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Effect of different doses of Polyethylene glycol Loose peptide on obesity in type 2 diabetic patients

Effect of different doses of Polyethylene glycol Loose peptide on obesity in type 2 diabetic patients

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200056789
Enrollment
Unknown
Registered
2022-02-17
Start date
2022-02-17
Completion date
Unknown
Last updated
2023-09-11

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

Conditions

Type 2 diabetes, obesity

Interventions

Without the Polyethylene glycol, Loose, the peptide:With the Polyethylene glycol, Loose, the peptide

Sponsors

Shandong Provincial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. (1999 WHO diagnostic criteria) confirmed type2 diabetes and GLP-1 indications (2017 version of CDA diagnosis and treatment guide) 2. only after diet adjustment and exercise treatment, or a stable dose oral hypoglycemic drug single medicine or two drug combination At least 3 months 3. 20-65 ye.ars old, gender unlimited 4. BMI19-35kg / m2, hba1c7.5 -11.0 5. fasting blood sugar 7.0-10.0mmol / L 6. sign informed consent 7. and strictly abide by clinical trial plan

Exclusion criteria

Exclusion criteria: 1. polyethylene glycol ropeptide injection skin test positive 2. has received GLP-1 agonist, DPP-4 inhibitor 3. hypertension history After the treatment of antihypertensive drugs, shrink pressure> 160mmHg and / or diastolic pressure> 100mmHg 4. serious cardiovascular disease patients 5. patients with diabetic ketoacid or nona keto hyperglycemia - hypertonic coma or severe hypoglycemia, patients with severe diabetes complications, patients with diabetes, monochrome mutant diabetes, 2 multiple Diabetes or secondary diabetes patients with endocrine injury, patients with pancreatic injury, human historic patients, inflammatory bowel disease and diabetic gastrointestinal paralysis patients, episodes of patients with pancreatitis, end-stage nephropathy Patients with severe liver function impaired (Glycoprine aminotransferase> 60 u / L or aspartate aminotransferase> 60U / L). 6. Data incomplete perspective, unwilling partners, pregnant women or lactating women 7 research adult can't complete research or bring obvious risks to subjects.

Design outcomes

Primary

MeasureTime frame
Fasting blood glucose;Blood sugar 2 hours after meal;Glycated hemoglobin;liver function;Renal function;Blood lipid;ß-hydroxybutyrate;C peptide;insulin;Glucagon;Urine microely protein than creatinine;Blood routine;Urinary routine;System measurement;Eye base;Islet function;

Secondary

MeasureTime frame
body weight;Waist circumference;Hip;Waist button ratio;Pleat thickness;blood pressure;Rhythm;Heart rate;Electrocardiogram;Carotid ultrasound;Abdominal ultrasound;Thyroid ultrasound;Echocardiography;Oxidative stress correlation index;

Countries

China

Contacts

Public ContactZhang Xiujuan
zhangxiujuan70732@126.com15168889691

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026