. Transition of metabolic disease related markers 3. Changes in stool bacteria and virus flora

Contacts

Public ContactTomoyuki Hayashi

Kanazawa University Hospital

tohayashi@m-kanazawa.jp+81-76-265-2235

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026