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Impact of Hypoglycemia Unawareness on Brain Metabolism Cognition in T1DM

31 marzo 2020 aggiornato da: Yale University
The research study is designed to examine the impact of low blood sugar on brain function in individuals with Type 1 Diabetes who have frequent and severe hypoglycemia (low blood sugar) compared to those who do not.

Panoramica dello studio

Stato

Completato

Descrizione dettagliata

During the course of treating diabetes (for example, after an insulin injection), blood sugar levels will sometimes drop too low. This condition is known as hypoglycemia. Normally, a healthy body responds to hypoglycemia by producing a number of "anti-insulin" hormones which raise blood sugar levels. In addition, these hormones provide the individual with warning signals of hypoglycemia, including hunger, sweating, shaking and heart palpitations. These warning signals allow diabetics to correct low blood sugar levels by eating sugar tablets or by having a snack.

Unfortunately, and for unclear reasons, many people with longstanding diabetes lose their ability to recognize low blood sugar levels-a condition called "hypoglycemia unawareness." The brain, in particular, is extremely sensitive to hypoglycemia. Unable to sense and respond to low blood sugar levels, these individuals may experience a sudden onset of blurred vision, confusion, seizures, coma, or even death.

In recent years, a new technique called "islet cell transplantation" has been developed as an alternate means of treating insulin-dependent diabetes. Pancreatic islet cells (the cells that produce insulin), from human donors, are injected into the diabetic patient's liver where the cells are capable of making insulin and can regulate blood sugar levels without the need for insulin injections. Currently, this technique is used primarily in patients with severe hypoglycemia unawareness.

While it is known that islet cell transplantation can reduce the risk of severe hypoglycemia, the effects of transplantation on hypoglycemia unawareness are unknown. This study is designed to investigate why hypoglycemia unawareness happens and the impact it has on brain function in individuals with type 1 diabetes.

Tipo di studio

Osservativo

Iscrizione (Anticipato)

51

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

    • Connecticut
      • New Haven, Connecticut, Stati Uniti, 06520
        • Yale University School of Medicine

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

Da 18 anni a 49 anni (Adulto)

Accetta volontari sani

Sessi ammissibili allo studio

Tutto

Metodo di campionamento

Campione non probabilistico

Popolazione di studio

Group 1A) T1DM subjects with severe hypoglycemia unawareness and awaiting islet cell transplantation will be referred by participating islet transplantation centers.

Group 1B) T1DM subjects with severe hypoglycemia unawareness but not awaiting islet cell transplantation will be from the greater New Haven, CT area.

Group 2)T1DM, not optimally controlled and without hypoglycemia unawareness will be from the greater New Haven, CT area.

Group 3) Non-Diabetics from the greater New Haven CT area.

Descrizione

Inclusion Criteria:

  • Inclusion Criteria for all subjects:

    • Age 18-49
    • > 85 kg
    • BMI <27female <28 male
    • able to provide written informed consent
    • able to speak and read English fluently
    • must meet Magnetic Resonance safety evaluation

Inclusion criteria for Group 1A:

  • T1DM undergoing intensive clinical management and currently on the islet transplant list
  • History of severe hypoglycemia

Inclusion criteria for Group 1B:

  • T1DM undergoing intensive clinical management
  • History of severe hypoglycemia unawareness

Inclusion criteria for Group 2:

  • T1DM with poor glycemic control, HbA1c > 8%
  • no episodes of hypoglycemia requiring assistance from another person for at least 1 yr, no episodes in last 4 weeks, and hypoglycemia aware

Exclusion Criteria:

Group 1A: (T1DM subjects being considered for islet cell transplantation)

  • Detectable c-peptide level
  • Untreated proliferative retinopathy
  • Creatinine clearance < 65 ml/min/1.73 m2
  • Serum creatinine ≥1.5 mg/dL
  • Previous pancreas or islet transplant
  • Positive pregnancy test, or presently breast-feeding, or failure to follow effective contraceptive measures
  • Active infection including hepatitis C, hepatitis B, HIV, or TB (or under treatment for suspected TB ), or subjects with a positive PPD performed within 1 yr. of enrollment, and no history of adequate prophylaxis
  • Invasive aspergillus infection within year prior to study entry
  • Any history of malignancy except for adequately treated squamous or basal cell carcinoma of the skin
  • Active alcohol or substance abuse- includes cigarette smoking (must be abstinent for 6 months)
  • History of non-adherence to prescribed regimens
  • Psychiatric disorder making the subject not a suitable candidate for transplantation
  • Baseline Hgb < 10.5 g/dL in females, or < 13 g/dL in males; lymphopenia (<1,000/μL), or leukopenia (< 3,000 total leukocytes/μL), or an absolute CD4+ count < 500/μL
  • History of coagulopathy or medical condition requiring long-term anticoagulant therapy (e.g., warfarin) after transplantation (low-dose aspirin treatment is allowed) or patient with INR >1.5
  • Severe co-existing cardiac disease, as determined by referring center
  • Baseline liver function tests outside of normal range (an initial liver function test panel with any values >1.5 times normal upper limits will exclude a patient without a re-test; a re-test for any values between normal and 1.5 times normal will be made, and if the values remain elevated above normal, the patient will be excluded), or history of significant liver disease
  • Severe unremitting diarrhea or other gastrointestinal disorders potentially interfering with the ability to absorb oral medications
  • Addison's disease as determined by clinical history
  • Under treatment for a medical condition requiring chronic use of systemic steroids
  • Any medical condition or medication that, in the opinion of the investigators, will interfere with the safe completion of the study or study outcomes

