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A Cohort Study on Obese Patients' Multidisciplinary Integrated Health Management

A Cohort Study on Obese Patients' Multidisciplinary Integrated Health Management

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07451938
Acronym
ODHM
Enrollment
1500
Registered
2026-03-05
Start date
2017-07-01
Completion date
2025-07-30
Last updated
2026-03-05

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

Conditions

Bariatric Surgery, Diabete Type 2, Obesity

Brief summary

To explore influencing factors of diabetes remission and recovery of other complications after bariatric surgery. We design a multicenter study including respective cohort and prorespective cohort of obese patients treated with bariatric surgery or non-bariatric surgery,and collect clinical parameters and laboratory indicators.

Interventions

PROCEDUREBariatric surgery

Laparoscopic sleeve gastrectomy or laparoscopic gastric bypass based on β-cell function

OTHERNon-surgical threapy

Diet management,exercise,metformin,GLP-1RA and other drugs which can lose weight.

Sponsors

China-Japan Friendship Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
12 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

1. Age range from 12 to 75 years, 2. BMI (Body Mass Index) ≥ 25.0 kg/m2,

Exclusion criteria

1. Type 1 diabetes, 2. Severe liver or kidney disease (eGFR \< 30 ml/min), malignant tumors, endocrine disorders such as thyroid or Cushing's syndrome, acute coronary syndrome, uncontrolled heart failure, pregnancy or lactation, pancreatitis, 3. Contraindications to other surgeries or medications.

Design outcomes

Primary

MeasureTime frame
Total weight loss1st, 3rd, 6th and 12th month after intervention, respectively.

Secondary

MeasureTime frame
Fasting blood glucose1st, 3rd, 6th and 12th month after intervention, respectively.
Average blood glucose from continuous glucose monitoring1st, 3rd, 6th and 12th month after intervention, respectively.
Postprandial 2-hour blood glucose1st, 3rd, 6th and 12th month after intervention, respectively.
HbA1c1st, 3rd, 6th and 12th month after intervention, respectively.
Waist circumference and hip circumference1st, 3rd, 6th and 12th month after intervention, respectively.
Medication status1st, 3rd, 6th and 12th month after intervention, respectively.
Quality of life score1st, 3rd, 6th and 12th month after intervention, respectively.
AHI1st, 3rd, 6th and 12th month after intervention, respectively.
GERDQ Score1st, 3rd, 6th and 12th month after intervention, respectively.
Urinary microalbumin1st, 3rd, 6th and 12th month after intervention, respectively.
Serum creatinine1st, 3rd, 6th and 12th month after intervention, respectively.
TC1st, 3rd, 6th and 12th month after intervention, respectively.
TG1st, 3rd, 6th and 12th month after intervention, respectively.

Countries

China

Contacts

PRINCIPAL_INVESTIGATORHua Meng

China-Japan Friendship Hospital

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 6, 2026