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Study · Randomized controlled trial · 1995

6 results

A double-blind, placebo-controlled, dose-finding trial of intermittent nasal salmon calcitonin for prevention of postmenopausal lumbar spine bone loss.

Reginster JY, Deroisy R, Lecart MP, Sarlet N, Zegels B, Jupsin I, de Longueville M, Franchimont P

The American journal of medicine1 May 1995Cited by 56 (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 study6

6 results from studies that gave the peptide. 6 results from people.

  1. 01HumanRandomized controlled trialEfficacy outcome

    In early postmenopausal women, combined salmon calcitonin groups had significantly better lumbar spine BMD evolution than placebo.

    In plain wordsIn early postmenopausal women, spine bone density changed more favorably with combined salmon calcitonin groups than placebo.

    Outcome
    IncreaseLumbar spine BMD change versus placebo
    Study

    n: not reported in source

    Comparator
    Placebo
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    50 or 200 IU/day on 5 consecutive days per week · intranasalAs given in this study (human).

    Measurements

    P
    0.0001
    between groups

    Source sentences

    Summary
    The difference between the evolution of the combined groups receiving nasal SCT and the group treated with the placebo was highly significant (P = 0.0001).
    4 context sentences
    Summary · context
    We performed a double-blind, placebo-controlled, randomized, single-center study with a 3-arm parallel-group design.
    Summary · context
    The subjects were 251 healthy women who had experienced natural menopause within the past 6 to 72 months and were not affected by any diseases or treatments that interfere with calcium metabolism.
    Summary · context
    They were randomly allocated in groups of 6 to receive intranasal SCT 50 IU (n = 84), SCT 200 IU (n = 84), or placebo (n = 83).
    Summary · context
    All treatments were given on 5 consecutive days per week.
  2. 02HumanNon-randomized trialEfficacy outcome

    In early postmenopausal women, lumbar spine BMD changed by 0.82% with salmon calcitonin, without significant change from baseline.

    In plain wordsIn early postmenopausal women, spine bone density did not change significantly from baseline with salmon calcitonin.

    Outcome
    No significant changeLumbar spine BMD, intention-to-treat
    Study

    n: not reported in source

    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    50 IU/day on 5 consecutive days per week · intranasalAs given in this study (human).

    Measurements

    BMD change
    0.82%
    IT
    95% CI lower
    −0.26%
    IT
    95% CI upper
    1.89%
    IT

    Source sentences

    Summary
    LSBMD increased slightly with the 50-IU/d dose of SCT, by 0.82% (95% CI -0.26 to 1.89) in the IT population, and 0.51% (95% CI -0.69 to 1.72) in the VC (P = NS, versus baseline).
    4 context sentences
    Summary · context
    We performed a double-blind, placebo-controlled, randomized, single-center study with a 3-arm parallel-group design.
    Summary · context
    The subjects were 251 healthy women who had experienced natural menopause within the past 6 to 72 months and were not affected by any diseases or treatments that interfere with calcium metabolism.
    Summary · context
    They were randomly allocated in groups of 6 to receive intranasal SCT 50 IU (n = 84), SCT 200 IU (n = 84), or placebo (n = 83).
    Summary · context
    All treatments were given on 5 consecutive days per week.
  3. 03HumanNon-randomized trialEfficacy outcome

    In early postmenopausal women who completed treatment, lumbar spine BMD changed by 0.51% with salmon calcitonin, without significant change from baseline.

    In plain wordsIn early postmenopausal completers, spine bone density did not change significantly from baseline with salmon calcitonin.

    Outcome
    No significant changeLumbar spine BMD, valid completers
    Study

    n: not reported in source

    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    50 IU/day on 5 consecutive days per week · intranasalAs given in this study (human).

    Measurements

    BMD change
    0.51%
    VC
    95% CI lower
    −0.69%
    VC
    95% CI upper
    1.72%
    VC

    Source sentences

    Summary
    LSBMD increased slightly with the 50-IU/d dose of SCT, by 0.82% (95% CI -0.26 to 1.89) in the IT population, and 0.51% (95% CI -0.69 to 1.72) in the VC (P = NS, versus baseline).
    4 context sentences
    Summary · context
    We performed a double-blind, placebo-controlled, randomized, single-center study with a 3-arm parallel-group design.
    Summary · context
    The subjects were 251 healthy women who had experienced natural menopause within the past 6 to 72 months and were not affected by any diseases or treatments that interfere with calcium metabolism.
    Summary · context
    They were randomly allocated in groups of 6 to receive intranasal SCT 50 IU (n = 84), SCT 200 IU (n = 84), or placebo (n = 83).
    Summary · context
    All treatments were given on 5 consecutive days per week.
  4. 04HumanNon-randomized trialEfficacy outcome

    In early postmenopausal women, salmon calcitonin increased lumbar spine BMD by 2.03% from baseline in the intention-to-treat population.

