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OpenTrials
Completed

NCT Number: NCT00909142

Bonefos and the Consumption of Analgesics

The effect of Bonefos on consumption of analgesics (drugs used for pain treatment) in patients with proven bone metastases.

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Key information

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Breast cancer or prostate cancer or multiple myeloma.
  • Bone metastasis.
  • Ability to use analgesics and clodronate 1600 mg/day.

Exclusion criteria

  • Hypersensitivity to bisphosphonates.
  • Clodronate in previous therapy.
  • Concomitant use of other bisphosphonates.
  • Serious renal insufficiency.

Treatment and study plan

Bonefos (Clodronate, BAY94-8393)

Drug

Patients in regular clinical practice receiving Bonefos according to local drug information

Primary outcomes

  1. Analgesics consumption after 12 months of treatment with Bonefos in patients with bone metastases and breast or prostate cancer or multiple myeloma

    Time frame: 12 months

Secondary outcomes

  1. Decrease in pain measured by VAS (Visual Analogue Scale)

    Time frame: 12 months

Sponsors and collaborators

Lead sponsor

Bayer

Industry

Registry information

Official study title

Bonefos and the Consumption of Analgesics. Influence of Clodronate on Analgesics Consumption Among Patients With Bone Metastasis

Acronym: BICAM

Important dates

Study start
2007
Primary completion
2009
Study completion
2009
First posted
May 27, 2009
Registry last updated
Apr 6, 2012

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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