Skip to content

Study · Non-randomized trial · n = 7 · 1986

7 results

Treatment of autonomic neuropathy with a somatostatin analogue SMS-201-995.

Hoeldtke RD, O'Dorisio TM, Boden G

Lancet (London, England)1 Sept 1986Cited by 57 (Europe PMC)

Summary

The text of this summary is not shown here, because the article license does not allow reuse. Read it at the source (opens in a new tab)

Text rights: Publisher copyright. Results still quote short attributed sentences.

Results from this study7

7 results from studies that gave the peptide. 7 results from people.

  1. 01HumanNon-randomized trialEfficacy outcome

    SMS-201-995 raised upright postprandial blood pressure in five of seven patients with hypotension.

    In plain wordsSMS-201-995 raised upright blood pressure after meals in five of seven patients.

    Peptide
    Octreotide
    Outcome
    IncreaseUpright postprandial blood pressure
    Study

    n = 7

    Outcome group
    Blood pressure · Cardiovascular
    Studied dose
    up to 1.6 micrograms/kgAs given in this study (human).

    Measurements

    Patients with raised upright postprandial blood pressure
    5 patients
    doses up to 1.6 micrograms/kg

    Source sentences

    Summary
    Larger doses (up to 1.6 micrograms/kg) raised upright blood pressure during the postprandial period in five of seven patients.
    1 context sentence
    Summary · context
    Eight patients with postprandial hypotension and orthostatic hypotension were treated with the somatostatin analogue SMS-201-995.
  2. 02HumanNon-randomized trialEfficacy outcome

    In patients with postprandial hypotension, SMS-201-995 raised blood pressure after breakfast in all six patients.

    In plain wordsSMS-201-995 raised blood pressure after breakfast in all six patients with postprandial hypotension.

    Peptide
    Octreotide
    Outcome
    IncreasePostprandial blood pressure
    Study

    n = 6

    Outcome group
    Blood pressure · Cardiovascular
    Studied dose
    0.2-0.4 microgram/kgAs given in this study (human).

    Measurements

    Patients with raised postprandial blood pressure
    6 patients
    postprandial hypotension, 0.2-0.4 microgram/kg

    Source sentences

    Summary
    Low doses of this drug (0.2-0.4 microgram/kg) raised the blood pressure after breakfast in all six patients with postprandial hypotension.
    1 context sentence
    Summary · context
    Eight patients with postprandial hypotension and orthostatic hypotension were treated with the somatostatin analogue SMS-201-995.
  3. 03HumanNon-randomized trialEfficacy outcome

    Three patients unable to stand after eating could walk for 35-100 min after SMS-201-995 at breakfast.

    In plain wordsThree patients unable to stand after eating could walk for 35-100 min after SMS-201-995.

    Peptide
    Octreotide
    Outcome
    IncreaseAbility to walk after breakfast
    Study

    n = 3

    Comparator
    Before therapy
    Outcome group
    Exercise and physical function · Whole body
    Studied dose
    0.8 microgram/kg · injectionAs given in this study (human).

    Measurements

    Walking duration
    35 to 100 min
    after injection

    Source sentences

    Summary
    Before therapy three patients were unable to stand after eating; after an injection of SMS-201-995 0.8 microgram/kg at the beginning of breakfast they were able to walk for 35-100 min.
    1 context sentence
    Summary · context
    Eight patients with postprandial hypotension and orthostatic hypotension were treated with the somatostatin analogue SMS-201-995.
  4. 04HumanNon-randomized trialEfficacy outcome

    In patients with hypotension, sitting blood pressure after SMS-201-995 exceeded placebo by 35 +/- 10 mm Hg at 60 min after breakfast.

    In plain wordsIn patients with hypotension, SMS-201-995 raised sitting blood pressure more than placebo after breakfast.

    Peptide
    Octreotide
    Outcome
    IncreaseSitting blood pressure after breakfast
    Study

    n: not reported in source

    Comparator
    Placebo
    Outcome group
    Blood pressure · Cardiovascular
    Studied dose
    0.4 microgram/kgAs given in this study (human).

    Measurements

    Blood pressure difference
    35 mm Hg
    60 min after breakfast versus placebo
    SEM
    10 mm Hg
    blood pressure difference
    P value
    < 0.001
    versus placebo

    Source sentences

    Summary
    60 min after breakfast the mean sitting blood pressure was 35 +/- 10 (SEM) mm Hg higher after administration of SMS-201-995 0.4 microgram/kg than after placebo (p less than 0.001).
    1 context sentence
    Summary · context
    Eight patients with postprandial hypotension and orthostatic hypotension were treated with the somatostatin analogue SMS-201-995.
  5. 05HumanNon-randomized trialEfficacy outcome

    In patients with hypotension, each SMS-201-995 injection had a therapeutic effect lasting 3-6 h.

    In plain wordsIn patients with hypotension, each SMS-201-995 injection acted for 3-6 h.

    Peptide
    Octreotide
    Outcome
    Not applicableDuration of therapeutic effect
    Study

    n: not reported in source

    Outcome group
    Pharmacokinetics · Pharmacology
    Studied dose
    Dose not stated · injectionAs given in this study (human).

    Measurements

    Therapeutic effect duration
    3 to 6 h
    each injection

    Source sentences

    Summary
    The duration of therapeutic effect of each injection was 3-6 h.
    1 context sentence
    Summary · context
    Eight patients with postprandial hypotension and orthostatic hypotension were treated with the somatostatin analogue SMS-201-995.
  6. 06HumanNon-randomized trialSafety outcome

    Two patients with gastroparesis diabeticorum experienced abdominal cramps after SMS-201-995 treatment.

    In plain wordsTwo patients with diabetic gastroparesis experienced abdominal cramps after SMS-201-995 treatment.

    Peptide
    Octreotide
    Outcome
    Direction not reportedAbdominal cramps
    Study

    n: not reported in source

    Outcome group
    Gastrointestinal adverse events · Gastrointestinal
    Studied dose
    Dose not stated

    Measurements

    Patients with abdominal cramps
    2 patients
    patients with gastroparesis diabeticorum

    Source sentences

    Summary
    Treatment was followed by abdominal cramps and nausea in two patients with gastroparesis diabeticorum.
    1 context sentence
    Summary · context
    Eight patients with postprandial hypotension and orthostatic hypotension were treated with the somatostatin analogue SMS-201-995.
  7. 07HumanNon-randomized trialSafety outcome

    Two patients with gastroparesis diabeticorum experienced nausea after SMS-201-995 treatment.

    In plain wordsTwo patients with diabetic gastroparesis experienced nausea after SMS-201-995 treatment.

    Peptide
    Octreotide
    Outcome
    Direction not reportedNausea
    Study

    n: not reported in source

    Outcome group
    Gastrointestinal adverse events · Gastrointestinal
    Studied dose
    Dose not stated

    Measurements

    Patients with nausea
    2 patients
    patients with gastroparesis diabeticorum

    Source sentences

    Summary
    Treatment was followed by abdominal cramps and nausea in two patients with gastroparesis diabeticorum.
    1 context sentence
    Summary · context
    Eight patients with postprandial hypotension and orthostatic hypotension were treated with the somatostatin analogue SMS-201-995.

AI wrote and checked these results. AI can make mistakes, so check important results against the source.

Version history

PepBank keeps every version of the data on this study. Status changes from Retraction Watch, Europe PMC and Crossref are listed with their source.

  1. Version 2Current

    28 Oct 2026, 02:03 UTC

    Study results updated

  2. Version 1

    27 Oct 2026, 16:36 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

PepBank is a research reference. Talk to a doctor before you use any peptide.