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OpenTrials
Completed

NCT Number: NCT00696644

A Study for Teriparatide in Severe Osteoporosis

This observational study will evaluate the incidence of new vertebral and non vertebral fragility fractures in patients with severe osteoporosis treated with anabolic drugs. This study will also evaluate BMD, compliance to treatment, back pain and the health-related quality of life.

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Key information

Age range

21 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

For additional information regarding investigative sites for this study, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.

Valeggio sul Mincio, Verona, 36067, Italy

About this study

The participants should be treated with anabolic therapy for osteoporosis (Teriparatide or PTH 1-84) for 18 months and should be followed up for subsequent 6 months. The treatment is expected to improve bone mineral density, back pain and reduce the risk of new fractures due to osteoporosis. The outcomes will be evaluated by bone densitometry at the lumbar spine and femoral neck, by standard radiographs, by measurements of bone formation marker (P1NP) and by questionnaires on back pain and quality of life. Postmenopausal women and men over 21 years old may be included if they have:

  • at least 3 severe vertebral fractures
  • 2 severe vertebral fractures and 1 hip fracture
  • an incidental vertebral fracture or an hip fracture during treatment with antiresorptives prescribed for at least 12 months.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Postmenopausal women and men older than 21 years affected by severe osteoporosis with an incidental vertebral or hip fracture during treatment with an antiresorptive, or having 3 or more severe vertebral fractures or having 2 severe vertebral fractures and an historical hip fracture.

Exclusion criteria

  • Any contraindication for the use of antiosteoporotic drug
  • Premenopausal women or men younger than 21 years

Treatment and study plan

Teriparatide

Drug

20 mcg daily subcutaneous for 18 months.

Primary outcomes

  1. Incidence of any osteoporotic fractures in the first 24 months from the initiation of anabolic medication.

    Time frame: From 0 to 24 months

Secondary outcomes

  1. Treatment compliance

    Time frame: From 0 to 24 months

  2. Reason of discontinuation

    Time frame: From 0 to 24 months

  3. BMD changes (lumbar and femoral BMD)

    Time frame: From 0 to 24 months

  4. Changes in bone turnover marker measured by P1NP

    Time frame: From 0 to 24 months

  5. Quality of Life (measured by EQ-5D of EuroQol Group)

    Time frame: From 0 to 24 months

  6. Back Pain measured by visual analogue scale and back pain questionnaire

    Time frame: From 0 to 24 months

  7. Assessment of motor performance and chair rising test

    Time frame: From 0 to 24 months

Sponsors and collaborators

Lead sponsor

Eli Lilly and Company

Industry

Registry information

Official study title

An Italian Observational Study to Evaluate Fracture Outcomes, Compliance to Treatment, Back Pain, Health-related Quality of Life in Patients With Severe Osteoporosis Treated According to Common Clinical Practice

Acronym: ISSO

Important dates

Study start
2008
Primary completion
2011
Study completion
2011
First posted
Jun 13, 2008
Registry last updated
May 9, 2011

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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