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Completed

NCT Number: NCT01293019

Osteopathic Treatment in Adult Patients With Cystic Fibrosis

To study the contribution of osteopathy on the reduction of pain in adult patients with cystic fibrosis

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Key information

Conditions

Cystic Fibrosis Back Pain Chest Pain Congenital, Hereditary, and Neonatal Diseases and Abnormalities Digestive System Diseases Genetic Diseases, Inborn Infant, Newborn, Diseases Lung Diseases Neck Pain Neurologic Manifestations Pain Pancreatic Diseases Pathological Conditions, Signs and Symptoms Respiratory Tract Diseases Signs and Symptoms

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Cochin Hospital

Paris, 75014, France

About this study

To compare the impact of osteopathic treatment to a placebo of osteopathic treatment and to usual care on pain at 6 months in adult patient with cystic fibrosis localized to chest, cervical, dorsal neck or back.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Diagnosis of cystic fibrosis ( positive sweat test and / or presence of 2 disease causing mutations in the CFTR gene
  • Age > 18 years
  • Patient with chronic chest , neck or back pain
  • Written Informed Consent
  • with health insurance

Exclusion criteria

  • regular follow-up by an osteopathic physician in the previous 3 months
  • patients awaiting lung transplantation
  • history of lung transplantation
  • pregnancy
  • understanding disorders preventing the patient to apply the study
  • participation in another clinical interventional study protocol

Treatment and study plan

Osteopathic treatment

Procedure

Real treatment of osteopathy

Other names: Real treatment of osteopathy

Sham Placebo

Procedure

Sham treatment of osteopathy

Other names: Sham treatment of osteopathy

usual care

Procedure

Classical treatment of pain in cystic fibrosis patients

Other names: Classical treatment of pain in cystic fibrosis patients

Primary outcomes

  1. Pain score

    Time frame: at 6 months

Secondary outcomes

  1. quality of life scores

    Time frame: at 6 months

  2. Co-interventions

    Time frame: at 6 months

Sponsors and collaborators

Lead sponsor

Assistance Publique - Hôpitaux de Paris

Other

Collaborators

  • URC-CIC Paris Descartes Necker Cochin
  • Vaincre la Mucoviscidose

Registry information

Official study title

Impact of an Osteopathic Manipulative Treatment on Pain of Adult Patients With Cystic Fibrosis - a Pilot Study

Acronym: MUCOSTEO

Important dates

Study start
2009
Primary completion
2011
Study completion
2011
First posted
Feb 10, 2011
Registry last updated
Jul 7, 2026

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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