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Effect of Hyperglycemia on Gastric Emptying Interactions With Pramlintide

15. januar 2008 opdateret af: Ludwig-Maximilians - University of Munich

The Influence of Ambient Glycemia on the Effect of Pramlintide on Gastric Emptying in Patients With Type 1 Diabetes and Healthy Subjects

• To examine the influence of acute glycaemia (normoglycaemia and hyperglycaemia) on gastric emptying kinetics in patients with type 1 diabetes and non diabetic subjects when treated with subcutaneous (SC) injections of pramlintide.

Studieoversigt

Detaljeret beskrivelse

Postprandial increases in plasma glucose concentrations are mainly determined by the degree of postprandial suppression of endogenous glucose production and the rate of appearance of the ingested glucose. The latter is predominantly determined by the amount of glucose taken up by the splanchnic bed. Because nutrient absorption depends on gastric nutrient delivery, gastric emptying rate is a key determinant of the early rise of plasma glucose postprandially. At mealtime, the faster the stomach empties the more rapid the rise in plasma glucose. Yet, plasma glucose concentration is a determinant of gastric emptying rate. In non-diabetic subjects, as plasma glucose rises and approaches the upper limit of the normal range (~140 mg/dl), gastric emptying slows. This likely represents a physiological brake mechanism to limit excess delivery of nutrients, thus avoiding excessive appearance of glucose in plasma. In diabetes, abnormally accelerated gastric emptying as well as delayed gastric emptying have been reported. These conflicting data may be explained by differences of ambient glycaemia. In most of these studies undertaken in diabetic subjects these patients were severely hyperglycaemic, thus the reported delayed gastric emptying may be explained by the effect of hyperglycaemia on gastric motility. Indeed, a small number of studies controlled for ambient glycaemia found acceleration of gastric emptying in diabetes and suggest that diabetes manifests with a maladaptive acceleration of gastric emptying likely contributing to excessive postprandial plasma glucose excursions.

The amylin analog pramlintide is a potential new therapeutic that elicits a potent glucose lowering effect in the postprandial period thought to be due to both a suppression of plasma glucagon and a delay of gastric emptying. It is not clear, however, to what extent the pramlintide-induced delay of gastric emptying offsets a potential maladaptive acceleration of gastric emptying in diabetes patients studied under controlled glycemic conditions. In theory, every drug that reduces hyperglycaemia should accelerate gastric emptying and, thereby, minimize its potential effect on postprandial hyperglycaemia. Thus, the drug-induced effect of amylin on gastric motility may be of great advantage by offset the effects of glycemic induced acceleration on gastric emptying.

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

27

Fase

  • Ikke anvendelig

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

18 år til 65 år (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ja

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

All of the following criteria are to be fulfilled for inclusion of an individual in the study unless the investigator grants an exception:

  • Clinical diagnosis of type 1 diabetes (otherwise healthy) with an HbA1 ≤ 9%, and on a stable insulin treatment for at least 3 months (preferably on pump regimen) prior to screening OR is a healthy individual.
  • 20-40 years of age, inclusive.
  • Understand and sign an informed consent document, communicate with the investigator, and understand and comply with the requirements of the study.
  • Euthyroid, including subjects receiving thyroid replacement therapy.

If female:

  • Is surgically sterilized by hysterectomy; OR
  • Is post-menopausal, as documented by a history of amenorrhea for 6 months and follicle stimulating hormone (FSH) level within the range specified as post-menopausal by the reporting laboratory at screen (post menopausal women on estrogen may enter the study without obtaining an FSH level); OR
  • If of childbearing potential, meets the following criteria:

negative pregnancy test (ß-HCG), regardless of birth control method (including subjects with tubal ligation);

  • Practicing and willing to continue throughout the study the appropriate contraception (defined as oral, injected, or implanted contraceptives for at least 3 months prior to entry, or barrier contraception).
  • Agree to take every precaution to ensure that pregnancy will not occur during the study.

Exclusion Criteria:

  • Individuals meeting any of the following criteria are to be excluded from the study unless the investigator grants an exception:
  • History of severe hypoglycemia.
  • Body mass index (BMI) ≥ 30 kg/m2.
  • Autonomic nerve dysfunction: abnormal result in the cardiovascular parasympathetic and/or sympathetic tests (screening visit).

