Patient Preferences, Analgesic Delivery Method and Pain Reduction in Spine Patients

Pain Relief Clinical Trial

Official title:

The Relationship Between Patient Preferences, Analgesic Delivery Method and Pain Reduction in Spine Patients

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT01263652
• Other study ID #: SpinePainIMPO
• Status: Withdrawn
• Phase: N/A
• Start date: December 31, 2010
• Est. completion date: June 1, 2019

Study information

• Verified date: May 2020
• Source: Western Galilee Hospital-Nahariya
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The investigators will conduct a randomized double blind study, to determine whether patient analgesic delivery mode preference affects pain reduction quality in non-surgical spine patients.

The patients will receive both intra-muscular and oral non-narcotic analgesics and placebo. During the study period, pain reduction parameters will be collected. At the end of the study period, the investigators will attempt to find a correlation between pre-study patient preferences and the quality of the pain reduction achieved.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: June 1, 2019
• Est. primary completion date: June 1, 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 15 Years to 100 Years

Eligibility

Inclusion Criteria:

• Patients with chronic and acute back pain

Exclusion Criteria:

• Recent Spine Surgery

Related Conditions & MeSH terms

• Pain Relief

Intervention

Drug:
• Diclofenac hydroxyethylpyrrolidine
IM/PO
• orphenadrine
IM/PO orphenadrine
• Tramadol
IM/PO tramadol
• Dipyrone
PO/IM Dipyrone

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Western Galilee Hospital-Nahariya

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	pain scores on visual analog scale	up to 7 days for each patient per hospitalization	visual analog scale will be mesuered before and one hour following every pain medication delivery
Secondary	Patient Questionnaire assessing pain and pain relief	A questionnaire will be filled immediately before and one hour following analgesic administration	Before administaration of pain control medication and one hour following analgesic administration
Secondary	patient preference Questionnaire	every patient will be asked for his prefered analgesic delivery method	before first analgesic administration at the current hositalization