NCT01403168

Comparative Evaluation of Osteopathy Treatment Efficacy in Pain Support After Breast Surgery in Oncology

• Status: Terminated
• Phase: N/A
• Study type: Interventional
• Enrollment: 28 (actual)
• Sponsor: Centre Leon Berard · Academic / Other
• Sex: Female
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

This is an open, prospective, controlled, randomized, comparative study with 2 arms. The purpose of the study is to assess the efficacy of osteopathy after breast surgery. 80 patients will be enrolled, 40 per arm. Patients will be randomized at inclusion and will be followed during one year.

Conditions

• Breast Cancer

Interventions

Type	Name	Description
OTHER	OSTEOPATHY + conventional analgesic treatments	5 sessions for osteopathy are planned and will start in the 15 days following the enrollment. The conventional analgesic treatments will be administered in the 15 days following the enrollment.
OTHER	Conventional analgesic treatments	These treatments will be administered in the 15 days following the enrollment. Dose and frequence will depend on patients.

Timeline

• Start date: 2011-04-01
• Primary completion: 2014-04-01
• Completion: 2015-04-01
• First posted: 2011-07-27
• Last updated: 2015-06-29

Locations

1 site across 1 country: France