Research on Optimal Strategy of Hypoglycemic Therapy for Cirrhosis With Diabetes

Sponsor
Huashan Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT05641337
Collaborator
(none)
184
1
2
39
4.7

Study Details

Study Description

Brief Summary

Poor blood glucose control in liver cirrhosis can aggravate the poor prognosis of patients. Under the background of the increasing number of liver cirrhosis patients with metabolic abnormalities, how to optimize treatment is particularly important. The traditional treatment of diabetes at the stage of liver cirrhosis is limited to insulin intensive therapy, but the incidence of hypoglycemia is high, blood sugar fluctuates greatly, and multiple injections are required. Research shows that insulin therapy has an increased overall mortality compared with non insulin therapy. We used metformin,Ryzodeg and an oral DDP IV enzyme inhibitor as the core combination according to the special pathological mechanism of elevated blood glucose in liver cirrhosis . After preliminary experiments, we found that the program was stable and was not easy to have hypoglycemia, and there was no traditional risk of lactic acid poisoning caused by metformin. We designed an open randomized controlled clinical study, Compared with the traditional insulin intensive treatment scheme, this new combination scheme was compared whether it could improve the blood glucose level, the incidence of hypoglycemia and lactic acid level, the incidence of cirrhosis complications, and the long-term survival rate of liver disease. This study is helpful to optimize the hypoglycemic treatment of cirrhosis with diabetes, and improve the blood glucose and long-term prognosis, The positive evidence of this study contributes to the consensus or guidelines for the treatment of cirrhosis with diabetes.

Condition or Disease Intervention/Treatment Phase
  • Drug: Insulin Degludec and Insulin Aspart
Phase 3

Detailed Description

Cirrhosis with diabetes refers to the increase of blood sugar in cirrhosis, including cirrhosis before or after diabetes. It has a special pathophysiological mechanism that liver factors participate in blood glucose regulation. Poor blood glucose control in liver cirrhosis can aggravate the poor prognosis of patients. Under the background of the increasing number of liver cirrhosis patients with metabolic abnormalities, how to optimize treatment is particularly important. The traditional treatment of diabetes at the stage of liver cirrhosis is limited to insulin intensive therapy, but the incidence of hypoglycemia is high, blood sugar fluctuates greatly, and multiple injections are required. Research shows that insulin therapy has an increased overall mortality compared with non insulin therapy. We used metformin, ,Ryzodeg and an oral DDP IV enzyme inhibitor as the core combination according to the special pathological mechanism of elevated blood glucose in liver cirrhosis from multiple links. After preliminary experiments, we found that the program was stable and was not easy to have hypoglycemia, and there was no traditional risk of lactic acid poisoning caused by metformin. We designed an open randomized controlled clinical study, Compared with the traditional insulin intensive treatment scheme, this new combination scheme was compared whether it could improve the blood glucose level, the incidence of hypoglycemia and lactic acid level, the incidence of cirrhosis complications, and the long-term survival rate of liver disease. This study is helpful to optimize the hypoglycemic treatment of cirrhosis with diabetes, and improve the blood glucose and long-term prognosis of such patients, The positive evidence of this study contributes to the consensus or guidelines for the treatment of cirrhosis with diabetes.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
184 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Research on Optimal Strategy of Hypoglycemic Therapy for Cirrhosis With Diabetes
Actual Study Start Date :
Oct 1, 2022
Anticipated Primary Completion Date :
Dec 30, 2025
Anticipated Study Completion Date :
Dec 30, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: group with new combination therapy

The hypoglycemic scheme of the experimental group was that the initial dose of Insulin Degludec and Insulin Aspart was 0.3U/kg multiplied by the patient's weight, plus 5 mg of linagliptin and 0.5 g of metformin three times a day.

Drug: Insulin Degludec and Insulin Aspart
The hypoglycemic scheme of the experimental group was that the initial dose of Insulin Degludec and Insulin Aspart was 0.3U/kg multiplied by the patient's weight, plus 5 mg of linagliptin and 0.5 g of metformin three times a day. The control group was treated with traditional four needle insulin.
Other Names:
  • metformin
  • linagliptin
  • Active Comparator: group with intensive insulin therapy

    group was treated with intensive insulin therapy.The initial total amount of insulin is 0.5U/kg, of which 40% is basal insulin and 20% is aspart insulin before three meals

    Drug: Insulin Degludec and Insulin Aspart
    The hypoglycemic scheme of the experimental group was that the initial dose of Insulin Degludec and Insulin Aspart was 0.3U/kg multiplied by the patient's weight, plus 5 mg of linagliptin and 0.5 g of metformin three times a day. The control group was treated with traditional four needle insulin.
    Other Names:
  • metformin
  • linagliptin
  • Outcome Measures

    Primary Outcome Measures

    1. time in range [two weeks]

      time in range

    2. Blood lactic acid level [two week]

      Blood lactic acid level

    3. Compound adverse events [two week]

      includetimes of hypolgycemia attackļ¼Œsevere hypoglycemia attack and serum lactic acid more than 2.2 mmol/L, complications of liver cirrhosis within two week

    Secondary Outcome Measures

    1. mean blood glucose [two weeks]

      mean blood glucose

    2. Time above range [two weeks]

      Time above range

    3. Time below range [two weeks]

      Time below range

    4. Blood lactic acid [two weeks]

      Blood lactic acid

    5. Glycated Albumin [two week]

      Glycated Albumin

    6. three month mortality [three months]

      three month mortality

    7. Six month mortality [six months]

      Six month mortality

    8. Incidence rate of complications of liver cirrhosis within three months [three months]

      Incidence rate of complications of liver cirrhosis within three months

    9. Incidence rate of complications of liver cirrhosis within six months [six months]

      Incidence rate of complications of liver cirrhosis within six months

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 70 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Liver cirrhosis

    • Age 18-70 years

    • Patients with elevated blood sugar who meet the diabetes standard or have been treated with hypoglycemic drugs

    • random finger or venous serum blood glucose more than 14 mmol/L

    Exclusion Criteria:
    • Those unwilling to participate or unable to cooperate;

    • Child-pugh score is greater than 12;

    • Glomerular filtration rate<60ml/min/1.73m2;

    • Patients with cardiac insufficiency;

    • Patients with asymptomatic hypoglycemia;

    • Pregnant patients were excluded;

    • Patients with advanced liver cancer;

    • Blood pressure is less than 90/60mmHg;

    • Chronic liver disease plus acute or subacute liver failure;

    • Patients with drug induced blood glucose disorder, such as glucocorticoids, contraceptives, etc;

    • fingertip oxygen saturation less than 95% without oxygen inhalation;

    • Autoimmune liver cirrhosis is currently taking hormone.

    • Type 1 diabetes.

    • Pancreatogenic diabetes, such as primary hemochromatosis, hepatolenticular degeneration, alcoholic pancreatitis, autoimmune diseases involving the pancreas, etc.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Xiaolong Zhao Shanghai Shanghai China 200041

    Sponsors and Collaborators

    • Huashan Hospital

    Investigators

    • Study Chair: Xiaolong Zhao, PhD, Shanghai Public Health Clinical Center

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    xiaolong zhao, Chief Physician, Huashan Hospital
    ClinicalTrials.gov Identifier:
    NCT05641337
    Other Study ID Numbers:
    • 2022-10-cirrhosis with DM
    First Posted:
    Dec 7, 2022
    Last Update Posted:
    Dec 7, 2022
    Last Verified:
    Nov 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by xiaolong zhao, Chief Physician, Huashan Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Dec 7, 2022