    In plain wordsIn early postmenopausal women, salmon calcitonin increased spine bone density from baseline.

    Outcome
    IncreaseLumbar spine BMD, intention-to-treat
    Study

    n: not reported in source

    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    200 IU/day on 5 consecutive days per week · intranasalAs given in this study (human).

    Measurements

    BMD change
    2.03%
    IT
    95% CI lower
    0.92%
    IT
    95% CI upper
    3.15%
    IT
    P
    0.001
    IT

    Source sentences

    Summary
    Subjects who received SCT 200 IU/d experienced significant increases of 2.03% (95% CI 0.92 to 3.15) in the IT population and 2.26% (95% CI 1.01 to 3.51) in the VC (both P = 0.001).
    4 context sentences
    Summary · context
    We performed a double-blind, placebo-controlled, randomized, single-center study with a 3-arm parallel-group design.
    Summary · context
    The subjects were 251 healthy women who had experienced natural menopause within the past 6 to 72 months and were not affected by any diseases or treatments that interfere with calcium metabolism.
    Summary · context
    They were randomly allocated in groups of 6 to receive intranasal SCT 50 IU (n = 84), SCT 200 IU (n = 84), or placebo (n = 83).
    Summary · context
    All treatments were given on 5 consecutive days per week.
  5. 05HumanNon-randomized trialEfficacy outcome

    In early postmenopausal completers, salmon calcitonin increased lumbar spine BMD by 2.26% from baseline.

    In plain wordsIn early postmenopausal completers, salmon calcitonin increased spine bone density from baseline.

    Outcome
    IncreaseLumbar spine BMD, valid completers
    Study

    n: not reported in source

    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    200 IU/day on 5 consecutive days per week · intranasalAs given in this study (human).

    Measurements

    BMD change
    2.26%
    VC
    95% CI lower
    1.01%
    VC
    95% CI upper
    3.51%
    VC
    P
    0.001
    VC

    Source sentences

    Summary
    Subjects who received SCT 200 IU/d experienced significant increases of 2.03% (95% CI 0.92 to 3.15) in the IT population and 2.26% (95% CI 1.01 to 3.51) in the VC (both P = 0.001).
    4 context sentences
    Summary · context
    We performed a double-blind, placebo-controlled, randomized, single-center study with a 3-arm parallel-group design.
    Summary · context
    The subjects were 251 healthy women who had experienced natural menopause within the past 6 to 72 months and were not affected by any diseases or treatments that interfere with calcium metabolism.
    Summary · context
    They were randomly allocated in groups of 6 to receive intranasal SCT 50 IU (n = 84), SCT 200 IU (n = 84), or placebo (n = 83).
    Summary · context
    All treatments were given on 5 consecutive days per week.
  6. 06HumanNon-randomized trialEfficacy outcome

    In early postmenopausal women, biochemical bone turnover parameters showed no significant changes during the study.

    In plain wordsIn early postmenopausal women, biochemical measures of bone turnover did not change significantly during the study.

    Outcome
    No significant changeBiochemical bone turnover parameters
    Study

    n: not reported in source

    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    50 or 200 IU/day on 5 consecutive days per week · intranasalAs given in this study (human).

    Source sentences

    Summary
    No significant changes were recorded in biochemical parameters reflecting bone turnover.
    5 context sentences
    Summary · context
    The main assessments performed were bone mineral density of the lumbar spine (LSBMD) and biochemical parameters reflecting bone turnover (serum alkaline phosphatase, urinary calcium/creatinine, and hydroxyproline/creatinine ratios).
    Summary · context
    We performed a double-blind, placebo-controlled, randomized, single-center study with a 3-arm parallel-group design.
    Summary · context
    The subjects were 251 healthy women who had experienced natural menopause within the past 6 to 72 months and were not affected by any diseases or treatments that interfere with calcium metabolism.
    Summary · context
    They were randomly allocated in groups of 6 to receive intranasal SCT 50 IU (n = 84), SCT 200 IU (n = 84), or placebo (n = 83).
    Summary · context
    All treatments were given on 5 consecutive days per week.

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, 16:35 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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