Hepatic disease:

  • Known hepatic disease or transaminases (GOT, GPT) ≥ 2x above normal values.

Renal disease:

  • Known or serum urea, serum creatinine ≥ 1.5x above normal values
  • Cardiovascular or pulmonary disease:
  • Arterial hypertension
  • Blood pressure >150/95 mmHg at screening in a sitting position)
  • Arterial occlusive disease
  • Known coronary heart disease
  • Abnormal ECG at screening visit.
  • Gastrointestinal disease:
  • Any known structural gastrointestinal disorder,
  • Gastrointestinal surgery except for appendectomy,
  • Symptoms indicating functional or structural upper gastrointestinal disorder (pain, bloating, postprandial fullness, nausea, emesis,
  • Gastroectomy, gastroparesis, lactose intolerance, and diseases known to alter small bowel absorption; e.g., inflammatory bowel disease.

CNS disease:

  • Epilepsy (including subjects with a past history of convulsions associated with hypoglycaemia),
  • Psychiatric illness (including history of eating disorder such as bulimia or anorexia).
  • Autoimmune disease other than thyroid, pernicious anemia, or vitiligo.
  • Malignant disease requiring chemotherapy,
  • Any acute febrile illness within 2 weeks of Screening (Visit 1) with a temperature of 100°F,
  • Currently abusing alcohol or drugs, or have a history of alcohol or drug abuse that in the investigator's opinion could cause the subject to be non-compliant; or have a general history of non-compliance with medications.
  • Receipt of any investigational drug within 90 days of Screening (Visit 1) (prior treatment with pramlintide is permissible).
  • Currently treated with medications known to interfere with gastric emptying such as, but not limited to:

    • Ca2+ channel antagonists, ß-receptor antagonists, prokinetic agents metoclopramide (Reglan®) and cisapride (Propulsid®); and
    • Chronic (more than 10 days within a 6-month period) macrolide antibiotics such as erythromycin and newer derivatives.
  • Currently treated with:

    • Bile acid sequestering resins cholestyramine (Questran®) and colestipol (Colestid®),
    • Systemic steroids,
    • Anti-obesity agents (including orlistat [Xenical®] and sibutramine [Meridia®]),
    • Alpha-glucosidase inhibitors (acarbose [Precose®] and miglitol [Glyset®]) and meglitinides ([Prandin®] and [Starlix®]).

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Diagnostisk
  • Tildeling: Randomiseret
  • Interventionel model: Crossover opgave
  • Maskning: Enkelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Placebo komparator: 1
Placebo, euglycemia
placebo SC during euglycemia
placebo during hyperglycemia
Eksperimentel: 2
Pramlintide, euglycemia
pramlintide SC during eglycemia
pramlintide SC during hyperglycemia
Placebo komparator: 3
placebo, hyperglycemia
placebo SC during euglycemia
placebo during hyperglycemia
Eksperimentel: 4
pramlintide, hyperglycemia
pramlintide SC during eglycemia
pramlintide SC during hyperglycemia

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Tidsramme
• To examine the influence of acute glycaemia (normoglycaemia and hyperglycaemia) on gastric emptying kinetics in patients with type 1 diabetes and non diabetic subjects when treated with subcutaneous (SC) injections of pramlintide.
Tidsramme: 2 years
2 years

Sekundære resultatmål

Resultatmål
Tidsramme
• Gastric peristalsis derived from high-resolution scintigraphy by means of Fast Fourier Transform (FFT) analysis. • Effects on gastric emptying and on the rate of appearance of ingested glucose appearance, postprandial glucose sequestration, endoge
Tidsramme: 2 years
2 years

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Samarbejdspartnere

Efterforskere

  • Ledende efterforsker: Joerg Schirra, MD, Ludwig-Maximilians-University of Munic

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart

1. januar 2005

Primær færdiggørelse (Faktiske)

1. marts 2007

Studieafslutning (Faktiske)

1. april 2007

Datoer for studieregistrering

Først indsendt

19. juni 2007

Først indsendt, der opfyldte QC-kriterier

19. juni 2007

Først opslået (Skøn)

21. juni 2007

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Skøn)

16. januar 2008

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

15. januar 2008

Sidst verificeret

1. januar 2008

Mere information

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

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