Group 1 B: (T1DM with Severe Hypoglycemia Unawareness not on the Transplant List)

  • Detectable C-peptide level
  • Serum creatinine ≥1.5 mg/dL
  • Positive pregnancy test, or presently breast-feeding, or failure to follow effective contraceptive measures
  • Active alcohol or substance abuse- includes cigarette smoking (must be abstinent for 6 months)
  • Psychiatric disorder making the subject not a suitable candidate for transplantation
  • Baseline Hgb < 10.5 g/dL in females, or < 13 g/dL in males
  • Baseline liver function tests outside of normal range (an initial liver function test panel with any values >1.5 times normal upper limits will exclude a patient without a re-test; a re-test for any values between normal and 1.5 times normal will be made, and if the values remain elevated above normal, the patient will be excluded), or history of significant liver disease
  • Under treatment for a medical condition requiring chronic use of systemic steroids
  • Any medical condition or medication that, in the opinion of the investigators, will interfere with the safe completion of the study or study outcomes

Group 2: (T1DM control subjects)

  • Detectable C-peptide level
  • Serum creatinine ≥1.5 mg/dL
  • Positive pregnancy test, or presently breast-feeding, or failure to follow effective contraceptive measures
  • Any history of malignancy except for adequately treated squamous or basal cell carcinoma of the skin
  • Active alcohol or substance abuse- includes cigarette smoking (must be abstinent for 6 months)
  • Baseline Hgb < 10.5 g/dL in females, or < 13 g/dL in males Baseline liver function tests outside of normal range (an initial liver function test panel with any values >1.5 times normal upper limits will exclude a patient without a re-test; a re-test for any values between normal and 1.5 times normal will be made, and if the values remain elevated above normal, the patient will be excluded), or history of significant liver disease
  • Addison's disease as determined by clinical history
  • Under treatment for a medical condition requiring chronic use of systemic steroids
  • Any medical condition or medication that, in the opinion of the investigators, will interfere with the safe completion of the study or study outcomes

Group 3: (Normal Controls)

  • FBG > 100 mg/dL
  • Serum creatinine ≥1.5 mg/dL
  • Positive pregnancy test, or presently breast-feeding, or failure to follow effective contraceptive measures
  • Any history of malignancy except for adequately treated squamous or basal cell carcinoma of the skin
  • Active alcohol or substance abuse- includes cigarette smoking (must be abstinent for 6 months)
  • Baseline Hgb < 10.5 g/dL in females, or < 13 g/dL in males
  • Baseline liver function tests outside of normal range (an initial liver function test panel with any values >1.5 times normal upper limits will exclude a patient without a re-test; a re-test for any values between normal and 1.5 times normal will be made, and if the values remain elevated above normal, the patient will be excluded), or history of significant liver disease
  • Under treatment for a medical condition requiring chronic use of systemic steroids
  • Any medical condition or medication that, in the opinion of the investigators, will interfere with the safe completion of the study or study outcomes

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

Coorti e interventi

Gruppo / Coorte
1A, 1B

Type 1 diabetic subjects with a history of severe hypoglycemia and hypoglycemia unawareness who:

1A) meet criteria for islet cell transplantation and are referred by a participating islet cell transplantation center

1B) meet similar criteria but are not currently planning islet cell transplantation

2
Type 1 diabetics who are not optimally controlled (>8% HbA1c) and rarely experience hypoglycemia
3
Healthy non-diabetics

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Investigatori

  • Investigatore principale: Robert Sherwin, MD, Yale University

Pubblicazioni e link utili

La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio

1 agosto 2005

Completamento dello studio (Effettivo)

1 agosto 2008

Date di iscrizione allo studio

Primo inviato

14 dicembre 2007

Primo inviato che soddisfa i criteri di controllo qualità

17 dicembre 2007

Primo Inserito (Stima)

18 dicembre 2007

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

2 aprile 2020

Ultimo aggiornamento inviato che soddisfa i criteri QC

31 marzo 2020

Ultimo verificato

1 marzo 2020

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • 0505000077_B
  • R01DK072409 (Sovvenzione/contratto NIH degli Stati Uniti)
  • HIC# 0505000077

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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